Clinical Trial Coordinator Intern

About the role

MSD offers a Clinical Trial Coordinator internship in Hod Hasharon, Israel, providing learning, mentoring and hands-on work experience in clinical trials. The internship lasts up to 12 months in a full-time, office-based position and covers trial and site administration, regulatory and finance, and supply and CRA support. It is an intern/co-op fixed-term position.

Key responsibilities

• Trial and site administration: track and report documents such as safety reports, collate and distribute study tools, update clinical trial databases (CTMS) and trackers, manage clinical and non-clinical supply, and handle labeling requirements and translation change requests.
• Document management: prepare documents and correspondence, collate, distribute, ship and archive clinical documents (e.g. eTMF), assist with eTMF reconciliation and quality control, update manuals such as patient diaries, prepare investigator trial files, obtain document translations and record proper destruction of clinical supplies.
• Regulatory and site start-up: provide and collect forms and lists for site evaluation, validation and submission, track and update study insurance certificates, support IRB/ERC and regulatory agency submissions, and publish study results where required by local law.

Required profile

• B.A./B.S. in Life Sciences (preferred) or equivalent healthcare experience.
• GCP course or CRA course.
• Fluent in local languages and business-proficient in English (verbal and written).
• Effective time management, organization, interpersonal and conflict management skills.