<Back to Search
Remote Clinical Trial Manager: Lead End-to-End Trials
RemoteApril 1st, 2026
A global leader in engineering and sciences services is looking for a Clinical Trial Manager based in Boston. This role involves overseeing the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards. Candidates should have a Bachelor's degree and at least 6 years in a related role. The position starts fully remote, transitioning to hybrid. Competitive salary offered between $115,000 and $140,000, with additional benefits including a bonus and healthcare options.#J-18808-Ljbffr
Showing all 54,941 matching similar jobs
- Regulatory Compliance Manager
- Senior Counsel, Regulatory
- Associate Clinical Project Manager
- Clinical Project Manager (Hybrid - Acton, MA)
- Associate Director, Project Management (Clinical)
- Sr Regulatory Compliance Specialist
- Senior Counsel - Regulatory
- Director, Clinical Project Management
- Regulatory Affairs Intern
- Sr. Clinical Study Manager - Device
- Head of Regulatory Affairs
- Regulatory Affairs Intern
- Entry-Level Paralegal (Compliance / Regulatory Affairs)
- Clinical Project Manager I (non-MD)
- Sr Clinical Data Project Manager
- Corporate Regulatory Compliance Manager
- Manager, GMG Regulatory - Clinical Regulatory Compliance - Full Time
- Mgr,Clinical Trials Operations
- Clinical Quality Manager - Regulatory & Accreditation - Remote in NC
- Principal Clinical Project Manager Job Details | Olympus Corporation of the Americas
- Associate Clinical Project Manager
- Associate Clinical Project Manager
- Associate Clinical Project Manager
- Sr. Clinical Study Manager - Device
- Manager, Medical Affairs
- Senior Contract Specialist
- Manager, Medical Writing
- Senior Manager, Clinical Operations
- Clinical Project Manager I
- Snr Regulatory Affairs & Compliance Specialist PACE
- Regulatory Specialist, Urology
- Director, Clinical Project Management
- Dietitian
- Metrex Clinical Development Manager (Remote-Brea, CA)
- MDS PPS Coordinator 40 hour
- Sr. Specialist, Regulatory Affairs
- In House Clinical Research Associate
- Senior Medical Writer - Regulatory Documents - CSR /Protocol - Late Phase
- Senior Medical Science Liaison, Metabolic Dysfunction-Associated Steatohepatitis (MASH) Pipeline (Northeast & Midwest)
- Senior Medical Science Liaison, Metabolic Dysfunction-Associated Steatohepatitis (MASH) Pipeline (Northeast & Midwest)