Parexel - United States, Remote work

Vice President, Project Leadership role driving strategic oversight for clinical trial delivery across the US. Seeking expert project management experience in healthcare or CROs, with proven global matrix leadership. You will lead Directors, ensure financial and quality targets, and foster authen...

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 detail-oriented **HCP Contract Specialist** to manage end-to-end contracting for healthcare professionals and institutions in the **United States**. This role requires strong project management, customer service, and compliance skills, collaborating with legal, finance, and commercial t...

Seeking a Site and Monitoring Health Lead for the Northeast US. This site-facing FSP role ensures GCP compliance and CRO oversight for multinational clinical trials. Requires significant CRO monitoring oversight, Lead CRA experience, and up to 50% travel. Join a team dedicated to inspection-ready...

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, ...

Lead global clinical trials for biotech clients in this remote US role. Utilize your project management expertise within a CRO or pharma setting to deliver patient-focused studies. Drive operational excellence while enjoying a supportive, flexible environment with diverse therapeutic challenges.

Lead our Site and Monitoring Health team, ensuring clinical trial quality and CRO oversight. This site-facing role requires significant monitoring and lead CRA experience, with up to 50% travel. Apply your expertise in GCP, risk-based oversight, and innovative problem-solving within a US-based FS...

Join Parexel Consulting as a Senior Regulatory Affairs Consultant specializing in Regulatory Intelligence. Utilize your 5-7 years of experience to provide strategic intelligence, helping biopharma and device clients navigate FDA and global regulations. This remote US role offers flexible work, ca...

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...

Join our team as a Remote Meeting Specialist, managing high-quality international events for the pharmaceutical industry. Utilize your 3+ years of pharma event expertise to plan and execute seamless in-person and virtual meetings. This full-time role offers a competitive salary with an annual bon...