Trainee – Clinical Development & Medical Affairs

BANGALORE (IN)ONSITEPOSTED: 7/2/2026
PHARMAFull-time
HIRING ORGANIZATIONIMMUNEEL THERAPEUTICS PVT. LTD.Technology
Immuneel Therapeutics Pvt. Ltd.

ROLE DEFINITION & RESPONSIBILITIES

Immuneel Therapeutics Pvt. Ltd. has announced an excellent career opportunity for M.Pharm and Pharm.D freshers looking to begin their careers in Clinical Operations, Pharmacovigilance, Drug Safety, and Medical Affairs. The company is hiring for the position of Trainee – Clinical Development & Medical Affairs at its Bengaluru office.

Key Responsibilities

Supporting Clinical Development projects
Assisting in Pharmacovigilance activities
Drug Safety monitoring and documentation
Adverse Event (AE) reporting
Regulatory compliance support
Real-world data collection
Safety documentation and case processing
Collaboration with Medical Affairs teams
Maintaining quality clinical records

Eligibility Criteria

M.Pharm degree
Pharm.D degree
Freshers are encouraged to apply
Strong communication and documentation skills
Interest in Clinical Research and Drug Safety

REQUIRED VERIFIED SKILLS

Pharmacovigilance
Clinical Research
Drug Safety
Documentation

COMPENSATION & REWARDS

2.5L - 3.5L per annum
The expected salary range for this role is ₹2.5 LPA – ₹3.5 LPA. Actual compensation may vary depending on company policies and candidate evaluation.

ORGANIZATION CONTEXT & CULTURE

Immuneel Therapeutics Pvt. Ltd. is actively hiring for this position.

INDUSTRY: Technology

EXPECTED CAREER ROADMAP

This role provides an excellent foundation for professionals planning a career in Clinical Operations, Pharmacovigilance, Medical Affairs, Clinical Development, Regulatory Affairs, Drug Safety, and the Biotechnology Industry. Benefits include hands-on industry exposure, practical Pharmacovigilance training, Medical Affairs experience, and exposure to innovative therapies.

APPLICATION ADVISORY

Highlight your academic exposure to Oncology, Immunology, or Gene Therapy in your resume. Ensure your resume showcases your understanding of Pharmacovigilance and Clinical Research basics. Prepare for an in-person interview focusing on clinical documentation and AE reporting scenarios.

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.