Freelance Clinical Project Manager
@ EPM Scientific

Hybrid
$90,000
Hybrid
Contractor
Posted 21 days ago

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XXXXXXXXXX XXXXXXXXXXX XXXXXX******* @epmscientific.com
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Job Details

Freelance Clinical Project Manager

EPM Scientific is partnering with a Biotechnology company to support upcoming Oncology Trials in the EU. This is a 12-month contract at 0.8-1 FTE on a remote basis.

Contract Conditions

Start Date: ASAP Location: European Union (Remote) Contract: 12-Month Contract, 0.8 - 1 FTE

Project Overview

Oncology - Phase 3 Global Trial

Key Responsibilities

  • Lead and oversee global clinical trial sites ensuring compliance with GCP, protocol, and regulatory requirements.
  • Serve as the primary contact for internal and external stakeholders.
  • Support site initiation, monitoring, and close-out activities.
  • Ensure timely and accurate documentation, data collection, and reporting.
  • Collaborate with CRAs, Medical Monitors, Regulatory Affairs, and Data Management teams.
  • Contribute to risk-based monitoring and audit readiness strategies.

Requirements

  • 5+ years of clinical project management experience, preferably in Oncology.
  • Strong knowledge of ICH-GCP, EMA & FDA regulatory standards.
  • Proven ability to work independently and manage global clinical operations.
  • Excellent communication and organizational skills.
  • Eligibility to work as a Freelancer in your country of residence.

Key skills/competency

  • Clinical Trials
  • Oncology
  • Project Management
  • GCP
  • Regulatory Compliance
  • Stakeholder Management
  • Documentation
  • Risk Management
  • Communication
  • Cross-functional Collaboration
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How to Get Hired at EPM Scientific

🎯 Tips for Getting Hired

  • Research EPM Scientific's culture: Investigate mission, values, and employee reviews.
  • Customize your resume: Tailor it to highlight clinical and oncology expertise.
  • Highlight trial experience: Emphasize global clinical trial management skills.
  • Prepare for interviews: Practice regulatory and GCP compliance scenarios.

📝 Interview Preparation Advice

Technical Preparation

Review ICH-GCP guidelines documentation.
Study EMA and FDA regulatory frameworks.
Practice trial site data management tools.
Prepare risk-based monitoring case studies.

Behavioral Questions

Describe a challenging project management situation.
Explain your approach to stakeholder conflicts.
Discuss a time you met tight deadlines.
Share experiences working with cross-functional teams.

Frequently Asked Questions