Parexel

Seeking a Start Up Project Manager II for a global FSP role in Canada. You will define and deliver complex site activation strategies for interventional studies across diverse therapeutic areas like oncology. Requires proven clinical research, global start-up, and project management experience, w...

Seeking a detail-oriented **HCP Contract Specialist** to manage end-to-end contracting for healthcare professionals and institutions in the **United States**. This role requires strong project management, customer service, and compliance skills, collaborating with legal, finance, and commercial t...

Join Parexel’s Baltimore EPCU as a Per Diem Pharmacy Technician and contribute to life-saving clinical research. This role requires an active Maryland license, 1+ year of experience, and strong attention to detail. Sterile compounding knowledge is highly preferred. Enjoy benefits like PTO, 401k m...

Lead site contracting activities for global clinical trials as an Investigator Contracts Lead in Canada. This role requires expertise in negotiating Clinical Trial Agreements and site budgets with investigators and institutions. Ideal candidates have 5+ years in clinical development operations or...

Seeking a **Regulatory Affairs Consultant** in Bengaluru, India. Leverage 5+ years of experience in pharmaceutical/biotech compliance to manage third-party partner relationships. Ensure regulatory oversight, develop risk mitigation strategies, and monitor partner performance. Enjoy flexible remot...

Join Parexel as a Site Activation Partner in Canada, driving clinical trial success through expert site initiation and activation. Leverage your 2+ years of clinical research experience and ICH/GCP knowledge to manage essential documents and ensure regulatory compliance. This FSP role offers glob...

Senior Clinical Research Associate (Oncology) sought for a remote UK-based FSP role at Parexel. Leverage 4+ years of CRO/pharma experience and RECIST expertise to oversee global oncology trials. Ensure ICH-GCP compliance, build strong investigator relationships, and prioritize patient safety. Enj...

Seeking a Site and Monitoring Health Lead for the Northeast US. This site-facing FSP role ensures GCP compliance and CRO oversight for multinational clinical trials. Requires significant CRO monitoring oversight, Lead CRA experience, and up to 50% travel. Join a team dedicated to inspection-ready...

Seeking a Training Development Lead, Manager in the UK to design global clinical research and pharmacovigilance courses. You need 5+ years in instructional design, adult learning expertise, and skills in Articulate and Adobe. This role offers project management of compliance-driven training for a...

Join Parexel as a Clinical Research Associate I in Bengaluru, India. You will manage site start-up, initiation, and close-out, ensuring patient safety across global projects. Ideal for candidates with substantial start-up experience and a degree in life sciences or nursing. Travel to investigator...

Join a talented team of 40+ as a Meetings Specialist, managing high-quality international pharmaceutical events. We require 3+ years of experience in pharmaceutical event management; Cvent proficiency is a plus. This full-time role offers a competitive salary, annual bonus, and great benefits. Yo...

Seeking a skilled **Workday Integration / Extend Developer** in Bengaluru, India. You will architect, build, and deploy integrations using EIB, Studio, BIRT, and Core Connectors, with a focus on Workday Extend and Orchestrations. Requires 3+ years of hands-on experience, Workday Integration Certi...