Clinical Research Coordinator intern

Proxima Skills Academy · Bengaluru, India

Position: Clinical Research Coordinator Intern

Experience: Fresher / 0–1 Year

Employment Type: Internship

Department: Clinical Research

Eligibility: Life Sciences / Pharmacy / Medical / Allied Health Sciences Graduates

We are looking for enthusiastic and detail-oriented Clinical Research Coordinator Interns who are interested in building a career in clinical research. The selected candidates will receive practical exposure to clinical trial coordination, documentation, regulatory requirements, and clinical research processes.

• Assist Clinical Research Coordinators in day-to-day clinical trial activities.
• Support patient visit scheduling and trial-related coordination.
• Maintain and organize clinical trial documents and study files.
• Assist with Case Report Form (CRF/eCRF) data collection and documentation.
• Support data entry and verification of clinical trial information.
• Assist in maintaining Trial Master File (TMF) and Investigator Site File (ISF) documentation.
• Follow study protocols, SOPs, GCP guidelines, and regulatory requirements.
• Coordinate with investigators, study teams, patients, and other clinical research personnel.
• Assist with preparation of study-related reports and records.
• Support monitoring visits, audit preparation, and regulatory documentation when required.
• Maintain confidentiality and ensure accuracy of clinical research data.

• Good communication and interpersonal skills.
• Basic understanding of clinical research concepts.
• Good documentation and organizational skills.
• Attention to detail and accuracy.
• Basic knowledge of MS Word and MS Excel.
• Ability to work effectively in a team.
• Willingness to learn clinical trial processes and regulatory requirements.

Candidates from the following backgrounds can apply:

• B.Pharm / M.Pharm
• Pharm.D
• MBBS / BDS / BHMS / BAMS
• B.Sc / M.Sc – Life Sciences
• Biotechnology
• Microbiology
• Biochemistry
• Nursing
• Allied Health Sciences
• Other relevant healthcare or life-science backgrounds

• Clinical Trial Lifecycle
• Good Clinical Practice (GCP)
• Clinical Trial Documentation
• CRF / eCRF
• Informed Consent Process
• Trial Master File (TMF)
• Investigator Site File (ISF)
• Protocol & SOP Compliance
• Patient/Subject Coordination
• Safety Reporting Basics
• Regulatory & Ethics Committee Processes
• Clinical Data Management Basics

Successful interns can build their career toward roles such as:

Clinical Research Coordinator → Clinical Research Associate → Senior CRA → Clinical Trial Manager → Clinical Project Manager

Fresh graduates who are passionate about clinical research, clinical trials, healthcare, and pharmaceutical research and want practical industry exposure are encouraged to apply.

• Freshers are welcome!