Parexel - United States

Senior Regulatory Affairs Consultant – Regulatory Labeling Strategist sought by Parexel Consulting to lead global labeling strategy for biopharma clients. This remote role requires 5-7 years’ industry experience, including 2+ years in global labeling with strategic leadership. You will drive CCDS...

Parexel seeks a remote **Data Management Lead** (Data Manager II) based in the Continental US. You will oversee study data delivery timelines, including Go-Live and Final Database Lock, while collaborating with global cross-functional teams. This role demands 6+ years of clinical research experie...

Senior Clinical Research Associate / CRA II – Oncology. Join Parexel to drive global clinical trials with 60-80% travel across the US. Leverage 3+ years of site monitoring experience (2+ in Oncology preferred) and deep ICH/GCP knowledge. Ensure patient safety, manage investigator sites, and enjoy...

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...

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, ...