Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Thermo Fisher Scientific

Clinical Team Manager – Internal Medicine

Thermo Fisher Scientific

Clinical 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.

Posted 8/2/2026full-timeRemote • North Carolina • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit
Core 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 resume
Applicant 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 & technologies
Google 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