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

3-5 years
RSD 7,000,000 – RSD 10,000,000 per year
10 July 7, 2025
Job Description
Job Type: Remote 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, Serbia

Estimated Salary: RSD 7,000,000 – RSD 10,000,000 per year (based on senior clinical operations roles in Serbia)

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

Position Summary:
Precision for Medicine is hiring a Manager, Clinical Monitoring (GCM) to lead, develop, and support a team of Clinical Research Associates (CRAs) across Europe. This fully remote role may be based in Serbia or nearby countries, and is ideal for experienced clinical research professionals with a strong track record in oncology trials and CRA supervision.

Key Responsibilities:

  • Develop strategic plans to optimize CRA performance and team goals

  • Assign project resources effectively based on project phase and complexity

  • Collaborate with Clinical Trial Managers and Operations teams to meet project/site requirements

  • Mentor and coach CRA staff, promote professional development, and reduce turnover

  • Conduct site visits, assess CRA performance, and provide tailored feedback

  • Identify and manage quality risks, implement corrective action plans

  • Ensure CRAs have access to required tools, training, and systems

  • Oversee CRA administrative compliance (SOPs, time & expense, documentation)

  • Drive continuous process improvement and support recruitment and onboarding of new CRAs

  • Lead or participate in the interview process, onboarding, and training sessions

Qualifications:

  • Bachelor's or postgraduate degree in life sciences or healthcare

  • Fluent in both English and French

  • Minimum 7 years of clinical operations experience, including 5+ years of on-site monitoring

  • Strong oncology trial experience

  • 3–5 years of experience managing or supervising CRAs

  • Proven ability to develop effective training and evaluation programs

  • Willingness to travel up to 25% internationally

Skills and Competencies:

  • Strong knowledge of ICH-GCP, regulatory guidelines, and CRA operations

  • Ability to manage remote teams and support performance metrics

  • High emotional intelligence and a proactive leadership mindset

  • Skilled at problem-solving, organizing priorities, and driving improvement

  • Confident in conducting formal presentations to various stakeholders

  • Proficiency in systems like EMRs, EDCs, and Microsoft Office

Why Precision for Medicine?

  • Join a growing, innovative team shaping the future of clinical trials

  • Work remotely with flexibility across borders

  • Lead impactful oncology projects and drive real clinical change

  • Enjoy a culture focused on development, quality, and performance