Job Description

CTC Intern

Global Clinical Trial Operations (GCTO)

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 clinical trials.

This program provides comprehensive trial and site administration experience. Under the oversight of the COM Lead/COMs and CTC’s, the person prepares, collates and distributes clinical documents.

Internship Overview

· Internship duration – up to 12 months

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 collection and distributions of study documents

o Update clinical trial databases and trackers

o Clinical supply & non-clinical supply management, in collaboration with other country roles (if applicable)

· Document management:

o Prepare documents and correspondence

o Collect and distribute clinical documents

o Assist with eTMF reconciliation

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

o Prepare Investigator trial file binders

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

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

o Obtain, track and update study insurance certificates

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

CORE Competency Expectations:

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

Behavioural 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

Required Skills:

Accountability, Clinical Research, Clinical Trials, Cloud Data Catalog, Communication, Data Analysis, Database Management

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Intern/Co-op (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

12/23/2025

*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.