Clinical Research Coordinator

Proxima Skills Academy; India; On-site; INR 250,000 - 420,000; Full time

Job summary

Proxima Skills Academy in India is seeking a Clinical Research Coordinator for a full-time role to coordinate screening, enrollment, follow-up, and data entry in line with study protocols.

The position requires adherence to regulatory and ethical guidelines, informed consent, site readiness, and collaboration with investigators, sponsors, and monitors. Freshers are eligible, with a background in Life Sciences or related field; knowledge of GCP and basic computer/EDC tools is preferred.

Qualifications

• Freshers are eligible to apply.
• Knowledge of GCP, ethics and regulatory requirements in clinical research.
• Strong attention to detail, organizational skills, and ability to manage multiple tasks and timelines.
• Effective written and verbal communication, collaborative in multidisciplinary teams.
• Proficiency in basic computer applications and electronic data capture systems.

Responsibilities

• Coordinate and manage clinical research activities, including participant screening, enrollment, and follow-up.
• Obtain informed consent and maintain accurate study documentation.
• Schedule study visits and collect/enter data, supporting investigators and research staff.
• Communicate with sponsors or monitors and assist with site readiness and supply management.

Skills

clinical research operations

Research & Clinical Research

Education

Life sciences / related field degree

Tools

EDC systems

Job description

Role Description The Clinical Research Coordinator role is a full-time role. This role involves coordinating and managing clinical research activities, including participant screening, enrollment, and follow-up in accordance with approved study protocols. The Clinical Research Coordinator will obtain informed consent, maintain accurate and timely study documentation, and ensure adherence to regulatory and ethical guidelines. Responsibilities include scheduling study visits, collecting and entering data, supporting investigators and research staff, and communicating with sponsors or monitors as required. The role also includes assisting with site readiness, maintaining study supplies, and contributing to continuous improvement of clinical research processes within the academy’s training and project ecosystem.

Qualifications

• Only Freshers are eligible to apply.
• Candidates should possess skills in clinical research operations, including Research and Clinical Research Experience.
• Candidates should possess skills in study design and conduct, including Protocol and Clinical Trials.
• Candidates should possess skills related to participant engagement and ethics, including Informed Consent.
• Relevant educational background in Life Sciences, Pharmacy, Nursing, Medicine, or related field (Bachelor’s or Master’s degree preferred).
• Knowledge of Good Clinical Practice (GCP), ethical guidelines, and regulatory requirements in clinical research.
• Strong attention to detail, organizational skills, and ability to manage multiple tasks and timelines.
• Effective written and verbal communication skills, with the ability to work collaboratively in multidisciplinary teams.
• Proficiency in basic computer applications and electronic data capture systems; prior exposure to clinical research documentation is an advantage.