Parexel - Remote work

Parexel FSP seeks a Senior Analyst, Site Contracts & Budgets in Argentina to manage end-to-end clinical site agreements and budgets. You will negotiate CTAs, ensure FMV compliance, and collaborate with cross-functional teams. Ideal candidates bring 3-5 years of pharma/biotech contract experience ...

We are seeking a Country Clinical Trial Manager / Local Trial Manager for a future opening in Italy. This fully remote, home-based role requires 5+ years of end-to-end clinical trial management experience and expertise in patient document localization. You will lead study start-up, site activatio...

Seeking a Principal Medical Writer, Patient Safety for a remote role based in Bengaluru, India. You will independently lead complex aggregate safety reports, serving as a subject matter expert on regulatory submissions. Requires strong analytical skills, exceptional medical writing, and client-fo...

Parexel FSP seeks a Trial Vendor Senior Manager in Poland to lead global vendor operations for early-phase clinical trials. You will manage IRT, eCOA, central labs, and budgets, ensuring quality and compliance. Ideal candidates have 7+ years of vendor management experience and a global study team...

Senior Clinical Research Associate (Oncology) sought by Parexel in the UK. Leverage 5+ years of CRO/pharma experience and essential oncology/RECIST expertise to ensure patient safety and data integrity. This role involves global monitoring, regulatory compliance, and building strong site relation...

Senior Medical Writer, Patient Safety role in Bengaluru, India. Lead the preparation of complex aggregate safety reports (PSURs, PBRERs, DSURs) and drive strategic safety submissions. Requires expertise in pharmacovigilance regulations and signal detection. Join a team focused on global complianc...

Senior Regulatory Affairs Associate sought to lead clinical trial submissions in Peru and LATAM via the REPEC Platform. Leverage 5+ years of regulatory expertise to act as Local Regulatory Contact and Global Regulatory Lead, preparing dossiers and labels. This remote role offers strategic client ...

Senior Clinical Data Analyst sought by Parexel for remote roles in the UK, Poland, or South Africa. Leverage 5-8 years of pharmaceutical data management expertise and Phase I experience to lead global studies. Drive eCRF design, vendor oversight, and regulatory compliance (ICH/FDA, CDISC). Enjoy ...

Senior Director, Events role at Parexel, based in the United States. Lead global event strategy, drive lead generation, and enhance brand engagement. Requires 15+ years of meeting planning experience, 5+ years in team leadership, and expertise in executive communications. Oversee high-impact conf...

Join Parexel Consulting as a Regulatory Affairs Consultant specializing in CMC for vaccines/bio. Leverage your expertise in CMC, post-approval requirements, and biological processes to develop submission strategies for clients. This UK-based role offers flexible work arrangements, requiring stron...

Senior Regulatory Affairs Associate sought for Parexel Consulting to lead radiopharmaceutical lifecycle management. Leverage expertise in CMC authoring, safety labelling, and Health Authority submissions. This remote role based in India offers flexible work, global client exposure, and mentorship...

Seeking an experienced **Director RWD Strategy** to join Parexel in the **United Kingdom**. Leverage 10+ years of CRO/Pharma expertise to lead **proposal development** and drive **real-world data** acquisition across Europe. Requires a Master’s in life sciences or data science, deep knowledge of ...