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

3-5 years
€75,000 – €105,000 annually
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

Job Title: Manager, Clinical Monitoring (English and French Speaking)
Location: Remote, Spain (also open to UK, Hungary, Poland, Romania, Serbia, or Slovakia)
Job Type: Regular Full-time
Division: Precision for Medicine – Clinical Solutions
Requisition Number: 5769
Estimated Salary: €75,000 – €105,000 annually (based on experience and location)


Position Overview:
Precision for Medicine is hiring a Manager, Clinical Monitoring to lead and develop a team of CRAs across Europe. This leadership role is focused on people management, resource planning, quality improvement, and operational oversight for our growing clinical monitoring team. Candidates must be fluent in both English and French.


Key Responsibilities:

Team Leadership & Development:

  • Manage, mentor, and coach CRAs to maintain high-quality standards and foster career progression

  • Create strategic development plans and training programs

  • Conduct accompanied site visits and regular performance evaluations

  • Oversee onboarding and integration of new CRA hires

  • Advocate for team morale, accountability, and retention

Operational Oversight:

  • Collaborate with Project Managers and Clinical Trial Managers for effective resource allocation

  • Ensure CRA assignments are aligned with project phases and timelines

  • Monitor CRA compliance with SOPs, training, and systems usage

  • Track CRA performance metrics and recommend quality improvement actions

  • Represent the CRA team in cross-functional discussions

Quality Management:

  • Identify site or staff-related quality risks; recommend and support corrective action plans

  • Maintain and improve CRA processes, tools, and guidelines

  • Support audit readiness and ensure monitoring activities comply with ICH-GCP and regulatory standards

Recruitment & Planning:

  • Participate in CRA recruitment (CV screening, interviews)

  • Contribute to strategic workforce planning and resourcing discussions

Other Duties:

  • Represent Precision for Medicine in internal and external settings

  • Domestic and international travel (up to 25%)


Minimum Qualifications:

  • Bachelor's degree (scientific/healthcare discipline preferred) or equivalent experience

  • Fluent in English and French

  • At least 7+ years in clinical operations or data management

  • Minimum of 5 years of on-site CRA monitoring experience

  • 3–5 years of direct CRA supervisory experience, including:

    • Performance evaluation and staff development

    • Training plan development and implementation


Preferred Experience:

  • Strong monitoring background in oncological clinical trials

  • Familiarity with electronic data capture systems, EMRs, and eCRFs

  • Demonstrated knowledge of GCP, regulatory guidelines, and remote monitoring best practices


Key Competencies:

  • Excellent interpersonal and leadership skills

  • Strong organizational and analytical abilities

  • High emotional intelligence and a passion for people development

  • Ability to prioritize, multitask, and solve site-level operational challenges

  • Strong communication and presentation skills

  • Commitment to continuous process and quality improvement


Important Notice:
Precision for Medicine conducts all hiring through direct communication with its recruitment team and a formal interview process. Be cautious of unauthorized employment offers from external sources.