Medical Project Coordinator

Thermo Fisher Scientific

. Coordinate and review safety data using line listings, company dashboards, and visualization tools .

Posted 9/24/2026full-timeRemote • SerbiaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical safety and pharmacovigilance, with a strong focus on data management, safety data trending, and compliance with GCPs. Capable of effective communication and collaboration in clinical research settings, while providing training and mentoring to project teams.

Highest-signal resume keywords

Clinical Safety ExperienceGCP KnowledgeData ManagementProblem-Solving SkillsCommunication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research MonitoringPharmacovigilanceSafety Data TrendingBiostatisticsSAE Processing

Soft Skills

Attention to DetailCritical ThinkingCollaborationProfessional Demeanor

Tools & Technologies

Visualization ToolsCompany Dashboards

Certifications & Qualifications

Bachelor’s Degree in NursingLicensed RNPhysician's Assistant

Industry Keywords

Drug DevelopmentSafety ReportingClinical Trials

About the role

Key responsibilities & impact

Coordinate and review safety data using line listings, company dashboards, and visualization tools
Review data for safety trends, coding consistencies, and potential investigator-site follow-up
Identify, resolve, or escalate issues
Provide summations for safety review meetings
Review designated sections of aggregate reports
Help create and review safety and medical management plans for studies
Help manage routine project implementation, forecasting, coordination, metrics, and budget considerations
Monitor data-review status and escalate delays and risks to stakeholders and study leads
Present at business development, client, and investigator meetings
Participate in strategy and business development calls
Resolve complex problems through in-depth evaluation and offer solutions
Serve as primary point of contact for clinical/data management project teams
Assist management with training and mentoring

Requirements

What you’ll need

Bachelor’s degree in nursing or related Health Sciences (Physician's Assistant) or licensed RN
2+ years of experience, including 2+ years of clinical safety experience in clinical research monitoring, pharmacovigilance, or a combination of both
Knowledge of GCPs for medical oversight of clinical trials and SAE processing
Knowledge of drug development and safety reporting
Knowledge of safety data trending, including coding
Working knowledge of biostatistics, data management, and clinical procedures
Strong problem-solving and critical-thinking skills
Good oral and written communication skills
Good attention to detail
Ability to work collaboratively and maintain a positive, professional demeanor
Ability to work with computer software
Ability to meet physical, environmental, attendance, multitasking, and communication requirements
Equivalency through a combination of appropriate education, training, and/or directly related experience may be considered

Benefits

Comp & perks

Global team environment
Collaboration and development opportunities
Exposure to scientific excellence and innovation