Clinical Research Associate
Proxima Skills Academy
About the Role
This is a full-time, on-site position based in Kolkata. The role involves supporting the planning, implementation, and monitoring of clinical trials according to approved protocols and regulatory requirements.
Key Responsibilities
- Coordinate with clinical sites.
- Assist in study start-up activities.
- Ensure accurate data collection and documentation.
- Track study progress.
- Review case report forms.
- Support site training on study procedures.
- Help maintain compliance with ethical guidelines and standard operating procedures.
- Collaborate with clinical operations teams, investigators, and other stakeholders.
- Contribute to learner training and mentoring where relevant.
Requirements & Tech Stack
- Clinical trial Protocol development, interpretation, and adherence.
- Skills related to the Clinical Research Associate function, including site communication, monitoring support, and documentation management.
- Experience or understanding of Clinical Trials, including study phases, regulatory requirements, and ethical guidelines.
- Research skills, such as data review, analysis basics, literature search, and report preparation.
- Familiarity with Clinical Operations, including study coordination, site management, and SOP-driven processes.
- Knowledge of Good Clinical Practice (GCP) and applicable regulatory standards.
Qualifications
- Relevant degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field.
- Strong attention to detail.
- Organizational skills.
- Ability to manage multiple tasks and timelines.
- Effective written and verbal communication skills.
- Ability to work collaboratively with multidisciplinary teams.
- Prior internship or experience in clinical research or healthcare settings is an advantage.






