Job Description
The Senior Clinical Research Coordinator is responsible for overseeing the day-to-day conduct of research studies while ensuring compliance with sponsor, institutional, and regulatory requirements. This role provides leadership, mentorship, and operational oversight to research staff and supports the successful execution of a diverse portfolio of clinical trials. This role would be responsible for 2-3 direct reports.
Key Responsibilities
• Study Oversight & Operations
• Provide oversight of daily research activities and study conduct across multiple clinical trials.
• Ensure all study procedures are conducted in compliance with sponsor, institutional, federal, and regulatory requirements.
• Support study start-up, maintenance, and close-out activities.
• Monitor study progress and proactively identify and resolve operational issues.
• Team Leadership & Mentorship
○ Mentor, train, and supervise research staff and new team members.
○ Provide guidance on study procedures, policies, and best practices.
○ Foster a collaborative and compliant research environment.
• Process Improvement
○ Develop, implement, and maintain Standard Operating Procedures (SOPs), workflows, and study manuals.
○ Identify opportunities to improve operational efficiency and research quality.
Supporting a broad range of clinical research studies, including:
Pay Range: 45-55/hr
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 HR@insightglobal.com.To 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/.
Required Skills & Experience
• Minimum of 3 years of clinical research coordination experience.
• At least 1 year of Sr level or leadership level experience (serving in a Sr Clinical Research Coordinator or equivalent leadership role)
○ Experience mentoring, training, and supervising research staff and new team members.
• Advanced knowledge of Good Clinical Practice (GCP) guidelines, FDA regulations
• Knowledge of clinical research regulatory requirements and workflows
• Experience with industry sponsored and PI studies (communicating directly with sponsors)
• Experience with Interventional drug trials
Nice to Have Skills & Experience
• Hands on Regulatory experience (local and central IBC submissions)
• Experience working within an academic medical center environment
Experience supporting a broad range of clinical studies
Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.