Medical Project Coordinator

Thermo Fisher Scientific

Medical Project Coordinator supporting drug safety operations with compliance in clinical trials. Reviewing safety data, managing projects, and ensuring optimal patient safety.

Posted 7/15/2026full-timeRemote • 🇵🇭 PhilippinesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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

Demonstrates expertise in clinical safety, including clinical research monitoring and pharmacovigilance, with a strong understanding of GCPs, drug development, and safety reporting. Proficient in data management and biostatistics to effectively coordinate safety data reviews and project implementation.

Highest-signal resume keywords

Clinical Safety ExperienceGCP KnowledgeDrug Development KnowledgeSafety Data TrendingBiostatistics Proficiency

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 ReviewData ManagementSAE ProcessingSafety Data CodingForecastingProblem SolvingData VisualizationProject Coordination

Soft Skills

CommunicationStakeholder ManagementCritical ThinkingCollaborationIssue Resolution

Tools & Technologies

Line ListingsVisualization Tools

Certifications & Qualifications

Bachelor’s Degree in NursingLicensed RNPhysician's Assistant

Industry Keywords

GCPsClinical TrialsSafety ReportingClinical ProceduresSafety Data Trending

About the role

Key responsibilities & impact

Coordinate and review safety data, utilizing line listings and/or other visualization tools.
Identify potential issues and resolve or escalate as appropriate.
Review safety data and provide summations for safety review meetings.
Help manage routine project implementation, forecasting and coordination.
Monitor the status of the data review and escalate any delays and/or risks to stakeholders.
Resolve complex problems through in-depth evaluation of various factors and offers solutions.

Requirements

What you’ll need

Bachelor’s degree in nursing or related Health Sciences (Physician's Assistant) or licensed RN
Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 2+ years)
2+ years clinical safety experience (clinical research monitoring, or pharmacovigilance or combination of clinical research monitoring and pharmacovigilance)
Knowledge of GCPs for medical oversight of clinical trials and SAE processing
Knowledge of drug development and safety reporting
Knowledge of safety data trending to include coding
Working knowledge of biostatistics, data management and clinical procedures

Benefits

Comp & perks

Personal protective equipment required such as protective eyewear, garments and gloves.
Regular and consistent attendance.
Global team that values passion, innovation, and a commitment to scientific excellence.
Collaborate and develop in an environment where contributions make a difference.