In the ever-evolving world of clinical research, Clinical Trial Coordinators (CTCs) are the unsung heroes ensuring that life-changing treatments reach the market — safely, efficiently, and ethically. At Thermo Fisher Scientific, a global leader in science and innovation, this role is more than just administrative; it’s a gateway to making a meaningful impact on global health.

Clinical Trial Coordinator

Location  Remote, India  Job Id  R-013294

Why This Role Matters

Thermo Fisher Scientific’s clinical research services, under the PPD® umbrella, support drug development across commercial and government sectors. From early feasibility to study closeout, Clinical Trial Coordinators play a crucial part in every stage — ensuring that trials are audit-ready, documents are meticulously managed, and site activation progresses without unnecessary delays.

In other words, they keep clinical operations running smoothly behind the scenes.

What Does a Clinical Trial Coordinator Do?

The CTC role is a blend of project support, documentation management, and regulatory compliance. Here’s a breakdown of their core contributions:

Audit Readiness: Ensuring all essential files are reviewed in accordance with standard operating procedures (SOPs).

Site Activation Support: Assisting with the development of a critical path to accelerate study start-up timelines.

Feasibility & Relationship Building: In some cases, CTCs work directly with sites and investigators to assess feasibility and build a knowledge base of site capabilities.

Process Improvement: From onboarding new team members to participating in departmental initiatives, CTCs often contribute to enhancing operational efficiency.

System & Document Management: They maintain data integrity across multiple platforms and ensure compliance with global regulations such as ICH-GCP.

Who Thrives in This Role?

The ideal Clinical Trial Coordinator is not just organized — they are detail-oriented, adaptable, and proactive. This role suits professionals who:

Excel in multitasking and time management

Are familiar with clinical documentation, regulatory environments, or healthcare operations

Communicate clearly with both internal teams and external stakeholders

Are comfortable using clinical trial management systems (CTMS) and tools like Microsoft Office

Embrace change and work efficiently under pressure.

What Are the Qualifications?

While a Bachelor’s degree is preferred, what truly counts is experience. At least two years in clinical research, healthcare administration, or a related field can be sufficient. Thermo Fisher also recognizes that skill and potential can come from various paths — a strong mix of education, training, and practical experience is valued.

Remote but Connected

This role is fully remote in India, but don’t mistake “remote” for disconnected. Clinical Trial Coordinators collaborate with global teams, investigators, and stakeholders across regions. While some travel may be required, most interactions happen through robust digital systems and communication platforms.

Why Choose Thermo Fisher Scientific?

At Thermo Fisher, the work is driven by purpose. As a Clinical Trial Coordinator, you’re contributing to something larger than yourself — accelerating the development of treatments that could save lives or dramatically improve patient outcomes.

You’ll also join a company that values employee well-being, professional development, and diversity of thought. The culture encourages learning, growth, and continuous improvement — both at the personal and organizational level.

Becoming a Clinical Trial Coordinator at Thermo Fisher Scientific is more than a job — it’s an opportunity to be part of a global mission to improve healthcare. Whether you’re a seasoned clinical research professional or someone looking to transition into this impactful field, this role offers a platform to contribute meaningfully and grow professionally.

Looking to make a difference? This just might be your next step.

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