Parexel - United States, Remote work

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 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...

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, ...

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 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...

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...