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

3-5 years
€55,000 – €75,000 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, Slovakia

Estimated Salary: €55,000 – €75,000 per year (based on comparable clinical operations management roles in Slovakia)

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

Position Summary:
Precision for Medicine is expanding its European team and is seeking a skilled Manager of Clinical Monitoring (GCM) to lead and support Clinical Research Associates (CRAs) across Europe. This fully remote position, open to professionals based in Slovakia and other specified countries, involves oversight, coaching, and operational optimization of CRA teams working in cutting-edge therapeutic trials, especially oncology.

Key Responsibilities:

  • Generate strategic development plans and drive high-quality CRA team performance

  • Oversee resource allocation, ensuring optimal staffing across all study phases

  • Collaborate with project managers and operations leaders to align on resourcing and timelines

  • Mentor, support, and coach CRAs while driving individual performance and development

  • Conduct accompanied visits and troubleshoot CRA-specific issues on-site

  • Identify performance risks and propose corrective action plans to leadership

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

  • Review and approve CRA administrative documentation (e.g., SOPs, timesheets)

  • Refine internal processes and procedures to improve quality and efficiency

  • Support CRA recruitment, onboarding, and development programs

  • Represent Precision for Medicine with professionalism and a leadership mindset

Required Qualifications:

  • Bachelor’s, postgraduate, or equivalent degree in a scientific or healthcare discipline

  • Fluent in both English and French

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

  • Proven leadership experience with 3–5 years managing CRAs, including coaching and performance review

  • Strong background in oncology trials

  • Willingness and ability to travel domestically/internationally (~25%)

Skills and Competencies:

  • In-depth knowledge of ICH-GCP, local regulations, and SOPs

  • High emotional intelligence with a strong passion for team development

  • Strong understanding of EDCs, EMRs, and monitoring platforms

  • Effective in strategic planning, problem-solving, and performance analysis

  • Ability to deliver formal presentations confidently and effectively

  • Commitment to continuous improvement and service excellence

Why Precision for Medicine?

  • Work in a collaborative, remote-first environment

  • Contribute to impactful oncology trials across Europe

  • Gain career growth opportunities in a high-performance team

  • Be part of an organization that values people development, innovation, and excellence