Senior Medical Project Coordinator

Thermo Fisher Scientific

Senior Medical Project Coordinator managing, coordinating, and evaluating medical projects for Thermo Fisher Scientific. Ensuring process consistency and compliance across multiple programs with a focus on safety data review.

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

Core Competencies

Role fit

Core Competencies

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Demonstrates advanced knowledge of GCPs, clinical safety, and drug development, with a strong ability to manage medical projects and ensure compliance. Proven skills in project management, financial oversight, and effective communication within clinical project teams.

Highest-signal resume keywords

Clinical Safety ExperienceGCP KnowledgeProject Management SkillsSafety Data TrendingProblem Solving Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research MonitoringPharmacovigilanceSafety Data ReviewBiostatisticsData ManagementBudget ManagementMedical Management PlansSafety ReportingCoding ConsistenciesRisk Management

Soft Skills

Critical ThinkingMentoring SkillsOral CommunicationWritten CommunicationAttention to Detail

Certifications & Qualifications

Bachelor's Degree in NursingLicensed RNPhysician's Assistant

Industry Keywords

Clinical TrialsDrug DevelopmentSafety TrendsComplianceStakeholder Collaboration

About the role

Key responsibilities & impact

Manage, coordinate, and evaluate medical projects for one or more programs
Collaborate with management and other stakeholders for process consistency and compliance
Perform first pass review of safety data
Review data for safety trends, coding consistencies, and potential follow up with investigator sites
Proactively identify any potential issues and resolve or escalate as appropriate
Review safety data and provide summations for safety review meetings
Manage project implementation, coordination, maintenance and close out of assigned studies
Serve as the primary point of contact for clinical project teams on studies
Create and maintain medical management plan(s) on studies
Monitor the project financial status and unit forecasting
Coordinate staff projections based on contract values and actual hours used
Escalate any financial and/or operational risks and attend risk management meetings
Resolve complex problems through in-depth evaluation of various factors and offers solutions
Present at business development, client, and investigator meetings.

Requirements

What you’ll need

Bachelor's degree in Nursing or related Health Sciences (Physician's Assistant) or licensed RN
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years)
5+ years clinical safety experience (clinical research monitoring or pharmacovigilance or combination of clinical research monitoring and pharmacovigilance)
Advanced knowledge of GCPs for medical oversight of clinical trials
Knowledge of drug development and safety reporting
Advanced knowledge of safety data trending to include coding
Working knowledge of biostatistics, data management and clinical procedures
Excellent problem solving and critical thinking skills
Excellent project management and budget skills
Effective mentoring skills and ability to train and lead others
Strong oral and written communication skills
Strong attention to detail
Ability to work in a collaborative team environment
Ability to maintain a positive and professional demeanor in challenging circumstances.

Benefits

Comp & perks

Health and wellbeing support for employees
Professional development opportunities