Clinical Research Internship at MSD | Intern Opportunity in Israel
Launch your professional journey in clinical research with a dynamic, hands-on internship designed for ambitious life science graduates. This role provides a comprehensive introduction to clinical trial operations and site management, making it an ideal opportunity for those seeking a Clinical Research Internship in a global, fast-paced environment. Gain real-world experience, collaborate with industry leaders, and take meaningful steps toward a future in clinical development.
About the Company
MSD (Merck Sharp & Dohme) is a global leader in healthcare innovation, committed to advancing clinical research, patient safety, and scientific excellence. With a strong international presence, MSD offers structured training and mentorship through Internships at MSD, empowering early-career professionals to gain critical hands-on experience. The organization fosters collaboration, integrity, and scientific innovation, making it an ideal place for individuals seeking a high-impact Clinical Research Internship or future clinical operations roles.
Internship Details:
- Intern Title: Clinical Trial Coordinator Intern
- Location: Hod Hasharon, Central District, Israel
- Job Type: Full-Time
- Employee Status: Intern/Co-op (Fixed Term)
- Requisition ID: R376610
- Job Posting End Date: 12/23/2025
- Duration: Up to 12 months (Gain experience across trial administration, documentation, regulatory support, and site start-up activities.)
About the Role
Join Global Clinical Trial Operations (GCTO) as a Clinical Trial Coordinator (CTC) Intern. This internship provides hands-on experience, mentorship, and exposure to real-world clinical trial operations. Interns support trial and site administration under the supervision of COM Leads/COMs and CTCs.
What You Will Learn & Do in Clinical Research Internships
Trial & Site Administration
- Track essential documents and safety reports.
- Collect and distribute study documents.
- Update clinical trial databases and trackers.
- Coordinate clinical and non-clinical supply management (when applicable).
Document Management
- Prepare correspondence and trial documents.
- Assist with eTMF reconciliation.
- Update manuals and study materials (e.g., patient diaries, instructions).
- Prepare Investigator Trial File binders.
Regulatory & Site Start-Up Support
- Provide and collect forms for site evaluation, validation, start-up, and submissions.
- Track and update study insurance certificates.
- Support the preparation of IRB/ERC submission packages and regulatory submissions.
Core Competency Expectations
- Fluency in local languages and proficiency in English (written & verbal).
- Strong communication skills.
Behavioral Competencies
- Effective time management and organization.
- Strong interpersonal and conflict-management skills.
Educational Requirements
- B.A./B.S. (Life Sciences preferred) or equivalent healthcare experience.
- Completion of a GCP course or CRA course.
Required Skills for Clinical Research Internships
- Accountability
- Clinical Research & Clinical Trials
- Data Analysis
- Database Management
- Communication
- Cloud Data Catalog
Additional Information
- No relocation or visa sponsorship is provided.
- Flexible work arrangements not applicable.
- Valid driving license and hazardous materials handling not specified.
