Clinical Project Manager, Phase Oncology, East Coast

Have deep expertise leading Phase I oncology clinical trials? This is a long-term 12-18 month contract opportunity with our client, an innovative clinical research organization, where you'll drive complex early-phase oncology studies from startup through completion while working remotely with high visibility and ownership.

• 5+ years of clinical project management experience within a CRO, pharmaceutical, or biotechnology environment.
• Direct experience managing Phase I oncology clinical trials is required.
• Strong knowledge of ICH-GCP, China GCP, clinical trial operations, investigational product management, and regulatory requirements.
• Proven experience managing study timelines, budgets, sponsors, investigators, and cross-functional clinical teams.
• Must reside on the East Coast and be able to work effectively in a remote environment.

• Lead project startup activities including contract review, resource planning, team formation, investigator meetings, communication plans, and master operating plans (MOPs).
• Oversee study timelines, budgets, enrollment, investigational product planning, site activation, monitoring activities, sponsor communications, and project deliverables to ensure successful study execution.
• Ensure compliance with protocols, SOPs, ICH-GCP/China GCP requirements, and applicable regulations while maintaining data quality, inspection readiness, and trial master file integrity.

Compensation is determined by several factors which may include skillset, experience level, and education. The expected range for this role is $45-$65 per hour.

Please note this range is an estimate and actual pay may vary based on qualifications and experience.

Note:

We actively support and promote people of various backgrounds, from race, religion, gender to geographical area, university, lifestyle, and personality type. Proven Recruiting is minority-owned, majority women, and is a strong advocate for diversity and inclusion in the broader community.