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Clinical Trial Coordinator (Level I)

Thermo Fisher Scientific
Thermo Fisher Scientific
Fresher years
3-5 LPA
Remote, India, India
20 April 23, 2026
Job Description
Job Type: Remote Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. 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

Clinical Trial Coordinator (Level I) – Entry Level

Location: Remote, India
Job Type: Full-Time
Category: Clinical Research
Work Model: 100% Remote
Experience Required: 0–2 Years (Freshers Eligible)


About the Organization

This opportunity is part of a globally recognized Clinical Research Organization supporting large-scale drug development programs across pharmaceutical and biotechnology companies. The clinical research division operates at the forefront of innovation, contributing to thousands of clinical trials across more than 100 countries.


Job Overview

The Clinical Trial Coordinator (Level I) is an entry-level role designed for candidates looking to build a career in clinical research. This position focuses on trial coordination, documentation management, and operational support across global clinical studies. You will work closely with cross-functional teams to ensure trials are executed efficiently, compliantly, and within timelines.


Key Responsibilities

  • Coordinate and execute assigned clinical trial activities as per study task matrix

  • Perform internal, departmental, country-level, and investigator file reviews with proper documentation

  • Ensure all assigned tasks are completed within timelines, budget, and quality expectations

  • Maintain and manage study documentation including study team lists, training trackers, and access logs

  • Support Trial Master File ((e)TMF) maintenance and ensure audit readiness

  • Provide operational support for clinical systems such as CTMS, eTMF, and study activation platforms

  • Handle administrative responsibilities including document processing, communications, and reporting

  • Assist in organizing internal and client meetings, including preparation of meeting minutes

  • Analyze study metrics and support resolution of documentation-related discrepancies

  • Maintain vendor trackers and support site-level documentation activities

  • Assist in preparation and distribution of Investigator Site Files (ISF) and study-related materials


Educational Qualification

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field


Experience Requirement

  • 0–2 years of experience in clinical research or related domain

  • Freshers with strong foundational knowledge of clinical trials and GCP are encouraged to apply


Required Skills and Competencies

  • Strong organizational and multitasking abilities with high attention to detail

  • Basic understanding of clinical trial processes and regulatory guidelines (ICH-GCP)

  • Proficiency in Microsoft Office tools (Word, Excel, PowerPoint)

  • Ability to work independently as well as in a collaborative team environment

  • Strong analytical and problem-solving skills

  • Effective communication and interpersonal skills

  • Adaptability to dynamic project timelines and priorities

  • Willingness to learn clinical trial systems and tools


Work Environment

  • Remote/home office setup

  • Standard working schedule (Monday to Friday)

  • Exposure to global clinical research operations and digital systems


Why This Role Matters

This position offers a strong entry point into the global clinical research industry, providing hands-on exposure to trial coordination, documentation systems, and cross-functional collaboration. It is particularly suited for candidates aiming to transition into roles such as Clinical Research Associate (CRA), Clinical Project Coordinator, or Clinical Operations Specialist.


How to Apply

Apply through the official careers portal or trusted job platforms. For more verified global clinical research and pharmacovigilance opportunities, visit ThePharmaDaily.com