Parexel

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...

Senior Health Economics Modelling Consultant sought by Parexel Consulting to lead cost-effectiveness and budget impact model development for biopharma clients. Requires 8+ years’ experience in health economics modelling (Excel/VBA, R) and project leadership. Remote UK-based role offers exposure t...