Job Title: Senior Medical Project Coordinator
Company: Thermo Fisher Scientific (PPD Clinical Research Services)
Location: Remote, India
Job Type: Full-Time, Fully Remote
Category: Clinical Research
Company Overview
Thermo Fisher Scientific’s Clinical Research team is part of a leading global Contract Research Organization (CRO), providing scientific and clinical expertise to develop drugs addressing challenging health concerns. The team supports clinical trials across 100+ countries, spanning laboratory, digital, and decentralized trial services.
Work Schedule
Monday – Friday (Standard office hours)
Fully remote work environment
Job Summary
The Senior Medical Project Coordinator assists in managing and evaluating medical projects across clinical trials. This includes oversight of clinical safety data, pharmacovigilance activities, regulatory compliance, and coordination across study teams to ensure optimal project performance.
Key Responsibilities
Assist in management and ongoing evaluation of medical projects to ensure alignment, consistency, and compliance of internal processes.
Coordinate and review safety data using line listings, dashboards, and visualization tools.
Identify safety trends, coding inconsistencies, and potential follow-ups with investigator sites.
Provide summations for safety review meetings and review designated sections of aggregate reports.
Assist in creating/reviewing safety and medical management plans for studies.
Manage routine project implementation, including forecasting, coordination, metrics, and budget considerations.
Monitor data review status and escalate delays or risks to stakeholders.
Present at business development, client, and investigator meetings.
Serve as a point of contact for clinical/data management project teams.
Assist in training and mentoring team members.
Resolve complex problems through in-depth evaluation and propose solutions.
Education & Qualifications
Bachelor’s degree in Nursing, Health Sciences, or Physician Assistant program. Licensed RN preferred.
Experience:
2+ years in clinical safety, clinical research monitoring, or pharmacovigilance (or combination).
Knowledge & Skills:
Good Clinical Practices (GCP) for medical oversight and SAE processing.
Understanding of drug development and safety reporting.
Experience in safety data trending and coding.
Working knowledge of biostatistics, data management, and clinical procedures.
Strong problem-solving, critical thinking, and attention to detail.
Effective oral and written communication skills.
Ability to work collaboratively in a team and maintain professionalism under pressure.
Work Environment
Fully remote office setup; ability to communicate and collaborate with diverse groups.
Ability to work upright and stationary during typical working hours.
Proficiency with standard office equipment and technology.
Ability to handle multiple projects under pressure and prioritize tasks effectively.
Travel may be required (as per recruiter guidance).
Andra Pradesh :
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Dunboyne |Republic of Ireland :
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Donegal |China :
China | Quarry Bay |Hubei :
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Hangzhou |Melbourne :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |Buenos Aires :
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Zaventem |Bosnia and Herzegovina :
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Riyadh | Najran | Jeddah | King Abdullah Economic City | Rabigh | Khulais |Nišava District :
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