Job Description
Insight Global is looking for a Senior Clinical Trial Manager to provide strategic and operational leadership to Clinical Trial Managers and associated study staff in support of global clinical programs. This role is accountable for the planning, execution, and oversight of RDN clinical trials, ensuring alignment with program strategy, timelines, budgets, quality standards, and regulatory requirements. The Senior Manager drives clinical excellence across studies, oversees vendor performance, and ensures audit readiness throughout the lifecycle of each trial. This role leads and develops Clinical Trial Managers and assigned study personnel while overseeing the end‑to‑end operational execution of global clinical trials in compliance with protocols, GCP, SOPs, and regulatory requirements. The individual translates program strategy into operational plans, timelines, and resource needs, ensuring cross‑functional alignment and on‑time delivery of study milestones. Responsibilities include oversight of study documentation, systems, and regulatory submissions; management of CROs and external vendors including performance, issue escalation, and budgets; and proactive risk identification and mitigation. The role provides clear, data‑driven updates and recommendations to clinical leadership, maintains financial oversight of clinical trial budgets, builds strong relationships with investigators and clinical sites to support enrollment, ensures inspection readiness, and drives continuous improvement across clinical operations processes and best practices. Pay range: $70-$90
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
• Bachelor’s degree in a scientific or healthcare discipline; advanced degree preferred.
• 10 years of experience in clinical research, including global clinical trials and vendor management.
• 5 years of demonstrated leadership experience managing and developing clinical trial staff, preferred.
• Strong understanding of GCP, ICH guidelines, and global regulatory requirements.
• Proven ability to manage complex timelines, budgets, and cross‑functional deliverables.
• Excellent communication, negotiation, and stakeholder‑management skills.
• Ability to navigate ambiguity, drive decision‑making, and influence across levels of the organization.
• Proven exposure and experience to internal audits and regulatory body audits
• Ability to work in fast-paced environment requiring support of multiple studies and direct reports simultaneously
Nice to Have Skills & Experience
Renal denervation experience
Clinical trial management experience
People management of clinical trials
Clinical Trial execution experience
Cardiology Clinical trials experience
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.