Parexel - IT - Administration, Remote work

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...

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...

Parexel FSP seeks a Senior Analyst, Site Contracts & Budgets in Argentina to manage end-to-end clinical site agreements and budgets. You will negotiate CTAs, ensure FMV compliance, and collaborate with cross-functional teams. Ideal candidates bring 3-5 years of pharma/biotech contract experience ...

We are seeking a Country Clinical Trial Manager / Local Trial Manager for a future opening in Italy. This fully remote, home-based role requires 5+ years of end-to-end clinical trial management experience and expertise in patient document localization. You will lead study start-up, site activatio...

Parexel FSP seeks a Trial Vendor Senior Manager in Poland to lead global vendor operations for early-phase clinical trials. You will manage IRT, eCOA, central labs, and budgets, ensuring quality and compliance. Ideal candidates have 7+ years of vendor management experience and a global study team...