Lead Medical Project Coordinator

Thermo Fisher Scientific

Lead Medical Project Coordinator managing the evaluation and delivery of medical projects at Thermo Fisher Scientific. Collaborating globally to improve health outcomes through innovative solutions.

Posted 7/15/2026full-timeRemote • 🇵🇭 PhilippinesSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates extensive clinical safety experience with a strong focus on project management, safety data evaluation, and compliance with GCPs in clinical trials. Capable of leading teams, mentoring new members, and effectively communicating complex information.

Highest-signal resume keywords

Clinical Safety ExperienceGCP KnowledgeProject Management SkillsSafety Data EvaluationMentoring and Training

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 Research MonitoringPharmacovigilanceSafety Data TrendingDrug Development KnowledgeBiostatisticsData ManagementSafety ReportingBudget Management

Soft Skills

Problem SolvingCritical ThinkingOral CommunicationWritten Communication

Certifications & Qualifications

Bachelor's Degree in NursingLicensed RNPhysician's Assistant

Industry Keywords

Medical MonitoringClinical TrialsSafety Management PlanOperational Risks

About the role

Key responsibilities & impact

Lead the management, coordination and evaluation of medical projects
Work independently to perform and/or lead first pass review of safety data
Proactively identify and resolve/escalate potential issues
Initiate and lead initiatives to improve processes regarding medical monitoring
Manage project implementation, coordination, maintenance and close out
Serve as the primary point of contact for clinical project teams
Create and maintain safety and medical management plan(s)
Monitor project financial status and escalates any financial or operational risks
Train and develop new team members
Resolve complex problems through in-depth evaluation of various factors

Requirements

What you’ll need

Bachelor's degree in Nursing or related Health Sciences (Physician's Assistant) or licensed RN
8+ years clinical safety experience (clinical research monitoring, or pharmacovigilance or combination of both)
Superior knowledge of GCPs for medical oversight of clinical trials
Advanced knowledge of drug development and safety reporting
Extensive knowledge of safety data trending to include coding
Good knowledge of biostatistics, data management and clinical procedures
Exceptional problem solving and critical thinking skills
Exceptional project management and budget skills
Excellent mentoring skills and ability to train and lead others
Exceptional oral and written communication skills

Benefits

Comp & perks

Health and wellbeing support
Resources for individual career goals
Opportunities for collaboration and development