
Clinical Research Professional
2 days ago
Are you eager to launch a career in clinical research?
We offer a fantastic opportunity for fresh graduates to grow in a structured, accredited environment.
Job Description
- Assist with on-site coordination of clinical trial activities under supervision
- Maintain essential documents, site files, and case report forms
- Support the investigator in protocol compliance and patient coordination
- Ensure all trial activities adhere to ICH-GCP and ethical guidelines
- Participate in training sessions and team meetings as part of learning
Key Responsibilities
- On-Site Coordination: Assist with on-site coordination of clinical trial activities under supervision.
- Document Management: Maintain essential documents, site files, and case report forms.
- Protocol Compliance: Support the investigator in protocol compliance and patient coordination.
- Ethics and Guidelines: Ensure all trial activities adhere to ICH-GCP and ethical guidelines.
- Learning and Development: Participate in training sessions and team meetings as part of learning.
Eligibility Criteria
- B pharma, M pharma, B.Sc / M.Sc in Life Sciences, Pharmacy, Nursing, or equivalent healthcare field
- Freshers only
- Strong communication and organizational skills
- Eagerness to learn and grow in the clinical research domain
Why Work with Us?
- Work alongside expert mentors and gain practical exposure
- Structured learning in a globally accredited research setup
- Continuous development and support for long-term career growth
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