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Sr Medical Project Coordinator

Thermo Fisher Scientific
Thermo Fisher Scientific
1-2 years
Not Disclosed
10 Dec. 15, 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

Senior Medical Project Coordinator

Location: Remote, India
Job ID: R-01318933
Employment Type: Full-Time
Category: Clinical Research | Pharmacovigilance | Medical Project Management


About the Role

Thermo Fisher Scientific is seeking a Senior Medical Project Coordinator to oversee medical and safety-related aspects of clinical trials from initiation to completion. This role provides an opportunity to work on global clinical programs, collaborating with cross-functional teams to ensure data integrity, compliance, and operational excellence.

As a Senior Medical Project Coordinator, you will manage, review, and evaluate safety data, monitor study deliverables, and support medical project planning. This position offers exposure to all stages of drug development, from early-phase trials to post-marketing activities, while contributing to the safety and efficacy evaluation of investigational products.


Key Responsibilities

Medical Project Oversight

  • Coordinate and review safety data using line listings, dashboards, and visualization tools to identify trends, coding consistencies, and potential site follow-ups.

  • Assist in preparing data summaries for safety review meetings and designated sections of aggregate safety reports.

  • Support the development and review of Safety and Medical Management Plans, ensuring alignment with contracts and study requirements.

  • Monitor project implementation, timelines, metrics, and budgets, escalating risks or delays to stakeholders promptly.

  • Serve as a primary point of contact for clinical and data management project teams, supporting effective communication across functions.

Collaboration & Communication

  • Present updates and findings in business development, client, and investigator meetings.

  • Contribute to strategy and business development calls as needed.

  • Assist in training and mentoring junior staff or project team members.

Problem Solving & Quality Assurance

  • Resolve complex project and safety data issues through in-depth evaluation and critical thinking.

  • Ensure adherence to global regulatory standards, GCP guidelines, and internal SOPs for safety data management and medical oversight.

  • Apply knowledge of clinical trial processes, drug development, and safety reporting to support high-quality deliverables.


Education & Experience Requirements

  • Bachelor’s degree in Nursing, Health Sciences, or related field (Physician’s Assistant or licensed RN preferred).

  • Minimum 2+ years of clinical safety experience, including pharmacovigilance, clinical research monitoring, or a combination of both.

  • Previous experience in clinical trials or pharmacovigilance providing knowledge of safety data management, SAE reporting, and clinical oversight.


Required Skills & Competencies

  • Strong understanding of GCPs, drug development, and safety reporting.

  • Experience in safety data trending, coding, and basic biostatistics.

  • Working knowledge of clinical procedures and data management systems.

  • Excellent problem-solving, critical thinking, and analytical skills.

  • Strong oral and written communication skills, with attention to detail.

  • Ability to work collaboratively in a cross-functional team environment.

  • Professional demeanor with the ability to manage multiple tasks under pressure.


Work Environment

  • Fully remote, with potential travel as required.

  • Standard office environment with typical working hours.

  • Proficiency with office equipment and digital communication tools required.

  • Ability to manage multiple priorities and maintain productivity under pressure.