Clinical Research Associate

Skill-First Training: We bridge the gap between your degree and the job market by providing intensive training on industry-standard operations.

Mentorship: Work directly with industry experts who are committed to your professional development.

Hands-on Exposure: Gain practical experience in global clinical trial standards, moving beyond textbook theory.

Clear Growth Path: A structured roadmap within a globally recognized organization designed to evolve you into a seasoned professional.

Key Responsibilities

• Industry Skill Mastery: Actively participate in specialized training sessions to master clinical operations, documentation, and regulatory compliance.
• Site & Documentation Support: Learn to manage Trial Master Files (TMF), site files, and Case Report Forms (CRF) with accuracy.
• Protocol Compliance: Gain a deep understanding of ICH-GCP, ethical guidelines, and local regulatory requirements.
• Operational Assistance: Assist in the daily management of clinical trial activities and patient coordination under the guidance of senior mentors.

Eligibility Criteria (Strictly Freshers)

• Education: B.Pharma, M.Pharma, D.Pharma, and all Life Sciences graduates (B.Sc/M.Sc in Biotechnology, Microbiology, Nursing, Biochemistry, or equivalent healthcare fields).
• Batch: 2024, 2025, and 2026 graduates (Final year students are highly encouraged to apply).
• Experience: Strictly 0 years. We are looking for fresh talent ready to be molded. Candidates with prior professional clinical research experience will not be considered.
• Skills: Exceptional communication, a high level of organization, and a genuine passion for building a long-term career in the life sciences industry.

How to Apply

If you are ready to transition from a student to a professional, we want to hear from you! Join our Fresher Intake Program and let us help you launch your clinical research career.

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