INTERNSHIP DETAILS

Clinical Research Intern

CompanyMSD
LocationDimos Alimos
Work ModeOn Site
PostedMarch 16, 2026
Internship Information
Core Responsibilities
This role involves supporting and collaborating with local GCTO stakeholders to ensure the smooth execution of clinical studies, including assisting CRAs/CTCs with daily activities. Responsibilities also cover supporting the collection, review, and monitoring of essential study documentation across start-up, maintenance, and close-out phases.
Internship Type
full time
Company Size
40979
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
About the Role

Job Description

We are seeking two (2) motivated Clinical Research Interns to join our team. These internships aim to equip the candidates with essential skills for the successful execution of clinical study activities.

Responsibilities:

This role will support and collaborate with GCTO stakeholders at local level to ensure the smooth conduct of clinical studies.

  • Assist CRAs/ CTCs with daily study activities.
  • Support the collection, review, and monitoring of essential documentation for the study start-up, maintenance, and close-out phases.
  • Support with the preparation of regulatory documentation for studies in the validation phase.
  • Assist with document management within electronic Trial Master Files (eTMF) and electronic Investigator Site Files (eISF), including the preparation, distribution, and archiving of clinical documents.
  • Assist to management and maintenance of information in CTMS, CLMS and various other systems as appropriate and per timelines.
  • Support System SMEs in system clean-up activities.
  • Support the collection of information necessary for budget customization.
  • Provide assistance for various study tasks, as needed, in collaboration with other sponsor roles to achieve study milestones effectively.

Profile:

  • Certificate in scientific disciplines or Bachelor’s degree in Life Sciences, Nursing, or a related field preferred
  • Active participation in a MSc program in Clinical Research or related fields.
  • Proficiency in Microsoft Office applications (Word, Excel, Email).
  • Good knowledge of the English language.
  • Strong analytical skills with attention to detail, organizational abilities, proactivity, and problem-solving skills.
  • Strong organizational skills and ability to work both independently and collaboratively within a team environment.
  • Excellent communication skills and a team-oriented mindset with flexibility and dynamism.

Required Skills:

Accountability, Clinical Research, Cloud Data Catalog, Data Analysis, Database Management, Data Science, Data Security, Data Visualization, Data Wrangling, Detail-Oriented, Event Planning, Investigation Procedures, IS Audit, Key Performance Indicators (KPI), Project Management, Python (Programming Language), Software Proficiency, Vendor Relationship 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:

03/30/2026

*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.

Key Skills
AccountabilityClinical ResearchCloud Data CatalogData AnalysisDatabase ManagementData ScienceData SecurityData VisualizationData WranglingDetail-OrientedEvent PlanningInvestigation ProceduresIs AuditKey Performance IndicatorsProject ManagementPython
Categories
Science & ResearchHealthcareAdministrative