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

3-7 years
RON 190,000 – RON 280,000 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, Romania

Estimated Salary: RON 190,000 – RON 280,000 per year (approximately €38,000 – €56,000/year), based on Romanian clinical operations leadership benchmarks

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

Position Summary:
Precision for Medicine is expanding its European operations and seeking a Manager of Clinical Monitoring (GCM) to join the team remotely from Romania. This role is ideal for experienced clinical research professionals passionate about team leadership, CRA development, and high-quality clinical trial delivery—especially in oncology.

Key Responsibilities:

  • Create development plans and optimize CRA operations to meet project and departmental objectives

  • Allocate CRA resources based on project requirements and lifecycle phase

  • Collaborate with project and clinical leads to fulfill site and staffing needs

  • Coach, manage, and mentor CRA team members to meet high-performance standards

  • Conduct accompanied site visits and assess CRA capabilities

  • Identify and address quality risks with corrective action plans

  • Ensure availability of systems, tools, training, and materials to all CRAs

  • Maintain updated documentation, SOPs, and administrative systems

  • Streamline CRA processes to improve consistency and operational efficiency

  • Participate in hiring, onboarding, and training new CRAs

  • Provide input on performance evaluations and assist with team planning

  • Represent Precision for Medicine with professionalism across internal and external interactions

Qualifications:

  • Bachelor’s or postgraduate degree in science or healthcare (or equivalent experience)

  • Fluent in English and French

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

  • Proven experience in oncology clinical trials

  • 3–5 years in a CRA supervisory/management role

    • Demonstrated success in CRA development programs and evaluation frameworks

  • Willingness to travel (~25%), both domestically and internationally

Skills and Competencies:

  • Strong knowledge of ICH-GCP, local regulations, and CRA best practices

  • High emotional intelligence with a passion for mentoring and team growth

  • Experience with EDC and EMR systems

  • Capable of strategic planning, problem-solving, and motivating remote teams

  • Strong presentation, communication, and organizational skills

  • Committed to continuous improvement and operational excellence