Senior Medical Project Coordinator
Location: Remote, India
Job Type: Full-Time
Category: Clinical Research / Pharmacovigilance
Job ID: R-01318933
Work Model: Fully Remote
About the Role
Thermo Fisher Scientific is seeking a Senior Medical Project Coordinator to support and oversee clinical trial operations across multiple programs. This role provides a unique opportunity to manage medical projects from initiation to completion, ensuring compliance, alignment, and optimal performance throughout the project lifecycle. You will collaborate closely with cross-functional teams, including clinical operations, pharmacovigilance, data management, and regulatory affairs, to ensure high-quality outcomes in global clinical trials.
Key Responsibilities
Assist in the management and ongoing evaluation of medical projects for one or more programs, ensuring consistency and compliance with internal processes.
Coordinate and review safety data using dashboards, line listings, and visualization tools; identify trends, coding issues, and necessary follow-up actions with investigator sites.
Contribute to the creation or review of safety and medical management plans, ensuring alignment with contractual obligations and service requirements.
Support project implementation, forecasting, and coordination, including monitoring metrics and budget considerations.
Monitor data review progress and escalate risks or delays to study leads and stakeholders.
Represent the project in business development, client, and investigator meetings, and participate in strategic calls as needed.
Serve as a primary point of contact for clinical/data management project teams and assist in mentoring junior staff.
Resolve complex problems using in-depth evaluation and provide actionable solutions.
Required Qualifications & Experience
Education: Bachelor’s degree in Nursing, Health Sciences, or related field (Physician’s Assistant or licensed RN preferred).
Experience: Minimum 2+ years of relevant clinical experience, including clinical research monitoring, pharmacovigilance, or a combination.
Proven ability to manage clinical trial activities, data review, and safety reporting in compliance with GCP and regulatory guidelines.
Skills & Competencies
Strong knowledge of GCPs, clinical trial safety oversight, SAE processing, and pharmacovigilance practices.
Understanding of drug development processes, safety reporting, and coding for safety data trends.
Working knowledge of biostatistics, data management, and clinical procedures.
Excellent problem-solving, critical thinking, and analytical skills.
Strong oral and written communication skills with attention to detail.
Ability to collaborate effectively in cross-functional and global teams.
Professional demeanor with the ability to perform under pressure and manage multiple priorities.
Work Environment
Standard working hours: Monday to Friday
Flexible fully remote work option
Ability to communicate effectively with diverse groups and adapt to changing priorities
Occasional travel may be required
Why Join Thermo Fisher Scientific
As a Senior Medical Project Coordinator, you will play a pivotal role in driving clinical research excellence, ensuring patient safety, regulatory compliance, and high-quality trial outcomes. Join a global leader in clinical research and make a meaningful impact on health outcomes worldwide.
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