Parexel

Lead MAA submissions and regulatory strategy for biopharma clients in this remote project leadership role. Leverage your extensive Regulatory Affairs and CRO experience to manage global filings and ensure client success. Enjoy a flexible work environment with career growth and mentorship from ind...

Join Parexel as a Senior Statistical Programmer to analyze clinical trial data and accelerate new treatments to patients. Utilize your 5+ years of SAS programming and CDISC expertise in a fully remote role across Serbia or Poland. Enjoy a flexible environment with extensive training, career growt...

Lead our Statistical Programming team in Hyderabad, analyzing clinical trial data to accelerate new treatments. You will manage projects and a skilled team across diverse therapeutic areas, ensuring quality deliverables. We offer flexible work, advanced technology, and strong career growth in a s...

Join Parexel as a Senior Clinical Research Associate (CRA) in the United States. You will ensure trial conduct and patient safety, monitoring sites with 60-80% travel. Requires 3+ years monitoring experience, ICH/GCP knowledge, and fluency in English. Work on global projects with career growth in...

Join Parexel's Early Phase Clinical Unit in Baltimore as a Research Associate. Play a crucial role in Phase I trials, conducting participant visits and ensuring protocol compliance. Ideal candidates have clinical experience, a life science background, and phlebotomy skills. This role offers a cle...

Lead IT Operations and Service Desk teams in Hyderabad. Utilize your 6-8 years of IT infrastructure experience and 4-6 years in people management to ensure network uptime and swift issue resolution. Drive continuous improvement, manage escalations, and develop a team of 15 direct reports in this ...

Join Parexel's Biostatistics team in Taiwan to support new treatment efficacy and safety. Utilize your statistical expertise in clinical trials, from protocol input to analysis plans. This role offers project leadership, client interaction, and flexible work arrangements. Experience with SAS and ...

Join Parexel as a Senior CRA II in Turkey. Utilize your 5+ years of monitoring experience, ideally in Oncology, to ensure patient safety and GCP compliance. Manage site operations and enjoy a supportive environment with flexible work arrangements. This FSP role offers global project exposure with...

Join Parexel as a Senior CRA in Istanbul. Drive global clinical trials, ensuring patient safety and ICH-GCP compliance. Enjoy a supportive environment with career growth, flexible work, and diverse therapeutic exposure. Utilize your monitoring expertise and travel to advance treatments.

Join Parexel as a Data Surveillance Analyst. Utilize your clinical data experience and SAS/SQL skills to analyze trends and manage risks in a fully flexible, home-based role. You will develop Data Surveillance Plans and present key findings, ensuring study quality and patient welfare. We offer co...

Join Parexel's Patient Safety team in India as a Japanese-speaking Specialist. You will manage adverse event case processing, safety reporting, and ensure compliance with global regulations. This role requires strong drug safety knowledge, analytical skills, and proficiency in database searches. ...

Join Parexel Consulting as a Regulatory Affairs Consultant specializing in Labelling. Utilize your 8+ years of industry experience to develop global regulatory strategies for biopharmaceutical and medical device clients. This remote role in Australia offers diverse client exposure, career growth,...