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Clinical Trial Coordinator – Remote (India)

0-1 years
upto 5 LPA
20 Nov. 18, 2025
Job Description
Job Type: Full Time 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

Clinical Trial Coordinator – Remote (India)


Freshers Eligible | Full-Time | R-01329479

About the Role
Thermo Fisher Scientific is hiring a Clinical Trial Coordinator to support global clinical research operations within the PPD® clinical research services division. This role offers a fully remote work environment and an opportunity to begin a career in clinical research with one of the world’s leading contract research organizations (CROs).

You will contribute to clinical trials across pharmaceutical, biotech, commercial, and government projects—ensuring operational accuracy, supporting study start-up activities, and maintaining essential documentation throughout the trial lifecycle.

Work Schedule
Standard, Monday to Friday

Location
Remote, India


Key Responsibilities

  • Provide administrative and technical support to clinical project teams.

  • Maintain audit-ready documentation in alignment with SOPs and project timelines.

  • Support site activation processes and contribute to developing activation pathways.

  • Collaborate with investigators and site personnel during feasibility assessments.

  • Build knowledge of local clinical trial sites and contribute to site selection activities.

  • Assist with onboarding and training of new team members.

  • Participate in departmental initiatives aimed at quality and process improvement.

  • Represent the organization within the global clinical research community.


Qualifications

Education:
Bachelor’s degree preferred.

Experience:
Freshers can apply.
(Previous clinical research exposure is beneficial but not mandatory for fresher applicants.)

  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years).

  • In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.


Skills and Competencies

  • Strong attention to detail and ability to manage multiple tasks.

  • Capable of working both independently and within cross-functional teams.

  • Good analytical understanding of project-related data and systems.

  • Ability to adapt to shifting priorities and support rapidly changing project needs.

  • Basic understanding or willingness to learn ICH-GCP guidelines and regulatory requirements.

  • Excellent communication and interpersonal skills.

  • Proficiency in MS Office; willingness to learn clinical trial management systems.

  • Ability to successfully complete internal training programs.


Work Environment

Thermo Fisher Scientific promotes a balanced, healthy work culture. The role requires:

  • Clear communication with diverse stakeholders.

  • Ability to work in a stationary position for extended hours.

  • Comfort with standard office tools and remote-working technology.

  • Strong prioritization skills under pressure.

  • Occasional travel, depending on project requirements.