Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

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

Precision For Medicine
Precision For Medicine
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