Clinical Trial Coordinator
Location: Remote, India
Job ID: R-01329479
Job Type: Full-time
Category: Clinical Research
Work Schedule: Standard (Mon–Fri)
Work Environment: Office (Fully Remote)
About the Role
At Thermo Fisher Scientific, you’ll engage in meaningful work that makes a global impact. As part of the PPD® Clinical Research Services team within our Clinical Operations, you will support the entire clinical trial process—from study start-up and monitoring to close-out—across both commercial and government projects. Together, we help clients accelerate drug development, minimize delays, and execute cost-efficient, high-quality clinical studies.
Key Responsibilities
Provide administrative and technical support to the Project Team.
Ensure audit readiness by reviewing files according to organizational SOPs and departmental guidance.
Support site activation activities and assist in developing the critical path for rapid site activation in assigned projects.
Represent the organization within the global medical research community.
Develop collaborative relationships with investigators and site personnel to conduct feasibility assessments within defined timelines.
Build and maintain a local knowledge base of clinical sites to support feasibility and site selection activities.
Use local knowledge and internal/external site lists to contribute to the site tiering process and align with sponsor needs.
Act as a buddy/mentor during the onboarding phase for new staff.
Support training initiatives and participate in process improvement or departmental enhancement projects.
Education & Experience
Bachelor’s degree preferred.
Minimum 2 years of relevant experience in clinical research or related fields.
Equivalent combinations of education, training, and relevant experience may be considered.
Knowledge, Skills & Abilities
Ability to work independently or within a team as required.
Strong organizational skills and attention to detail.
Proven ability to manage multiple tasks and priorities efficiently.
Skilled in analyzing project-specific data/systems for accuracy and performance.
Adaptable and flexible in response to changing project timelines and priorities.
Working knowledge of ICH-GCP, country regulations, and company/Client SOPs/WPDs for non-clinical and clinical operations.
Excellent communication and interpersonal skills.
Proficient in MS Office (Word, Excel, PowerPoint) and capable of mastering clinical trial database systems.
Ability to successfully complete the PPD Clinical Training Program.
Working Environment
Thermo Fisher Scientific values the health and wellbeing of all employees, fostering a balanced environment where individuals can thrive.
Requirements:
Strong verbal and written communication skills to interact effectively with diverse teams.
Ability to remain stationary for standard working hours.
Proficiency in standard office technology and software tools.
Capable of performing under pressure, managing multiple projects simultaneously.
Travel may be required (details to be provided by the recruiter).
Why Join Us
At Thermo Fisher Scientific, you’ll be part of a team that’s advancing global health, driving innovation, and supporting patients worldwide.
Watch our colleagues share the Top 5 Reasons to Work With Us.
Equal Employment Opportunity
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.
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Birmingham |Alaska :
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China | Quarry Bay |Hubei :
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