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Manager, Clinical Monitoring (English And French Speaking) - Clinical Trial Services

3-5 years
PLN 450,000 – PLN 600,000 per year
10 July 7, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Manager, Clinical Monitoring (English and French speaking) – Clinical Trial Services
Location: Remote, Poland

Estimated Salary: PLN 450,000 – PLN 600,000 per year (based on industry standards for senior-level clinical operations roles in Poland)

Job Type: Regular, Full-time
Division: Precision for Medicine
Business Unit: Clinical Solutions

Position Summary:
Precision for Medicine is expanding! We’re seeking a Manager, Clinical Monitoring (GCM) to join our European team. This fully remote role may be based in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia. The GCM will be responsible for managing, mentoring, and developing CRAs while ensuring high-quality operational delivery across clinical trials.

Key Responsibilities:

  • Lead and mentor a team of CRAs, ensuring alignment with Precision’s standards and quality expectations

  • Drive performance through strategic oversight, development planning, and resource management

  • Support CRA resource allocation in collaboration with project and clinical operations teams

  • Conduct accompanied site visits, provide feedback, and identify developmental needs

  • Monitor CRA compliance, including SOPs, systems, and training requirements

  • Participate in CRA hiring, onboarding, and ongoing training

  • Manage departmental KPIs and contribute to continuous improvement initiatives

  • Communicate with leadership on staff performance, development plans, and any concerns

Qualifications:

  • Bachelor’s or postgraduate degree in a scientific or healthcare-related field

  • Fluent in both English and French

  • Minimum 7 years in clinical operations or data management, with at least 5 years of on-site monitoring experience

  • Strong background in oncology trials

  • 3–5 years of experience directly supervising CRAs

  • Experience designing development programs and competency evaluations

Skills and Competencies:

  • Deep knowledge of ICH-GCP, regulatory standards, and electronic systems (e.g., EDC, EMR)

  • Strong interpersonal, leadership, and coaching skills

  • Excellent organizational and decision-making ability

  • Passion for people development and emotional intelligence

  • High standards of professionalism, initiative, and customer service

  • Ability to manage remote teams and travel up to 25% internationally

Why Join Us:

  • Be part of a rapidly growing team with global exposure

  • Lead high-impact oncology trials with cutting-edge clinical research tools

  • Work remotely while collaborating with a diverse and talented international team

Note:
This is a remote position based in Poland, but candidates from nearby countries (UK, Spain, Hungary, Romania, Serbia, Slovakia) are also welcome to apply.