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Clinical Team Manager – Internal Medicine
Thermo Fisher ScientificClinical Team Manager responsible for managing clinical trials and ensuring quality deliverables for healthcare innovations. Leading teams and collaborating with departments to meet project requirements and timelines.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical operations and quality for complex studies, ensuring compliance with ICH GCP and timely delivery of clinical milestones. Proficient in developing clinical tools and collaborating effectively with project managers and clients.
Highest-signal resume keywords
Clinical Trial OperationsStudy ManagementClinical MonitoringICH GCP ComplianceClinical Deliverable Achievement
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ResearchMonitoring Plan DevelopmentData Quality Plan DevelopmentTrial Master File ManagementClinical Activity Timeline Preparation
Soft Skills
CollaborationPresentation SkillsOrganizational Skills
Certifications & Qualifications
Bachelor's Degree
Industry Keywords
HealthcareNursingMedicineClinical OperationsQuality Assurance
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Manage all clinical operational and quality aspects of allocated studies, of moderate to high complexity, in compliance with ICH GCP.
- Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan.
- Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central).
- Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
- Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics.
Requirements
What you’ll need- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- 5+ years of relevant experience in clinical research, including clinical trial operations, study management, clinical monitoring, or related clinical research activities.
- Transferable experience in healthcare, nursing, medicine, or related disciplines
Benefits
Comp & perks- Health insurance
- Flexible work arrangements
- Paid time off
- Professional development