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Sep 23, 2024

Franklin Lakes, NJ

|

Laboratory Technician

|

Contract

|

$26 - $33 (hourly estimate)

{"JobID":382379,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.1944636363636,"Longitude":41.0289181818182,"Distance":null},"State":"New Jersey","Zip":"07417","ReferenceID":"HTS-736133","PostedDate":"\/Date(1727108071000)\/","Description":"Insight Global is looking for a Clinical Lab Specialist for our Life Sciences and Med Device client in Franklin Lakes, NJ. This role will include the following:- Design, evaluate, execute, and report on the safety and efficacy of in-vitro diagnostic devices.- Conduct clinical testing and manage laboratory studies and complaint testing.- Develop and implement new testing methodologies in collaboration with R\u0026D.- Perform Clinical Software Validations (CSV) and instrument validation/qualification.- Maintain laboratory instrumentation and reagent test systems.- Implement and document Quality Assurance and Quality Control procedures.- Train new associates and stay current in Clinical Laboratory Science through continuing education.- Resolve customer complaints through clinical investigations.- Support innovation, product development, clinical testing, manufacturing, and post-market surveillance.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Clinical Lab Specialist","City":"Franklin Lakes","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- 1-5+ years in a Clinical Laboratory environment - Strong knowledge of clinical laboratory science.- Excellent verbal and written communication skills.- Experience testing medical instruments (syringes, catheters, etc) - Experience processing specimens within the hematology, clinical chemistry, and urinalysis spaces - Awareness of GCP/GLP and ISO regulations.- Experience with human blood specimen collection products.- Strong computer skills and project planning/budget management skills.- BS/BA/MA in Clinical Laboratory Science, Medical Technology, Biology Life Sciences, or a related health field.","Skills":"- MT/MLT CLS (ASCP) or equivalent experience in a research environment.","Industry":"Laboratory Technician","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":33.0000,"SalaryLow":26.4000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is looking for a Clinical Lab Specialist for our Life Sciences and Med Device client in Franklin Lakes, NJ. This role will include the following:- Design, evaluate, execute, and report... on the safety and efficacy of in-vitro diagnostic devices.- Conduct clinical testing and manage laboratory studies and complaint testing.- Develop and implement new testing methodologies in collaboration with R&D.- Perform Clinical Software Validations (CSV) and instrument validation/qualification.- Maintain laboratory instrumentation and reagent test systems.- Implement and document Quality Assurance and Quality Control procedures.- Train new associates and stay current in Clinical Laboratory Science through continuing education.- Resolve customer complaints through clinical investigations.- Support innovation, product development, clinical testing, manufacturing, and post-market surveillance.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Sep 16, 2024

Philadelphia, PA

|

Nurse

|

Contract,Perm Possible

|

$40 - $50 (hourly estimate)

{"JobID":381044,"JobType":["Contract,Perm Possible"],"EmployerID":null,"Location":{"Latitude":-75.1569090909091,"Longitude":39.9500909090909,"Distance":null},"State":"Pennsylvania","Zip":"19140","ReferenceID":"HPA-733518","PostedDate":"\/Date(1726496059000)\/","Description":"Our client is looking for a clinical research nurse to join their school of medicine team to assist in all research studies for pulmonary diseases. This person will be working between handling clinical visits for inpatient and outpatient trials and then data entry and administrative work. Majority of the role will be handling EKGs and drawing blood from patient volunteers. The position will work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual, and coordinate the timely study activation and submission of protocol amendments. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Clinical Research Nurse","City":"Philadelphia","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- PA RN License or compact license - 3+ years experience as a registered nurse (if no clinical research background) - Registered Nurse in Clinical Research, Pulmonology, or ICU - BLS/ CPR cert","Skills":"Experience with pulmonary clinical trials CCRP (Cert Clin Research Prof) certification","Industry":"Nurse","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":50.0000,"SalaryLow":40.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Our client is looking for a clinical research nurse to join their school of medicine team to assist in all research studies for pulmonary diseases. This person will be working between handling... clinical visits for inpatient and outpatient trials and then data entry and administrative work. Majority of the role will be handling EKGs and drawing blood from patient volunteers. The position will work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual, and coordinate the timely study activation and submission of protocol amendments. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Oct 03, 2024

Skokie, IL

|

Nurse

|

Contract-to-perm

|

$30 - $38 (hourly estimate)

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Insight Global is looking for a clinical denials specialist to join the team at one of your healthcare clients in Chicago. As a Clinical Denials Specialist you will be working with the denials team... to review and analyze denials from a clinical perspective. This person will be responsible for preparing appeals and communication with the clinical team members. With a strong focus on maximizing patient outcomes and optimizing resource allocation, this position requires exceptional clinical knowledge, excellent communication skills, and the ability to thrive in a fast-paced and ever-changing healthcare environment.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Oct 03, 2024

Irvine, CA

|

Administrative Assistant

|

Contract

|

$51 - $64 (hourly estimate)

{"JobID":384455,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-117.706636363636,"Longitude":33.6702727272727,"Distance":null},"State":"California","Zip":"92618","ReferenceID":"OCC-738778","PostedDate":"\/Date(1727954035000)\/","Description":"A medical device company located in Irvine, CA is looking for a Sr. Clinical Research Specialist to play a critical role in the design, execution, and management of clinical research studies. The responsibilities include but are not limited to: Study Design and Planning: Develop and design clinical research protocols, ensuring alignment with regulatory requirements and company objectives. Project Management: Oversee the execution of clinical trials, including site selection, patient recruitment, data collection, and monitoring. Regulatory Compliance: Ensure all clinical research activities comply with FDA regulations, ICH-GCP guidelines, and other relevant regulatory standards. Data Analysis and Reporting: Analyze clinical trial data and prepare comprehensive reports for internal and external stakeholders. Vendor Management: Manage relationships with clinical sites and other external partners to ensure high-quality and timely execution of clinical studies. Risk Management: Identify and mitigate potential risks associated with clinical trials to ensure patient safety and data integrity.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Sr. Clinical Research Specialist","City":"Irvine","ExpirationDate":null,"PriorityOrder":0,"Requirements":"7+ years of experience in clinical research focused on medical device or pharmaceuticalExperience with site managementExperience with EDC and ETMFProject management experience - finances, accruals, invoices from vendorsBachelor\u0027s Degree","Skills":"","Industry":"Administrative Assistant","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":64.0000,"SalaryLow":51.2000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A medical device company located in Irvine, CA is looking for a Sr. Clinical Research Specialist to play a critical role in the design, execution, and management of clinical research studies. The... responsibilities include but are not limited to: Study Design and Planning: Develop and design clinical research protocols, ensuring alignment with regulatory requirements and company objectives. Project Management: Oversee the execution of clinical trials, including site selection, patient recruitment, data collection, and monitoring. Regulatory Compliance: Ensure all clinical research activities comply with FDA regulations, ICH-GCP guidelines, and other relevant regulatory standards. Data Analysis and Reporting: Analyze clinical trial data and prepare comprehensive reports for internal and external stakeholders. Vendor Management: Manage relationships with clinical sites and other external partners to ensure high-quality and timely execution of clinical studies. Risk Management: Identify and mitigate potential risks associated with clinical trials to ensure patient safety and data integrity.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Oct 09, 2024

Franklin Lakes, NJ

|

Project Manager

|

Contract,Perm Possible

|

$40 - $50 (hourly estimate)

{"JobID":385391,"JobType":["Contract,Perm Possible"],"EmployerID":null,"Location":{"Latitude":-74.1972818181818,"Longitude":41.0266454545455,"Distance":null},"State":"New Jersey","Zip":"07417","ReferenceID":"NNJ-739860","PostedDate":"\/Date(1728461644000)\/","Description":"Insight Global is looking for a Clinical Project Leader to support one of our large Medical Device clients in Franklin Lakes, NJ. This person will be responsible for designing studies, formulating and conducting scientific investigations, feasibility studies, and due diligence studies related to new technologies and current products. They will be expected to interpret/present results, prepare technical reports, journal submissions, and present at scientific meetings. This position interacts cross-functionally with the Quality, Regulatory, Marketing, and Manufacturing functions of the organization. They will review information and assess risks related to vendor, material, and manufacturing process changes. The main goal of this position is to represent Medical Affairs in areas that involve innovation, technology development, product development, and product lifecycle management teams.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Clinical Project Coordinator","City":"Franklin Lakes","ExpirationDate":null,"PriorityOrder":0,"Requirements":"2+ years of experience in clinical study research and study designExperience designing and interpreting results of investigations, feasibility testing, and clinical studiesAbility to understand, interpret and explain clinical and scientific informationExperience in Medical Device industryBachelor\u0027s Degree in Chemistry or related scientific field","Skills":"Masters in Scientific or related field","Industry":"Project Manager","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":50.0000,"SalaryLow":40.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is looking for a Clinical Project Leader to support one of our large Medical Device clients in Franklin Lakes, NJ. This person will be responsible for designing studies, formulating... and conducting scientific investigations, feasibility studies, and due diligence studies related to new technologies and current products. They will be expected to interpret/present results, prepare technical reports, journal submissions, and present at scientific meetings. This position interacts cross-functionally with the Quality, Regulatory, Marketing, and Manufacturing functions of the organization. They will review information and assess risks related to vendor, material, and manufacturing process changes. The main goal of this position is to represent Medical Affairs in areas that involve innovation, technology development, product development, and product lifecycle management teams.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Sep 27, 2024

Fayetteville, AR

|

Computer Operator

|

Contract

|

$51 - $64 (hourly estimate)

{"JobID":383358,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-94.1454545454546,"Longitude":36.0802727272727,"Distance":null},"State":"Arkansas","Zip":"72703","ReferenceID":"BEN-737420","PostedDate":"\/Date(1727421421000)\/","Description":"A local healthcare organization is seeking 11 skilled and detail-oriented Epic Systems Analysts to join their IT team. This team will be responsible for the implementation, support, and optimization of Epic Systems applications. This role requires a deep understanding of clinical workflows, system configuration, and data analysis to ensure the effective use of Epic Systems in improving patient care and operational efficiency.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Epic Analyst - Clinical Documentation","City":"Fayetteville","ExpirationDate":null,"PriorityOrder":0,"Requirements":"***Must be Epic certified in Clinical Documentation (prefers some type of inpatient rehab certification)*** Epic Systems certification in one or more modules (e.g., EpicCare Ambulatory, EpicCare Inpatient, etc.) Minimum of 6 months experience working with Epic Systems in a healthcare setting Strong understanding of clinical workflows and healthcare operations Excellent problem-solving and analytical skills Strong communication and interpersonal skills Ability to work independently and as part of a team","Skills":"Experience with Epic Systems implementation projects. Knowledge of healthcare regulations and compliance standards.- Project management experience.- Bachelors degree in Information Technology, Healthcare Administration, or a related field","Industry":"Computer Operator","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":64.0000,"SalaryLow":51.2000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A local healthcare organization is seeking 11 skilled and detail-oriented Epic Systems Analysts to join their IT team. This team will be responsible for the implementation, support, and optimization... of Epic Systems applications. This role requires a deep understanding of clinical workflows, system configuration, and data analysis to ensure the effective use of Epic Systems in improving patient care and operational efficiency.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Sep 17, 2024

Franklin, TN

|

QA

|

Contract-to-perm

|

$46 - $58 (hourly estimate)

{"JobID":381308,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-86.8227272727273,"Longitude":35.9279090909091,"Distance":null},"State":"Tennessee","Zip":"37067","ReferenceID":"HTN-734713","PostedDate":"\/Date(1726578865000)\/","Description":"We are looking for a local manual QA engineer who specializes in EMR testing. The QA team plays a crucial role in ensuring the accuracy and reliability of EMR configuration changes. Once the configuration team makes changes, QA reviews and runs end to end, functional and regression tests to identify any issues or bugs. They validate the changes in a controlled environment before the updates are moved to production.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Clinical QA Tester","City":"Franklin","ExpirationDate":null,"PriorityOrder":0,"Requirements":"5+ years of manual testing within the EMR space EMR/EHR Deployment and Integration ExperienceADO or JIRA experience","Skills":"Change Management Experience Design, develop, and execute automation scripts using open-source toolsBehavioral healthcare","Industry":"QA","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":58.0000,"SalaryLow":46.4000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

We are looking for a local manual QA engineer who specializes in EMR testing. The QA team plays a crucial role in ensuring the accuracy and reliability of EMR configuration changes. Once the... configuration team makes changes, QA reviews and runs end to end, functional and regression tests to identify any issues or bugs. They validate the changes in a controlled environment before the updates are moved to production.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Sep 04, 2024

Orange, CA

|

EMR Electronic Medical Records

|

Contract-to-perm

|

$56 - $70 (hourly estimate)

{"JobID":378532,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-117.857181818182,"Longitude":33.7834545454545,"Distance":null},"State":"California","Zip":"92868","ReferenceID":"HSW-730974","PostedDate":"\/Date(1725452045000)\/","Description":"As a technical leader in clinical applications, applies advanced professional concepts and extensive industry knowledge to lead and / or work on medium to large projects of broad scope and complexity. The incumbent provides support for all computer and information systems activities of the Pathology Department. Monitors activity and maintains LIS performance and integrity to ensure highest standards of patient care and compliance with all applicable regulations. Incumbent may be required to chair user group and validation committees with technical specialists and physicians across the Health System. Collaboration: Work with lab leaders, other analysts, section heads, and SMEs to gather preliminary information for builds. Build and Testing: Perform builds, testing, and keep tabs on lab items. Support: Provide ongoing support for Beaker and third-party systems, including rotational on-call duties towards the end of go-live.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Clinical Applications Professional IV - Beaker","City":"Orange","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Experience: 3-5 years of experience as a Clinical Application Professional - Beaker Certifications: Beaker CP certification \u0026 CLS/MedTech in California. Skills: Proficiency in Beaker CP. Education: Bachelor\u0027s degree in health care information technology, computer science, or related area, and or equivalent combination of experience/training.","Skills":"Additional Experience: DI experience, HL7 interface experience, Lifepoint experience, and Beaker AP knowledge. Implementation: Prior direct experience with implementations. Knowledge of LIS maintenance, including new test builds Certifications: Epic Beaker Certification, Current California Clinical Lab Scientist or Cytotechnologist License Billing: Experience with EPIC billing.","Industry":"EMR Electronic Medical Records","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":70.0000,"SalaryLow":56.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

As a technical leader in clinical applications, applies advanced professional concepts and extensive industry knowledge to lead and / or work on medium to large projects of broad scope and... complexity. The incumbent provides support for all computer and information systems activities of the Pathology Department. Monitors activity and maintains LIS performance and integrity to ensure highest standards of patient care and compliance with all applicable regulations. Incumbent may be required to chair user group and validation committees with technical specialists and physicians across the Health System. Collaboration: Work with lab leaders, other analysts, section heads, and SMEs to gather preliminary information for builds. Build and Testing: Perform builds, testing, and keep tabs on lab items. Support: Provide ongoing support for Beaker and third-party systems, including rotational on-call duties towards the end of go-live.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Sep 16, 2024

Baltimore, MD

|

Social Worker

|

Perm

|

$86k - $90k (estimate)

{"JobID":381018,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-76.5870909090909,"Longitude":39.321,"Distance":null},"State":"Maryland","Zip":"21230","ReferenceID":"BAL-731486","PostedDate":"\/Date(1726488950000)\/","Description":"- Licensed Clinical Supervisor will service the SE region with one other supervisor- Able to sit states including: VA, NC, SC, TN, GA, KY, AL- Will service and travel to states including: VA, NC, SC, TN, GA, KY, AL, possibly outside the region in emergent circumstances - Reporting to the Associate Director for Clinical Oversight, the PRS Intervention Supervisor will provide clinical supervision to intensive case management staff. - The Licenses Clinical (PRS Intervention) Supervisor will ensure quality service provision and coordination of services to unaccompanied children (UC) released from federal custody. - They will ensure clinical oversight and support to staff (PRS Intervention Case Managers - Level 3) to ensure the implementation of high-quality intensive intervention case management services- 5-6 PRS Intervention Case Managers (level 3) will be their direct reports - Manage small case load of 1-2 PRS intervention cases - Willing and able to clear a criminal background check for the past 7 years. - Willing and able to request and clear Child Abuse and Neglect background check in all states lived within previous 5 years, updated as required.- Obtain a negative TB Test yearly.- Willing and able to obtain FBI fingerprint check every 5 years.- Must have valid driver\u0027s license and MVA check free of major infractions for the last 7 years. - Ability to travel to home visits and other service agencies to serve the client, either by own vehicle or by public transportation (train, plane, etc.).- Availability of a vehicle that meeting safety and mechanical requirements for travel within an assigned radius.- Up to 50% travel required.Compensation:$86,250 to $90,000 per year annual salary. Exact compensation may vary based on several factors, including skills, experience, and education.Benefit packages for this role include: Medical, dental, vision available the first day of employment, Professional development, tuition reimbursement, Generous paid time off including 20 days of vacation, 12 days of sick leave, 12 paid holidays, 12 weeks of fully paid parental leave and up to 12 weeks of fully paid FMLA leave, Company 403(b) contribution of 3%, an additional 7% match which vests immediately, Family Building benefits for reproductive procedures, adoption/foster care assistance An annual wellness benefit of $1,500 that can be customized to support your personal needs including funding enrichment classes, gym memberships, and healthy eating plans (to name a few) all in an inclusive and progressive environment!We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Licensed Clinical Supervisor - SE Region","City":"Baltimore","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- Master\u0027s degree in social work, psychology or other relevant behavioral science in which clinical experience is a program requirement, plus at least five years of postgraduate direct service experience.- At least three years of experience providing administrative supervision and clinical supervision to case managers.- Experience working with diverse client populations, particularly immigrants and refugees - Licensed to provide clinical supervision.- Strong analytical and problem-solving skills.- Bi-lingual English and Spanish","Skills":"","Industry":"Social Worker","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":90000.0000,"SalaryLow":86250.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

- Licensed Clinical Supervisor will service the SE region with one other supervisor- Able to sit states including: VA, NC, SC, TN, GA, KY, AL- Will service and travel to states including: VA, NC, SC,... TN, GA, KY, AL, possibly outside the region in emergent circumstances - Reporting to the Associate Director for Clinical Oversight, the PRS Intervention Supervisor will provide clinical supervision to intensive case management staff. - The Licenses Clinical (PRS Intervention) Supervisor will ensure quality service provision and coordination of services to unaccompanied children (UC) released from federal custody. - They will ensure clinical oversight and support to staff (PRS Intervention Case Managers - Level 3) to ensure the implementation of high-quality intensive intervention case management services- 5-6 PRS Intervention Case Managers (level 3) will be their direct reports - Manage small case load of 1-2 PRS intervention cases - Willing and able to clear a criminal background check for the past 7 years. - Willing and able to request and clear Child Abuse and Neglect background check in all states lived within previous 5 years, updated as required.- Obtain a negative TB Test yearly.- Willing and able to obtain FBI fingerprint check every 5 years.- Must have valid driver's license and MVA check free of major infractions for the last 7 years. - Ability to travel to home visits and other service agencies to serve the client, either by own vehicle or by public transportation (train, plane, etc.).- Availability of a vehicle that meeting safety and mechanical requirements for travel within an assigned radius.- Up to 50% travel required.Compensation:$86,250 to $90,000 per year annual salary. Exact compensation may vary based on several factors, including skills, experience, and education.Benefit packages for this role include: Medical, dental, vision available the first day of employment, Professional development, tuition reimbursement, Generous paid time off including 20 days of vacation, 12 days of sick leave, 12 paid holidays, 12 weeks of fully paid parental leave and up to 12 weeks of fully paid FMLA leave, Company 403(b) contribution of 3%, an additional 7% match which vests immediately, Family Building benefits for reproductive procedures, adoption/foster care assistance An annual wellness benefit of $1,500 that can be customized to support your personal needs including funding enrichment classes, gym memberships, and healthy eating plans (to name a few) all in an inclusive and progressive environment!We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Oct 01, 2024

Philadelphia, PA

|

Nurse

|

Contract-to-perm

|

$39 - $49 (hourly estimate)

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The Clinical Research Nurse performs basic nursing skills, study coordination, and data management for phase 1 early drug development cancer research. Focusing on managing subject recruitment and... enrollment, consistency of study implementation, integrity, and compliance with regulatory requirements and reporting. They are working with sponsors and CROs. The role is Monday-Friday, 8-4:30; however, this candidate will work longer hours as needed. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

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