Clinical Project Manager, Phase 1 Oncology, East Coast

Proven Recruiting, Inc.

Exton (PA)

Remote

USD 62,000 - 90,000

Full time

14 days+

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Job summary

Proven Recruiting, Inc. seeks a Clinical Project Manager for a remote, East Coast–based contract role to lead Phase I oncology trials from startup through completion with high visibility and ownership.

The position supports a 12-18 month engagement, offering $45-$65/hr. East Coast residence and strong ICH-GCP/China GCP knowledge are required, with CRO/biotech experience preferred.

Qualifications

  • 5+ years of clinical project management experience in CRO/pharma/biotech environments.
  • Direct experience managing Phase I oncology trials is required.
  • Strong knowledge of ICH-GCP, China GCP, regulatory requirements, and clinical operations.

Responsibilities

  • Lead startup activities: contract review, resource planning, investigator meetings, communication plans, and MOPs.
  • Oversee study timelines, budgets, enrollment, site activation, monitoring, sponsor communications, and deliverables for successful execution.
  • Ensure compliance with protocols and regulatory requirements while maintaining data quality and trial master file integrity.

Skills

Clinical project management
Budget management
Timeline coordination
Regulatory compliance

Job description

Clinical Project Manager - Remote (East Coast Required) - $45-$65/hr

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.

Who you are:
  • 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.
What you’ll do:
  • 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.
What does this position pay?

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.

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