Clinical Research Coordinator

Role Description The Clinical Research Coordinator is a full-time, on-site role based in Bengaluru. The individual in this position will coordinate clinical research activities, including supporting the design and implementation of clinical trials and ensuring protocol adherence. Day-to-day responsibilities include managing informed consent processes, maintaining regulatory and study documentation, monitoring participant eligibility and enrollment, and scheduling study visits and follow-ups. The role also involves data collection and entry, liaising with investigators, sponsors, and ethics committees, and assisting with training learners on clinical research practices aligned with Proxima Skills Academy’s programs. The coordinator will help ensure compliance with ethical standards, quality requirements, and timelines while contributing to a professional learning environment.
Qualifications
Ability to manage informed consent processes and uphold participant rights and ethical standards (Informed Consent).
Strong understanding of study design and operational requirements, including protocol development, implementation, and compliance (Protocol).
Demonstrated skills in scientific research methods, documentation, and data quality management (Research).
Prior hands-on experience in clinical research settings, such as hospitals, CROs, or academic institutions (Clinical Research Experience).
Working knowledge of clinical trial operations, including site coordination, regulatory requirements, and safety reporting (Clinical Trials).
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, Medicine, or a related field.
Familiarity with Good Clinical Practice (GCP), ICH guidelines, and local regulatory frameworks.
Strong organizational and time-management skills, with attention to detail and accuracy.
Effective written and verbal communication skills, with the ability to collaborate with multidisciplinary teams.
Proficiency in basic computer applications, electronic data capture systems, and documentation tools.

Work arrangement
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