Clinical Trial Coordinator

Roles & Responsibilities:
• Coordinate and manage clinical trial activities according to the study protocol and regulatory requirements.
• Ensure proper documentation and maintenance of trial records, including case report forms and informed consent.
• Liaise with investigators, study participants, and internal teams to ensure smooth trial operations.
• Monitor trial progress and report any deviations or issues to the Principal Investigator.
• Assist in the preparation and submission of regulatory documents and reports.
• Support data management and ensure accuracy, completeness, and compliance of trial data.
• Participate in site visits, training sessions, and audits as required.

Qualification:
• Post Graduate degree in Science (M.Pharm, Life Sciences, Biotech, Zoology, Botany, etc.)
• PG Diploma in Clinical Research is mandatory

Experience:
• Minimum 2 years of experience in Clinical Trials
• Desirable: Experience in Clinical Research and familiarity with Telugu (reading, writing, speaking)

Skills:
• Strong organizational and coordination skills
• Knowledge of clinical trial protocols and regulatory requirements
• Effective communication and interpersonal skills
• Attention to detail and ability to maintain accurate documentation
• Ability to work independently as well as in a team environment

Walk-in Date & Venue:
Date of Walk-In: 12-02-2026
HRD Department, First Floor, Homi Bhabha Cancer Hospital Research Centre, Visakhapatnam

About the Organization:
Advanced Centre for Treatment Research and Education in Cancer (ACTREC) is a premier institute committed to cancer research, clinical care, and education, fostering innovation and excellence in oncology.

Official Notification Click Here