Clinical Research Coordinator intern

Location: Vasanthanagar

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
About the Role 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.

Key Responsibilities  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.
Skills Required  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.
Educational Qualification 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
What You Will Learn  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
Career Growth Successful interns can build their career toward roles such as:
Clinical Research Coordinator → Clinical Research Associate → Senior CRA → Clinical Trial Manager → Clinical Project Manager
Ideal Candidate 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!