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Clinical Trial Physician – Phase I, EMEA
Thermo Fisher Scientific. Provide medical leadership to study teams .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in medical leadership for clinical trials, including protocol development, medical monitoring, and compliance with SOPs and GCP. Proficient in interpreting clinical data and providing medical training while ensuring subject safety and effective communication with stakeholders.
Highest-signal resume keywords
Medical DoctorClinical Trial Protocol DevelopmentMedical MonitoringKnowledge of SOPs and GCPInterpersonal Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Trial Protocol DevelopmentMedical MonitoringData InterpretationRegulatory Document PreparationClinical Document Review
Soft Skills
Proactive Problem-SolvingNegotiation SkillsStrong Communication SkillsInterpersonal SkillsTeam Leadership
Industry Keywords
Clinical TrialsStudy ProtocolsMedical ValidityStudy Subject SafetyCross-Functional Collaboration
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Provide medical leadership to study teams
- Create clinical trial protocols using the latest scientific information
- Contribute to site selection and review and approval of study protocols and amendments, CSRs, ICFs, CRFs, protocol deviation decisions, and other clinical documents
- Perform real-time medical monitoring of clinical studies
- Ensure medical validity of primary endpoints and study subject safety
- Proactively escalate and correct medical issues in consultation with the Global Medical Indication Lead
- Interpret clinical trial data for regulatory documents, manuscripts, and other publications
- Act as medical point of contact for internal and external stakeholders
- Interact with investigators and answer questions from IRBs and Health Authorities
- Prepare and present material to study executives and independent safety committees when applicable
- Provide medical training to site staff and CRA training in new indications
- Ensure compliance with medical aspects of studies by applying relevant SOPs and GCP
- Collaborate with cross-functional study team members to clarify medical risks, issues, and results
- Harmonize answers, eligibility decisions, and protocol deviation decisions when multiple physicians work on a protocol
Requirements
What you’ll need- Medical Doctor
- Relevant specialty education preferred, such as neurology, hematology, dermatology, immunology, rheumatology, internal medicine, or pediatrics
- Some experience in industry preferred
- Excellent English, written and spoken
- Ability to travel
- Proven interpersonal skills to lead a study team and provide medical advice and evaluations
- Proactive problem-solving and negotiation skills
- Strong communication skills for collaboration in a cross-functional, matrix structure
- Knowledge and application of relevant SOPs and GCP
- Ability to exercise judgment and escalate issues immediately when needed
Benefits
Comp & perks- Healthy and balanced work environment
- Collaboration and professional development opportunities
- Ability to travel