Clinical Project Manager
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About the role
Remote, full-time permanent Clinical Project Manager role based in one of the listed North American locations. The position leads clinical research project planning, execution, monitoring, documentation, budgets, regulatory compliance, patient safety, sponsor communication, and cross-functional delivery. Requires a relevant bachelor's degree, 1–3 years of clinical study management experience, and English fluency. Occasional travel is required.
Key requirements
- • Bachelor's degree in a relevant field, preferably Health Sciences, Clinical Research, or a related discipline.
- • At least 1 year of relevant experience
- • Required skills: clinical study management, clinical research project coordination and execution, clinical research processes, regulatory requirements, quality standards, study documentation practices, project management, organizational skills, cross-functional team coordination, project timeline and deliverable management, budget oversight, patient safety oversight, sponsor and client relationship management, site and patient recruitment support, regulatory submissions, written and verbal communication, problem-solving
- • Required language: English
Opportunity details
- • Workplace: Remote
- • Employment: Permanent
- • Posted: Oct 21, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Clinical Project Manager
Department: Clinical Services
Team: Clinical Study Delivery - Clinical Study Management - Project Management
Location: Raleigh-Durham, North Carolina
All locations: Raleigh-Durham, North Carolina, Philadelphia, Pennsylvania, Cincinatti, Ohio, Houston, Texas, Dallas, Texas, Toronto, Ontario, Vancouver, British Columbia, Montreal, Quebec
Work type: Full-time, Permanent
Workplace type: remote
Salary range: USD 95500 – 159000; per year
Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development.
We operate as a private, profit-with-purpose company, channeling our commercial success back into scientific research, technology, and our people. With approximately 700 people across multiple countries and three service lines, we are growing deliberately, and the capability of our leaders and our organization is central to how we get there.
If you want to do meaningful work, build something real, and invest back in research that changes lives — we want to meet you!
Job Overview
We are seeking a motivated and detail-oriented Clinical Project Manager to oversee the planning, execution, and successful delivery of clinical research projects. In this role, you will coordinate cross-functional teams, manage project timelines and deliverables, ensure regulatory compliance, and maintain strong relationships with sponsors and clients.
The ideal candidate will possess excellent communication, organizational, and problem-solving skills, with a collaborative approach to achieving project objectives. This is a home-based opportunity with occasional travel.
Key Responsibilities
- Lead the planning, execution, monitoring, and completion of assigned clinical research projects, ensuring project objectives and deliverables are achieved.
- Coordinate cross-functional project teams to ensure activities comply with applicable regulations, industry guidelines, corporate policies, and quality standards.
- Oversee project operations, budgets, regulatory requirements, and patient safety to maintain operational and financial integrity throughout the project life cycle.
- Manage the development, maintenance, and appropriate disposal of essential clinical study documents, data, equipment, and tools, including protocols, SOPs, informed consent forms, and case report forms (CRFs).
- Assign, track, and oversee interdisciplinary activities, including site monitoring, database development, data collection, adverse event management, statistical analysis, and clinical study reporting.
Verification
- ✓ Employer verification
- ✓ Original posting located
- Last verified: Oct 23, 2026