Clinical Trial Manager I: Site

PSI CRO is seeking a Site Contract Specialist I who can be based anywhere in Canada. The role centers on negotiating site agreements and budgets to support site activation, tailoring agreements for country and site needs, and coordinating the signing process. Responsibilities include tracking negotiations, maintaining Trial Master File records, and keeping...

Clinical Trial Manager – Clinical Operations For over 25 years, dicentra has been a trusted global leader in regulatory consulting and clinical research for the life sciences and dietary supplement industries. We partner with innovators worldwide to navigate complex regulatory landscapes, turn scientific rigor into commercial success, and bring safe,...

dicentra Inc. is seeking an experienced Clinical Trial Manager to oversee active programs, site operations, and monitoring activities. The role can be full-time, part-time fixed-term, or independent consulting, depending on experience. You will own operational delivery for studies across phases, ensure ICH-GCP compliance, and coordinate with data management...

Parexel International is seeking a Senior Clinical Research Associate (Sr. CRA) to manage investigator sites, monitor trial conduct, and oversee close-out to ensure patient safety and data quality in line with GCP and sponsor standards. The role involves active collaboration with the Site Care Partner and study team. The Sr. CRA will lead monitoring...

ICON plc in Canada seeks a detail-oriented Clinical Operations Associate to support budgeting, document management, site administration, and cross-country coordination. You will help prepare budgets, contracts, and study submissions while ensuring compliant processes across CTMS/eTMF systems. You will manage on-site sponsor presence two days a week in...

Manage Canadian clinical trial start-up submissions using Health Canada knowledge and precise regulatory documentation from a remote position. Coordinate approvals and timelines for Premier Research projects. As a Site Start-up Associate II, you support Premier Research’s Clinical Monitoring, Site Management and SSU team. You prepare Central and Local EC...

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical...

Worldwide Clinical Trials is seeking a Project Manager to oversee clinical trials from start-up to close-out. You will lead cross-functional teams, manage resources with functional heads, and ensure deliverables meet time/quality/cost expectations across local, regional, or global scopes.The role requires 5+ years in clinical pharmaceutical project...

Clinical site monitoring expertise drives this remote Clinical Research Associate position at Parexel, supporting study quality, patient protection, and site relationships. As a Clinical Research Associate, you will manage assigned sites from identification through close-out. You will serve as the sites’ sole contact, resolve questions, and oversee...