Parexel - United States, IT - Software Development

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...

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 early-phase clinical trials as a **Project Manager** at Parexel, driving cross-functional teams to deliver life-changing treatments. This remote role requires 2+ years of PM experience (or 3-5 in related fields), ICH-GCP knowledge, and strong leadership. You will own sponsor relationships, m...

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...

Join Parexel as a Clinical Research Associate (CRA) in Early Development Oncology, covering the Northeast US. Leverage your 3+ years of site monitoring experience and GCP/FDA expertise to oversee clinical trials from activation to database lock. Enjoy 60-80% travel, flexible work arrangements, an...

Seeking a Scientist III - Analytical Chemist (Drug Product) for a long-term FSP role in Rahway, NJ. This position requires hands-on expertise in UPLC, HPLC, GC, and Empower software for drug product analysis. Ideal candidates possess a BS/MS with relevant experience and strong skills in method de...

Seeking a Clinical Laboratory Study Manager in the US to drive precision medicine strategies. Requires 6+ years of clinical research experience, a life sciences degree, and expertise in GCP/ICH guidelines. You will manage sample logistics, develop study documents, and collaborate with cross-funct...

Senior Regulatory Consultant sought to lead global regulatory strategy and program management for biopharma clients. Leverage 7+ years of experience in regulatory affairs and submissions (IND/BLA/MAA) to drive product development. This remote role offers mentorship, diverse therapeutic exposure, ...

Join Parexel in Newton, MA, as a Principal Statistical Programmer. Lead statistical programming for clinical trials, ensuring compliance with CDISC and FDA regulations. Utilize advanced SAS programming to analyze data across diverse therapeutic areas. Benefit from career growth, flexible work, an...

Lead clinical sample logistics and data operations in this remote US role. Utilize your expertise in Python, R, or SQL to develop tracking tools and ensure data integrity for biomarker studies. This position requires strong programming skills and 6+ years of clinical research experience to stream...