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Senior Medical Project Coordinator
Thermo Fisher ScientificManage and evaluate medical projects for Thermo Fisher Scientific in EMEA. Oversee project implementation, coordination, and compliance in clinical research.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical safety, project management, and medical oversight of clinical trials, with a strong focus on safety data analysis and regulatory compliance. Proven ability to lead teams, mentor staff, and manage complex clinical projects effectively.
Highest-signal resume keywords
Clinical Safety ExperienceProject Management SkillsAdvanced Knowledge of GCPsSafety Data TrendingMentoring and Training Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Research MonitoringPharmacovigilanceSafety Data AnalysisBiostatisticsData ManagementClinical ProceduresBudget ManagementMedical Management PlansProblem SolvingCoding Consistencies
Soft Skills
Attention to DetailEffective CommunicationCollaborationLeadership
Certifications & Qualifications
Bachelor's Degree in NursingLicensed RNPhysician's Assistant
Industry Keywords
GCPsDrug DevelopmentSafety ReportingClinical TrialsMedical Monitoring Services
About the role
Key responsibilities & impact- Manages, coordinates and evaluates medical projects for one or more programs
- Represents the company in the medical research community and develops collaborative relationships with client company personnel
- Works independently to perform first pass review of safety data
- Reviews data for safety trends, coding consistencies, and potential follow up with investigator sites
- Proactively identifies any potential issues and resolves or escalates as appropriate
- Independently functions as the Project Lead for medical monitoring services
- Manages project implementation, coordination, maintenance and close out of assigned studies as applicable
- Serves as the primary point of contact for clinical project teams on studies
- Creates and maintains medical management plan(s) on studies
- Independently determines hours required for out of scope work for the teams
- Attends meetings to discuss/justify the modification requirements
- Resolves complex problems through in-depth evaluation of various factors and offers solutions
Requirements
What you’ll need- Bachelors 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 project management and budget skills
- Effective mentoring skills and ability to train and lead others
- Strong attention to detail
Benefits
Comp & perks- Health insurance
- Professional development opportunities
- Flexible working hours