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Clinical Project Manager (Freelance Position) - Extensive Experience In Lung, Breast Or Gastro Oncology Or Radiopharmaceuticals Required

0-2 years
Not Disclosed
10 Oct. 2, 2025
Job Description
Job Type: Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

🧾 Job Title: Clinical Project Manager (Freelance)

🏢 Company: Ergomed Group
📍 Location: Remote
🕒 Employment Type: Full-time (Freelance)
📂 Department: Project Management CRO


🌍 About Ergomed

Ergomed Group is a rapidly expanding full-service mid-sized CRO specializing in Oncology and Rare Disease, with operations across Europe, North America, and Asia.

  • Founded: 1997

  • Culture: International, collaborative, and employee-centric

  • Focus: Delivering high-quality clinical services while positively impacting patient lives


🧾 Job Description

We are recruiting a contract Clinical Project Manager with extensive experience in global trials within the following oncology indications:

  • Radiopharmaceuticals

  • Gastrointestinal cancer

  • Lung cancer

  • Breast cancer

The role involves end-to-end project management for clinical trials, ensuring alignment with industry standards, sponsor expectations, and Ergomed quality requirements.


🔹 Key Responsibilities

  • Ensure projects are delivered on time, within budget, and within agreed scope

  • Maintain industry, sponsor, and Ergomed quality standards throughout project execution

  • Liaise with project team members, provide training, and ensure proper task allocation

  • Develop, review, and edit project plans to align with goals and milestones

  • Organize and facilitate project meetings covering study initiation, execution, and closure

  • Serve as primary point of contact with sponsors and Ergomed Senior Management for project updates

  • Represent Ergomed at external meetings, liaising with scientific/medical experts, CROs, and sponsors (e.g., EC/IRB committees)

  • Develop, review, and edit SOPs to ensure regulatory compliance

  • Develop study-related training programs for team members

  • Contribute to bid defense activities as needed


🎓 Qualifications

  • Experience as a Project Manager in international clinical trials within a CRO environment

  • Extensive experience with global trials in radiopharmaceuticals, gastrointestinal cancer, lung cancer, or breast cancer

  • Bid defense experience

  • Strong analytical, organizational, and communication skills

  • Bachelor’s degree in a science-related discipline


🌟 Why Ergomed

Our core values define how we operate:

  • Quality

  • Integrity & Trust

  • Drive & Passion

  • Agility & Responsiveness

  • Belonging

  • Collaborative Partnerships

Join Ergomed to lead global oncology trials with scientific rigor, operational excellence, and meaningful patient impact.