Clinical Trial Coordinator - Intern

תיאור התפקיד

CTC Intern

The internship program provides learning experience, mentoring and valuable work experience in the field of clinical trials. We provide our interns the opportunity to work on meaningful assignments and make sure that they gain real world experiences (in the areas of Regulatory & Finance and Supply & CRA support).

This program provides comprehensive trial and site administration experience. Under the oversight of the COM Lead/COMs and CTC’s, the person prepares, collates, distributes and archives clinical documents. The Interns supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.

Internship Overview

• Internship duration – up to 12 months, full-time position.

During this program you will learn and experience the following, but are not limited to:

Trial and site administration:

o   Track (e.g. essential documents) and report (e.g. Safety Reports)

o   Ensure collation and distribution of study tools and documents

o   Update clinical trial databases (CTMS) and trackers

o   Clinical supply & non-clinical supply management, in collaboration with other country roles

o   Manage Labeling requirements and coordinate/sign translation change request

Document management:

o   Prepare documents and correspondence

o   Collate, distribute/ship, and archive clinical documents, e.g. eTMF

o   Assist with eTMF reconciliation

o   Execute eTMF Quality Control Plan

o   Update manuals/documents (e.g., patient diaries, instructions)

o   Document proper destruction of clinical supplies.

o   Prepare Investigator trial file binders

o   Obtain translations of documents

Regulatory & Site Start-Up responsibilities: Collaborate with other country roles to:

o   In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions

o   Obtain, track and update study insurance certificates

o   Support preparation of submission package for IRB/ERC and support regulatory agencies submissions.

o   Publish study results for GCTO and RA where required per local legislation

Office-based - Hod Hasharon.

CORE Competency Expectations:

·Fluent in Local Languages and business proficient in English (verbal and written) and excellent communication skills.

Behavioral Competency Expectations:

·Effective time management, organizational and interpersonal skills, conflict management

Educational Requirements:

· B.A./B.S. (Life Science preferred) or equivalent healthcare experience.

· GCP course/ CRA course

Additional location(s) Compensation Information:

Required Skills:

Ability to Coordinate, Ability to Coordinate, Audit Trails, Clinical Databases, Clinical Research, Clinical Supplies Management, Cloud Data Catalog, Conflict Management, Data Analysis, Database Management, Data Destruction, Data Science, Data Security, Data Visualization, Data Wrangling, Detail-Oriented, Documentation Maintenance, Document Management, Document Management Software, Evaluating Applications, Event Planning, Financial Tracking, Healthcare Databases, Insurance Coverage, Insurance Policies {+ 9 more}

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

נציג חברת השמה, אנא קרא בעיון, חברת
Merck & Co., Inc., Rahway, NJ, USA, המוכרת גם בשם Merck Sharp & Dohme Corp., Rahway, NJ, USA, אינה מקבלת סיוע לא מבוקש מחברות השמה להזדמנויות תעסוקה. כל קורות החיים שיוגשו על ידי חברות השמה לעובדים בחברה שלנו, ללא הסכם השמה תקף בכתב, עבור משרה זו, ייחשבו כרכושה הבלעדי של החברה שלנו.  לא ישולמו כל עמלות במקרה של העסקת מועמד לעבודה בחברה שלנו, כתוצאה מהפניה של סוכנות, כאשר לא קיים הסכם תקף מראש. כאשר קיימים הסכמי סוכנות, ההצגה היא ספציפית למשרה. אנא, אין ליצור קשר טלפוני או בדוא"ל.

סטטוס עובד:

מתמחה (Fixed Term)

רילוקיישן:

מתן חסות ל-VISA:

דרישות לנסיעות:

הסדרי עבודה גמישים:

Not Applicable

משמרת:

רישיון נהיגה בתוקף:

חומר(ים) מסוכן(ים):

Job Posting End Date:

11/8/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.