Parexel

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...

Clinical Finance Analyst II responsible for processing investigator and vendor invoices, reconciling payments, and supporting clinical trial financials. Requires 4+ years of AP/AR experience in biotech or finance. Key duties include database maintenance, audit trail support, and cross-functional ...

Seeking a Scientist III for a long-term FSP role in Rahway, NJ, specializing in LC-MS and Analytical Support. This lab-based position requires a BS/MS in Chemistry with 3-5 years of experience operating Waters, Sciex, or Agilent LC-MS systems. Key duties include maintaining open access instrument...

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...

Seeking a Scientist III – Potency Assay for a long-term FSP assignment in Rahway, NJ. This lab-based role requires a Bachelor’s or Master’s in Biology/Molecular Biology with industry experience in sterile cell culture and aseptic technique. Execute cell-based potency assays, maintain cell lines, ...

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...

Seeking a **Central Monitor II** in **Romania** to drive clinical trial oversight. You will implement centralized monitoring strategies, analyze data for trends, and identify risks using KRIs and QTLs. Requires a life science degree, 5+ years pharma experience, and strong clinical monitoring expe...

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...

Parexel seeks a Site Contract Associate II to join its Site Contracts team, supporting the DACH region remotely from Serbia or Romania. This role requires fluent German and English, focusing on negotiating, finalizing, and executing clinical study agreements and amendments. Ideal candidates posse...

Senior Manager, Third Party Quality Lead (FSP) sought in Brazil. Leverage 7+ years of pharma experience to oversee GCP quality risk management for clinical trial vendors. Drive compliance, audits, and CAPA processes while fostering a culture of quality. Lead global quality discussions and ensure ...

Senior Clinical Research Associate sought in Israel for a dedicated client role. Leverage 5+ years of oncology and site management expertise to oversee all monitoring visits. Join Parexel to mentor junior CRAs, work with world-class technology, and drive global drug development. Enjoy a premium s...