Clinical Research Associate Intern

Job Description

Intenship period: 3 Mar 2026 ~ 2 Mar 2027

Job Summary

• Participate in the GCTO Korea Internship Program and support GCTO Korea deliverables under supervision of relevant functional roles.

• Engage in CRA/CTC job shadowing including essential document review and development, participation in mock Site Initiation Visits (SIV), and on-site monitoring training led by preceptors.

Key Responsibilities

• Supply Management

• • Track import, inventory, and distribution of clinical trial supplies

  • Manage ancillary supplies and support related requests

• Essential Documents

• • Prepare and support IRB submissions

  • Perform eTMF uploads and quality control (QC)

  • Support development of subject informed consent forms (ICF)

  • Assist with Investigator Site File (ISF) setup and maintenance

• Safety Reporting

• • Support safety/adverse event reporting processes and documentation

• Clinical System Support

• • Assist with SIP (Shared Investigator Platform) registration and access setup

• Department Connectivity and Events

• • Serve as Viva Engage ambassador (community facilitation and content management)

  • Support department meetings and internal events planning and execution

Qualification

• Bachelor’s degree or higher in Pharmacy, Veterinary Medicine, Nursing, Biotechnology/Life Sciences, or a related field

• Alternatively, expected graduation in February 2026 in the above or related disciplines

Required Skills:

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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Relocation:

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