Parexel

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 ...

Join Parexel as a Project Specialist in Mexico, leading cross-functional teams to deliver patient-focused clinical trials. You’ll manage project timelines, budgets, and reporting, requiring strong MS Excel skills and business-level English. Benefit from a supportive, inclusive environment with hi...

Vice President, Project Leadership role driving strategic oversight for clinical trial delivery across the US. Seeking expert project management experience in healthcare or CROs, with proven global matrix leadership. You will lead Directors, ensure financial and quality targets, and foster authen...

Associate Manager, Clinical Operations in Bengaluru, India. Oversee clinical trial teams, ensuring high-quality, on-time project delivery. Requires substantial monitoring or data management experience and a degree in a health-related field. Drive team performance, resource planning, and client pr...

Join Parexel as a Statistical Programmer II in Taipei, Taiwan. Leverage your SAS expertise and analytical skills to analyze clinical trial data, ensuring safety and efficacy. Collaborate on global projects, producing SDTM/ADaM datasets and regulatory submissions in a quality-focused environment. ...

Seeking a Principal Physician, Patient Safety in India to lead drug safety expertise. This role requires clinical medicine experience and deep knowledge of drug development and global safety regulations. You will manage adverse event profiles, act as a Subject Matter Expert, and collaborate with ...

Join Parexel as a **Project Specialist** in Taipei, Taiwan, and lead cross-functional teams to deliver patient-focused clinical trials. This role demands strong communication skills, attention to detail, and a client-focused approach to manage timelines and budgets. Enjoy a supportive environment...