Parexel

Join Parexel, a leading CRO, as a Clinical Operations Assistant in Brazil. Support Clinical Research Associates with administrative tasks, site payments, and trial master file management. Ideal for healthcare or science graduates with strong English and MS Office skills. Enjoy flexible hours, pro...

Seeking a motivated **LC-MS Scientist** to join our Bioanalytical FSP team in **West Point, PA**. You will validate and utilize LC-MS to support critical drug development sample analysis. Ideal candidates have a Bachelor’s or Master’s in Chemistry/Biochemistry with lab experience and **GLP** fami...

Join us as a Site Care Partner in Mumbai, India, to drive clinical trial success. Leverage your GCP/ICH expertise to manage site start-up, activation, and investigator relationships. We seek strong communicators with cross-functional skills and adaptability to new technologies. Enjoy flexible wor...

Seeking a strategic **Manager, Regulatory Affairs Advertising & Promotion** to join Parexel Consulting remotely in the US. Leverage 7+ years of expertise in FDA regulations to independently review promotional materials and guide cross-functional teams. Act as a trusted SME, shaping regulatory str...

Principal Scientist – Purification Chemist opportunity in Rahway, NJ, with Parexel FSP. Apply chromatography, organic chemistry, and biochemistry expertise to purify APIs and intermediates in an R&D lab. Requires semi-preparative purification experience and strong problem-solving skills. Enjoy fu...

Lead global oncology clinical trials from home as a Project Leadership expert at Parexel. This remote role requires 2+ years managing cross-functional CRO or biotech projects, with expertise in timelines, budgets, and regulatory submissions. Enjoy flexible work arrangements, high accountability, ...

Senior Regulatory Affairs Consultant sought in Seoul, South Korea to lead global project management for biopharma and medical device clients. Leverage 7+ years of Pharma/Biotech/CRO experience and regulatory compliance expertise (GMP, US NDA/EU MAA) to craft market-access strategies. Native Korea...

Seeking a skilled **Data Surveillance Analyst** in South Africa, Poland, or Lithuania to drive quality in clinical trials. You will analyze scientific data, develop **Data Surveillance Plans (DSPs)**, and review **Quality Tolerance Limits**. Requires 3+ years in CRO/Pharma, **SAS/SQL** experience...

We are seeking a Data Surveillance Analyst to join our global team in South Africa, Lithuania, or Poland. You will leverage your expertise in data analytics, SAS/SQL, and risk management to support centralized monitoring and data-driven processes within CRO/Pharma. Key responsibilities include de...

Lead global clinical trials as a Project Leader at Parexel, a top CRO. This home-based role requires 2+ years of CRO project management experience and a clinical degree. You will drive cross-functional teams, manage budgets and timelines, and bring life-changing treatments to market. Enjoy a supp...

Lead governance, risk, and compliance for Parexel’s global Data & Technology group as Director, Risk & Compliance Management. This UK-based, fully remote role requires deep expertise in QMS, SDLC, and vendor oversight within regulated environments. Drive inspection readiness and operational excel...

Lead clinical trials as a Local Study Associate Director with Parexel’s FSP team, working for a top pharmaceutical company. Based in Istanbul or Ankara with hybrid flexibility, you will manage cross-functional teams, ensure ICH-GCP compliance, and oversee site activities. Requires 3+ years in Dev...