Senior Medical Project Coordinator – Remote, India
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 join our global Clinical Research Services team. As part of our leading Contract Research Organization (CRO), you will play a key role in supporting the management and oversight of clinical trials across all phases of drug development. This position offers the opportunity to contribute to life-changing therapies, ensuring high standards of safety, accuracy, and compliance in clinical research.
The ideal candidate will have strong clinical safety and project management experience, with a background in pharmacovigilance or clinical research monitoring.
Key Responsibilities
Coordinate and review safety data, using dashboards, line listings, and visualization tools to identify trends, coding inconsistencies, and potential issues.
Support preparation of safety summaries for review meetings and designated sections of aggregate reports.
Assist in the creation and review of medical management and safety plans, ensuring alignment with contracts and study requirements.
Manage routine project implementation, forecasting, and coordination, including review of metrics, timelines, and budgets.
Monitor project progress and escalate risks or delays to study leads and stakeholders.
Serve as the primary contact for clinical or data management project teams, providing guidance and resolving complex project issues.
Present at client, investigator, and business development meetings as needed.
Assist management in training and mentoring junior team members.
Required Experience & Qualifications
Bachelor’s degree in Nursing, Health Sciences, or related field (Physician’s Assistant) or licensed RN.
Minimum 2+ years of clinical safety experience, including clinical research monitoring, pharmacovigilance, or a combination of both.
Knowledge of Good Clinical Practice (GCP) and medical oversight of clinical trials.
Understanding of drug development, safety reporting, and data trending (including coding).
Familiarity with biostatistics, clinical procedures, and data management.
Strong problem-solving, critical thinking, and attention to detail.
Excellent oral and written communication skills with the ability to work effectively in a collaborative, cross-functional team environment.
Preferred Qualifications
Prior experience with global clinical trial oversight and safety management.
Experience in regulatory submissions, safety reports, or aggregate safety reviews.
Ability to mentor junior staff and contribute to process improvements.
Work Environment
Fully remote work environment with occasional travel as required.
Must be able to communicate effectively with diverse teams globally.
Ability to manage multiple priorities under pressure while maintaining high-quality standards.
Proficiency in standard office technology and clinical trial systems.
Why Thermo Fisher Scientific?
Join a global organization dedicated to enabling healthier, cleaner, and safer communities. Our teams are empowered to drive innovation in clinical research, development, and delivery of life-changing therapies. We provide resources for professional growth and encourage collaboration across disciplines, creating opportunities to make a global impact.
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