Parexel

Lead global site contract negotiations as an Investigator Contracts Lead in Australia. This FSP role requires expertise in drafting and negotiating Clinical Trial Agreements (CTAs) and managing study-level budgets. Leverage your 5+ years in clinical development or a Juris Doctorate to mitigate ri...

Join Parexel Consulting as a **Regulatory Affairs Associate** specializing in **Annual Reports & Renewals for Biologics**. Leverage your 2-4 years of **Regulatory Affairs-CMC** experience to support global submissions (US/EU/Brazil/LATAM/China). Work remotely from India, collaborating with cross-...

Lead RWD Strategy as Director at Parexel in Spain, driving healthcare innovation through real-world data. Leverage 10+ years of CRO/Pharma experience and expertise in patient data models (OMOP, CDISC) to shape bid proposals and vendor management. This role offers the chance to integrate cutting-e...

Seeking a Clinical Laboratory Study Manager in the US to drive precision medicine strategies. Requires 6+ years of clinical research experience, a life sciences degree, and expertise in GCP/ICH guidelines. You will manage sample logistics, develop study documents, and collaborate with cross-funct...

Join Parexel as a Clinical Research Associate II in Milan, Italy. Leverage your 2+ years of independent monitoring and site management experience to ensure patient safety and data integrity. Build strong investigator relationships while managing global, multi-sponsor clinical trials across divers...

Parexel seeks a Trial Vendor Senior Manager in the UK, Ireland, or France to independently oversee all vendor aspects of global clinical trials. This role requires 3+ years of experience with GxP/ICH regulations, eCOA, IRT, and Central Labs. You will manage vendor risks, budgets, and performance ...

Seeking a **Site Contracts Lead** for a **FSP** role in **Canada**. You will lead direct, site-facing contract and budget negotiations for clinical investigator sites, managing the full lifecycle from initial agreements to amendments. Leverage your expertise in **Clinical Trial Agreements** and *...

Senior Regulatory Affairs Associate (CMC Biologics/Vaccines) role at Parexel Consulting. Leverage your CMC and post-approval expertise to develop regulatory strategies for biopharma clients. Enjoy remote work from Serbia while managing submissions, change controls, and health authority interactio...

Lead cross-functional teams as a **Manager, Project Planner** at Parexel in Canada. Drive high-quality clinical trials by managing project schedules, budgets, and resources. Requires 3+ years in pharmaceutical project planning and a Bachelor’s degree. Enjoy a supportive environment with flexible ...

Seeking an experienced **Study Start Up Project Manager** for a remote FSP role in Canada. You will define and deliver global start-up strategies for interventional studies across oncology, vaccines, and rare disease. Requires extensive global clinical trial management, GCP expertise, and fluency...

Seeking a Country Study Operations Manager / Clinical Trial Manager for a FSP role in Canada. Lead local study teams, manage CROs, and oversee country-level activities from startup to closeout. Requires a Bachelor’s degree with 5+ years or a Master’s with 3+ years of operational clinical trial ex...

Associate Director, Solution Enablement (System Owner) role in Canada, driving business value through technology. You will act as the key liaison for critical business solutions, maximizing ROI and improving service for patients and sponsors. Requires strong collaboration, strategic thinking, and...