Job Title:
Senior Medical Project Coordinator
Location:
Remote, India
Job ID:
R-01318933
Job Type:
Full-time
Category:
Clinical Research / Pharmacovigilance
Work Schedule:
Standard (Mon-Fri)
Work Environment:
Office-based (Remote work)
May require travel
Able to communicate and collaborate effectively with diverse groups
Proficient in standard office equipment and technology
Able to perform under pressure and manage multiple projects simultaneously
About the Role:
The Senior Medical Project Coordinator is responsible for managing and evaluating medical projects across one or more programs. This includes oversight of safety data, ensuring internal process compliance, supporting issue resolution, and optimizing project performance throughout the project lifecycle.
Key Responsibilities:
Safety Data & Medical Oversight:
Coordinate and review safety data using line listings, dashboards, and visualization tools.
Identify trends, coding consistencies, and potential follow-up actions with investigator sites.
Summarize safety data for review meetings.
Assist in creating/reviewing safety and medical management plans.
Project Coordination & Management:
Monitor project implementation, forecasting, and coordination, including metrics and budget considerations.
Track status of data review and escalate delays or risks to stakeholders.
Serve as primary point of contact for clinical/data management project teams.
Participate in business development, client, and investigator meetings.
Resolve complex project issues by evaluating multiple factors and proposing solutions.
Training & Mentorship:
Assist management in training and mentoring team members as needed.
Qualifications & Experience:
Education:
Bachelor’s degree in Nursing, Health Sciences, or related field (Physician’s Assistant or RN).
Experience:
2+ years of clinical safety experience in clinical research monitoring, pharmacovigilance, or a combination.
Experience in safety data trending, coding, and regulatory compliance.
Knowledge, Skills & Abilities:
Knowledge of GCP and SAE processing for clinical trials.
Understanding of drug development and safety reporting.
Working knowledge of biostatistics, data management, and clinical procedures.
Strong problem-solving and critical thinking skills.
Excellent oral and written communication skills.
Attention to detail and ability to work collaboratively in a team environment.
Ability to maintain professionalism under challenging circumstances.
About the Company:
Thermo Fisher Scientific is a global leader in clinical research services, supporting drug development in over 100 countries. Their clinical research portfolio includes laboratory, digital, and decentralized trial services to improve global health outcomes.
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Japan | Saitama |Tokyo :
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