Senior Clinical Study Manager

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Dexcom

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1999

⚕️ Healthcare Insurance

🧬 Biotechnology

Healthcare Insurance • Biotechnology • Wearable Technology

Dexcom is a leading provider of continuous glucose monitoring (CGM) systems, revolutionizing how people manage diabetes and track their glucose levels. Known for their best-in-class glucose biosensing technology, Dexcom offers products like the Dexcom G7 CGM system, which provides real-time glucose monitoring and insights to help individuals become healthier. Founded in 1999, Dexcom has consistently innovated in the field of diabetes management, empowering users to take control of their health with accurate and advanced glucose monitoring solutions. Their products are designed for both adults and children and do not require a prescription.

📋 Description

• Lead cross-functional trial teams (Site Management, Monitoring, Data Management, Biostats, Safety, Clinical Logistics) • Drive country and site feasibility across Europe and select sites based on clinical trial design requirements • Author, review, and approve clinical study protocols and informed consent forms to ensure scientific integrity, regulatory compliance, and ethical standards • Ensure protocol adherence, timely data entry, query resolution, and deviation management • Coordinate with ethic committees and competent authority as needed • Maintain inspection-ready documentation, drive continuous improvement and lessons learned • Serve as the central point of contact for internal/external stakeholders • Prepare updates, risk summaries, and decision briefs to senior leadership • Develop timeline plans and proactively manage path to meet trial milestones (e.g. FPI) • Provide robust vendor oversight (e.g. CROs), escalate and remediate as needed • Lead and drive strategic initiatives, coordinating cross‑functional teams to ensure timely and high‑quality execution

🎯 Requirements

• Experience in leading a clinical trial in all phases (e.g. start up, execution and close out) • Experience in medical devices and/or diabetes clinical trials • Proficient at utilizing clinical management systems and electronic data capture systems • Prior inspection/audit participation • Familiar with post market clinical follow-up, registries, real-world evidence, or adaptive designs • Detailed oriented, strategic thinking, problem solver, and drive decision making • Excellent communication both verbal and written

🏖️ Benefits

• A full and comprehensive benefits program • Growth opportunities on a global scale • Access to career development through in-house learning programs and/or qualified tuition reimbursement • An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve