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If you’re a Life Science or Pharmacy graduate looking to begin a career in clinical research, this Clinical Research Coordinator (CRC) Internship + Diploma Program at SMOConnect Clinical Research Services Pvt. Ltd. is a strong industry-aligned opportunity.
This role offers real-world exposure to ICH-GCP guidelines, ethics committee coordination, investigational product management, and eCRF handling—skills highly valued in the CRO and pharma sectors.
Key Responsibilities
As a CRC Intern, you will:
- Maintain source documents, CRFs, Investigator Site File, and all study documents per ICH-GCP standards
- Complete and manage eCRF entries
- Maintain Investigational Product under prescribed temperature conditions
- Assist in site qualification, initiation, monitoring, and close-out visits
- Organize and support Ethics Committee (EC) meetings
- Prepare and submit EC review forms and study documents
- Coordinate with local and central laboratories
- Support safety reporting within regulatory timelines
- Assist in patient recruitment and screening
- Facilitate the Informed Consent Process
Qualifications
- Education: Life Science or Pharmacy graduates
- Experience: Freshers eligible
- Schedule: Full-time, Morning shift (Mon–Sat)
- Location: Calicut, Kerala
Benefits of Joining SMOConnect
- Hands-on training aligned with ICH-GCP and industry best practices
- Exposure to real clinical trial workflow and documentation
- Opportunity to learn CRC responsibilities under expert supervision
- Added value through Diploma in Clinical Research with the internship
- Skill-building that enhances employability in CROs, hospitals, pharma & biotech companies
How to Apply
Email your CV: hrd@smoconnect.com
Subject Line: CRC Internship and Diploma Program
or
Direct Message (DM) to the recruiter.
- Application Deadline: 06/12/2025
- Expected Start Date: 10/12/2025