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Strong fit if you have led clinical or biotech projects—ideally oncology or late-phase trials—and can drive remote/home-based coordination for a global CRO. Thin public review data means culture fit is best validated in interviews; operational rigor and clear sponsor communication matter most.
As project leadership on biotech clinical trials in oncology at Parexel, a typical day centers on cross-functional trial delivery: aligning timelines with medical, data, and site teams; tracking enrollment and protocol milestones; escalating risk to quality and patient safety; and reporting status to sponsors. Expect vendor and investigator coordination, issue logs, and documentation that keeps oncology studies audit-ready.
Pair free health-sciences learning with hands-on trial ops, ICH-GCP familiarity, and oncology protocol literacy.
The title flags home-based/future needs while the listing location is Five Points, Wake County; confirm hybrid expectations with the recruiter.
Parexel is a contract research organization that runs clinical trials for pharma and biotech clients to advance drug development.
Saylor Health Sciences courses (free) and Coursera audit-track healthcare courses (free to learn) are the listed resources—no paid cert prices appear in the data.
Website: parexel.com
Parexel is an American contract research organization. It conducts clinical trials on behalf of its pharmaceutical and biotechnology clients to expedite drug development and clinical trial progress.
Public cache only — not an employee review.
Parexel is hiring a Project Leadership professional to oversee biotech clinical trial programs within our Oncology division. This full-time position is based in Five Points, Wake County and plays a central role in managing complex research initiatives from planning through completion, directly impacting the development of new cancer therapies. About the Role You'll direct clinical trial programs across the full lifecycle, leading cross-functional teams and managing the intricate relationships between sponsors, clinical sites, regulatory agencies, and internal stakeholders. Your project leadership will encompass budget oversight, timeline management, risk mitigation, and compliance execution—ensuring each oncology program meets quality standards and delivers measurable value to our biotech partners and their patients. What You'll Do Oversee end-to-end execution of oncology clinical trial programs within defined timelines and budgets Lead and coordinate cross-functional project teams across internal and external partners Manage regulatory submissions, compliance requirements, and FDA milestone tracking Develop project plans, resource schedules, and risk management strategies Monitor program progress, identify bottlenecks, and implement corrective measures Maintain transparent communication with clients, sponsors, and senior leadership on program status and outcomes What We're Looking For Demonstrated project or program management experience within biotech, clinical research, or pharmaceutical settings Strong background in oncology clinical trial design, conduct, or oversight Proficiency with regulatory frameworks including FDA regulations and ICH-GCP guidelines Proven ability to lead teams, manage stakeholders, and influence across organizations Experience managing multi-million-dollar budgets and complex timelines Exceptional communication and problem-solving capabilities About Parexel Parexel is a global leader in clinical development and commercialization services for the biotech and pharmaceutical industries. Our Biotech Division brings specialized expertise in oncology research, supporting the development of breakthrough therapies that improve patient outcomes worldwide. How to Apply Apply directly through this listing to join our Project Leadership team in Five Points, Wake County.
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