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Sr Medical Project Coordinator

2+ years
Not Disclosed
10 Sept. 26, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Sr. Medical Project Coordinator

Location: Remote, India
Job ID: R-01318933
Job Type: Full-time
Category: Clinical Research
Work Schedule: Standard (Mon–Fri)


Company Overview

Thermo Fisher Scientific is a global leader in life sciences, enabling customers to make the world healthier, cleaner, and safer. Through its PPD® clinical research portfolio, the organization delivers laboratory, digital, and decentralized clinical trial services across 100+ countries.

Employees contribute to meaningful work spanning research, development, and delivery of life-changing therapies, ensuring quality, accuracy, and compliance in clinical trials.


Job Summary

Supports the management and evaluation of medical projects within clinical research programs. Ensures alignment, consistency, compliance with internal processes, and optimal performance throughout the project lifecycle. Acts as a key point of contact for clinical/data management project teams and may assist with training or mentoring.


Key Responsibilities

Medical Project Oversight:

  • Assist in management and ongoing evaluation of medical projects for one or more programs.

  • Ensure consistency, alignment, and compliance of internal processes.

  • Support optimal performance and resolution of issues throughout project lifecycle.

Safety Data Management:

  • Coordinate and review safety data using line listings, dashboards, or other visualization tools.

  • Identify safety trends, coding inconsistencies, and follow-up actions with investigator sites.

  • Review safety data for designated sections of aggregate reports.

  • Provide summations for safety review meetings.

Project Planning & Implementation:

  • Help create or review safety and medical management plans.

  • Manage routine project implementation, forecasting, and coordination, including review of metrics and budget considerations.

  • Monitor status of data review and escalate delays or risks to stakeholders.

  • Participate in strategy/business development meetings as needed.

Problem Solving & Leadership:

  • Resolve complex problems through in-depth evaluation and provide solutions.

  • Serve as primary contact for project teams and support management in training and mentoring.


Qualifications

Education:

  • Bachelor’s degree in Nursing, related Health Sciences, or licensed RN/Physician’s Assistant.

Experience:

  • Minimum 2+ years clinical safety experience (clinical research monitoring, pharmacovigilance, or a combination).

  • Previous experience providing knowledge, skills, and abilities to perform the role effectively.

Knowledge, Skills, and Abilities:

  • Knowledge of GCPs for medical oversight of clinical trials and SAE processing.

  • Understanding of drug development and safety reporting.

  • Experience with safety data trending and coding.

  • Working knowledge of biostatistics, data management, and clinical procedures.

  • Strong problem-solving and critical-thinking skills.

  • Excellent oral and written communication skills.

  • High attention to detail and accuracy.

  • Ability to work collaboratively in a team environment.

  • Professional demeanor in challenging circumstances.


Work Environment & Requirements

  • Ability to communicate effectively with diverse groups.

  • Ability to work upright and stationary for standard working hours.

  • Proficiency in standard office equipment and technology.

  • Ability to prioritize multiple projects and perform under pressure.

  • May require travel (details provided by recruiter).


Impact & Contribution

  • Ensures safe, compliant, and efficient management of medical projects.

  • Supports clinical research teams in data review, issue resolution, and project oversight.

  • Contributes to quality and integrity of clinical trials while fostering team collaboration.