Company Description Accelia Clinical Solutions is a specialized Site Management Organization (SMO) focused on delivering high-quality clinical trial operations with strong emphasis on compliance, precision, and integrity. The organization supports CROs and Sponsors through efficient site management, streamlined processes, and strict adherence to GCP and regulatory standards. With an extensive network of investigators, hospitals, and research professionals, Accelia provides end-to-end site support that strengthens trial quality, patient safety, and timelines.

The team values innovation, transparency, and accountability to help Sponsors achieve their research objectives confidently. Accelia is committed to turning operational challenges into effective solutions that advance science, improve healthcare, and foster long-term partnerships.

Role Description This is a full time, on-site Clinical Research Coordinator role based in the Kolkata metropolitan area.

The Clinical Research

Coordinator will support clinical trial activities, including screening and enrolling participants, scheduling study visits, and coordinating with investigators and site staff.

Responsibilities include managing informed consent processes, ensuring adherence to study protocols, maintaining accurate source documents and case report forms, and tracking study supplies and logistics. The role involves close collaboration with sponsors, CROs,



and monitors to support regulatory and ethical compliance, including GCP standards and institutional requirements. The coordinator will also assist in safety reporting, data query resolution, and maintaining organized trial documentation to ensure high-quality, timely study conduct.

Qualifications

- Demonstrated clinical research experience, including participation in clinical trials and familiarity with research workflows.
- Strong understanding of informed consent procedures and ethical requirements for human subject research.
- Ability to interpret and follow study protocols, including visit schedules, inclusion/exclusion criteria, and safety assessments.
- Knowledge of GCP guidelines and relevant regulatory frameworks governing clinical trials.
- Bachelor’s degree in life sciences, pharmacy, nursing, or a related field; advanced degree or formal clinical research training is an advantage.
- Excellent organizational, time management, and documentation skills with attention to detail.
- Effective written and verbal communication skills and ability to collaborate with multidisciplinary teams and study participants.
- Proficiency in basic computer applications and electronic data capture systems; prior experience with CTMS or EDC platforms is beneficial.
- Ability to work on-site in the Kolkata metropolitan area and manage multiple studies or tasks within defined timelines.

📌 Clinical Research Coordinator (Kolkata)
🏢 Accelia Clinical Solutions
📍 Kolkata