Parexel

Seeking a Clinical Research Associate II in Taipei, Taiwan to join Parexel’s global team. You will ensure patient safety and study integrity by monitoring investigator sites, building strong relationships, and resolving issues. Ideal candidates have site management experience, a degree in a healt...

HR Associate role in Bucharest, Romania, serving as the first point of contact for HR support. Requires fluency in English, strong communication skills, and a Bachelor’s in HR or related field. Responsibilities include managing employee inquiries, leading cross-functional projects, and ensuring d...

Lead global, patient-focused clinical trials as a **Global Clinical Trial Leader** with Parexel. This home-based role in the UK requires 5+ years of **clinical trial management** experience, expertise in **Oncology, CNS, Immunology, or Vaccines**, and strong leadership skills. You will manage cro...

Lead early-phase clinical trials as a **Project Manager** at Parexel, driving cross-functional teams to deliver life-changing treatments. This remote role requires 2+ years of PM experience (or 3-5 in related fields), ICH-GCP knowledge, and strong leadership. You will own sponsor relationships, m...

MLR Vault Technician role in India seeks a detail-oriented professional to manage content within Veeva Vault PromoMats and Medical. Key duties include creating placeholders, uploading versions, and reference linking in a cross-functional environment. Ideal candidates have a scientific background ...

Join Parexel Consulting as a Health Economics Consultant (Evidence Evaluation) in Remote India. Leverage your HEOR and SLR expertise to deliver high-quality, strategic solutions for biopharma clients. Requires a Master’s/PhD in Life Sciences, 5+ years in evidence evaluation, and strong analytical...

Join Parexel as a Site Visit Report Reviewer (SVRR) in India. You will ensure clinical visit reports meet GCP, SOP, and regulatory standards while collaborating with CRAs and project teams. Monitor open issues, protocol deviations, and SAEs to closure. Ideal for detail-oriented professionals with...

Join a global FSP team as a GCO Associate I in the UK. Leverage your 2-5 years of clinical trial support or site activation experience to execute start-up, conduct, and close-out tasks. You will maintain trackers, support documentation workflows, and coordinate with vendors. Ideal for life scienc...

Join Parexel as a Patient Safety Associate I in the United States. Leverage your 3+ years of Drug Safety experience to process ICSRs, conduct literature reviews, and support signal detection in post-market surveillance. Ideal candidates have expertise in cardiology, oncology, or rare disease, plu...

Join Parexel Consulting as a Health Economics Associate in India, focusing on modelling to evaluate cost-effectiveness for global reimbursement. Leverage your expertise in VBA, SAS, or R, along with a Master’s in health economics or a quantitative field. Enjoy remote flexibility, diverse client e...

Senior Physician, Patient Safety role in India seeks an MBBS/MD with 2+ years of ICSR medical review experience. You will ensure global drug safety compliance, manage adverse event reporting, and serve as a Subject Matter Expert. Ideal for pharmacovigilance professionals with strong medical termi...