Parexel - IT - Administration

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 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...

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...

Lead global clinical trials in dermatology as a Project Leadership expert at Parexel. Drive cross-functional teams to deliver patient-focused studies on time and within budget. Requires 2+ years of CRO/biotech PM experience, a clinical degree, and strong leadership skills. Join a mission to accel...

Senior Manager, Patient Safety – Hyderabad, India. Lead end-to-end medical device complaint handling and post-market surveillance, ensuring full compliance with FDA 21 CFR 803/820 and global regulations. Drive operational excellence, mentor high-performing teams, and partner with Quality, Regulat...

Senior Regulatory Affairs Associate sought for remote role based in Bloemfontein, South Africa. You will manage Clinical Trial Applications (CTA) and lead regulatory submissions across Southern Africa. Ideal candidates possess a science degree, CTA experience in South Africa, and expertise in Vee...

Parexel FSP seeks an Investigator Contracts Lead I for a 100% remote, sponsor-dedicated role in Spain. You will lead site-facing contract and budget negotiations for clinical trial agreements, leveraging 3+ years of experience in clinical development. This position offers a premium salary, attrac...

Join Parexel FSP as a Global Site Start-Up Lead, home-based in Spain, Poland, Serbia, or Romania. Drive global site activation for sponsor-dedicated clinical trials, leveraging 4-6 years of SSU and regulatory expertise. Enjoy a premium salary, comprehensive benefits, and a collaborative culture w...

Join Parexel as a Regulatory Affairs Consultant (Labelling) for a remote role in Switzerland. Leverage your German fluency and CCDS expertise to manage global labelling lifecycles for biopharma clients. Drive regulatory strategies, ensure Swissmedic compliance, and support harmonization in a coll...

Parexel seeks a Workday Change Management Specialist to drive global HCM adoption. You will develop communications and training materials for diverse audiences, leveraging AI tools and SharePoint. Ideal candidates have 2-3 years of change management experience and Workday HCM knowledge. This UK-b...

Join Parexel as an Initiation Clinical Research Associate in Brazil. We seek a detail-oriented, self-starter with strong problem-solving skills to manage site start-up activities, including CDA negotiation and TMF management. This role offers flexible work arrangements and requires excellent comm...

Join Parexel in Buenos Aires as a Desktop Support Technician. Provide first-level IT support, configure laptops, and deploy workstations in a clinical research environment. Requires 1-2 years of experience, Windows/macOS proficiency, and advanced English. Grow your career with a global leader adv...