Job Title: Senior Medical Project Coordinator
Location: Remote – India
Job ID: R-01318933
Employment Type: Full-Time
Category: Clinical Research
Work Mode: Fully Remote
Work Schedule: Standard (Monday to Friday)
About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in serving science, dedicated to making the world healthier, cleaner, and safer. Our Clinical Research team powers the PPD® clinical research portfolio and supports drug development through clinical trials in 100+ countries. Our teams work across laboratory, digital, and decentralized clinical trial services to deliver life-changing therapies.
Role Overview
The Senior Medical Project Coordinator supports the management and ongoing evaluation of medical projects across one or more programs. You will collaborate with management and stakeholders to ensure alignment, consistency, and compliance of internal processes, optimizing project performance and resolving issues throughout the project lifecycle.
Key Responsibilities
Assist in managing and evaluating medical projects to ensure consistency, alignment, and compliance with internal processes.
Coordinate and review safety data using line listings, dashboards, and visualization tools.
Identify safety trends, coding inconsistencies, and potential issues for follow-up or escalation.
Summarize safety data for review meetings and assist in reviewing designated sections of aggregate reports.
Support creation and review of safety and medical management plans ensuring alignment with contracts and services.
Manage routine project implementation tasks including forecasting, coordination, metrics review, and budget considerations.
Monitor data review status and escalate delays or risks to stakeholders including study leads.
Present at business development, client, and investigator meetings; participate in strategy and business development calls.
Resolve complex problems through detailed evaluation and propose solutions.
Serve as the primary point of contact for clinical/data management project teams.
Assist in training and mentoring team members as needed.
Qualifications
Education
Bachelor’s degree in Nursing, related Health Sciences (e.g., Physician Assistant), or licensed Registered Nurse (RN).
Experience
Minimum of 2+ years clinical safety experience (clinical research monitoring, pharmacovigilance, or a combination).
Knowledge of Good Clinical Practices (GCP) related to medical oversight and serious adverse event (SAE) processing.
Understanding of drug development and safety reporting processes.
Familiarity with safety data trending and coding.
Working knowledge of biostatistics, data management, and clinical procedures.
Skills & Abilities
Strong problem-solving and critical thinking skills.
Effective oral and written communication abilities.
High attention to detail.
Ability to work collaboratively in a team environment.
Maintain a positive and professional demeanor under challenging circumstances.
Ability to manage multiple priorities and work effectively under pressure.
Willingness and ability to travel as required.
Work Environment
Ability to communicate clearly and understand diverse perspectives.
Capable of working upright and stationary during typical working hours.
Proficient in using standard office equipment and technology.
Thermo Fisher Scientific supports employee health and well-being and fosters a balanced work environment.
Equal Opportunity & Accessibility
Thermo Fisher Scientific is an Equal Opportunity Employer and is committed to providing reasonable accommodations for individuals with disabilities throughout the application and employment process. Please contact us to request accommodations.
Learn More & Apply
For more information, visit: www.thermofisher.com
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