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Roles
Tech stack
Required
Location
Kerala, Kerala, India, Remote (India)
Work setup
- Employment
- full-time
- Level
- Junior
- Remote policy
- Remote (India).
- Remote scope
- country-limited
Role details
Responsibilities
- Actively participate in specialized training sessions to master clinical operations, documentation, and regulatory compliance.
- Learn to manage Trial Master Files (TMF), site files, and Case Report Forms (CRF) with accuracy.
- Gain a deep understanding of ICH-GCP, ethical guidelines, and local regulatory requirements.
- Assist in the daily management of clinical trial activities and patient coordination under the guidance of senior mentors.
Requirements
- 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; prior professional clinical research experience will not be considered.
- Exceptional communication.
- High level of organization.
- Genuine passion for building a long-term career in the life sciences industry.
Application
Please mention the word **POIGNANT** and tag RMTM4LjIwMS4xMjYuMTgx when applying to show you read the job post completely (#RMTM4LjIwMS4xMjYuMTgx). This is a beta feature to avoid spam applicants.
- Portfolio
- unclear
- GitHub
- not required
- Cover letter
- unclear
- Apply flow
- external
Company context
- Industry
- Clinical research (life sciences)
Description
Clinical Research Associate (Trainee/Freshers Only) Organization: Clinogenesis Research Organization Location: Remote (India) Department: Clinical Operations Employment Type: Full-Time About the Role Are you a recent graduate eager to start a career in Clinical Research but finding it difficult to gain entry? Clinogenesis Research Organization is bridging the gap between graduation and professional success. We are offering an exclusive, entry-level Career Launchpad designed specifically for freshers. This is not just a job; it is a dedicated training program where we teach you the actual industry-required skills necessary to excel as a Clinical Research Associate (CRA). Why Join Our Program? - Skill-First Training: intensive training on industry-standard operations. - Mentorship: work directly with industry experts. - Hands-on Exposure: practical experience in global clinical trial standards. - Clear Growth Path: structured roadmap within a globally recognized organization. Key Responsibilities - Actively participate in specialized training sessions to master clinical operations, documentation, and regulatory compliance. - Learn to manage Trial Master Files (TMF), site files, and Case Report Forms (CRF) with accuracy. - Gain a deep understanding of ICH-GCP, ethical guidelines, and local regulatory requirements. - 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; 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 Join our Fresher Intake Program. Please mention the word POIGNANT and tag RMTM4LjIwMS4xMjYuMTgx when applying to show you read the job post completely (#RMTM4LjIwMS4xMjYuMTgx).
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