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

3-7 years
HUF 17,500,000 – HUF 25,000,000 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, Hungary

Estimated Salary: HUF 17,500,000 – HUF 25,000,000 per year (approx. €45,000 – €65,000/year equivalent), based on local benchmarks for clinical operations leadership roles in Hungary

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

Position Summary:
Precision for Medicine is seeking an experienced Manager of Clinical Monitoring (GCM) to join its European team remotely from Hungary. This leadership role focuses on the oversight, development, and performance management of Clinical Research Associates (CRAs), ensuring consistent quality delivery in global clinical trials, particularly in the oncology domain.

Key Responsibilities:

  • Lead strategic development and performance improvement plans for CRAs

  • Support project resource allocation and tracking across all trial phases

  • Ensure CRA teams are equipped with tools, training, and guidance needed for successful execution

  • Collaborate with Project and Clinical Team Leads to align staffing and site needs

  • Mentor and coach CRA staff, conducting regular assessments and accompanied site visits

  • Maintain CRA compliance with SOPs, documentation, and system updates

  • Refine procedures and drive process efficiencies within CRA operations

  • Participate in recruitment and onboarding of CRA staff

  • Contribute to performance evaluations and feedback cycles

  • Promote employee engagement, retention, and satisfaction within the CRA workforce

  • Represent Precision for Medicine with professionalism in all engagements

Required Qualifications:

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

  • Fluent in English and French

  • Minimum 7 years of clinical research experience, including at least 5 years of on-site monitoring

  • Minimum 3–5 years in a supervisory or CRA management role

  • Strong background in oncology clinical trials

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

Skills and Competencies:

  • Deep understanding of ICH-GCP, local regulatory frameworks, and SOPs

  • Strong emotional intelligence and people management skills

  • Hands-on experience with EDC, EMRs, and remote monitoring

  • Proven organizational, leadership, and problem-solving abilities

  • Ability to develop and execute effective training programs for clinical staff

  • Excellent interpersonal and communication skills

  • Comfortable conducting formal presentations to diverse audiences

Why Join Precision for Medicine?

  • Work remotely in a high-impact role across Europe

  • Help shape and develop CRA teams in global oncology trials

  • Grow your career in a collaborative, innovation-driven environment

  • Be part of an organization committed to employee development and operational excellence