Clinical Research Intern

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Skills you'll use

What you'll do

• Work on supporting trial monitoring, documentation and regulatory submissions alongside the core team
• Apply Good Clinical Practice (GCP), Clinical Trial Auditing, Regulatory Submission (CDSCO), Case Report Form (CRF) Review to live, production-facing problems
• Document your work clearly for reviewers and stakeholders
• Participate in reviews and act on the feedback you receive
• Collaborate across engineering, product, design or business as required
• Follow the team's quality, testing and documentation standards

Who can apply

• Pursuing or recently completed B.Pharm/M.Pharm, B.Sc/M.Sc (Life Sciences), BDS, MBBS or PG Diploma in Clinical Research
• Graduating batch 2025, 2026 or 2027 — final-year students and recent graduates welcome
• 60% / 6.0 CGPA and above preferred; strong project work is considered alongside academics
• Working knowledge of Good Clinical Practice (GCP), Clinical Trial Auditing, Regulatory Submission (CDSCO) (or a genuine willingness to learn them)
• Exposure to Case Report Form (CRF) Review, Informed Consent Process, Source Data Verification is an advantage
• Clear written and verbal communication in English, and care with detail in your work
• No prior work experience required — this is a fresher-friendly internship
• Based in Bengaluru, Karnataka or willing to work from there for the internship period

Perks & benefits

Interview & selection process

4 rounds — typical selection flow for this role:

1. 1Application screening & resume shortlisting by the talent team
2. 2Technical interview on fundamentals and your projects
3. 3Practical assignment or case study with a short walkthrough
4. 4HR discussion — stipend, start date, expectations and offer

About F22 Labs

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