INTERNSHIP DETAILS

Assoc. Spclst, Medical Affairs ONC Intern

CompanyMSD
LocationHong Kong
Work ModeOn Site
PostedSeptember 2, 2026
Internship Information
Core Responsibilities
The intern will support medical affairs projects through literature reviews and data analysis while assisting the regulatory team with product registration and documentation. Responsibilities also include administrative tasks, project tracking, and participating in field visits to understand clinical treatment landscapes.
Internship Type
full time
Company Size
39672
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

Overview:

 

The internship will be jointly offered by medical affairs and animal health regulatory affairs teams.

 

As a Medial Affairs Intern, you will have exposure and understanding on clinical landscape in key therapeutic area. The

internship provides practical experience in medical affairs work and scientific engagement with local physicians under

supervision. The intern is expected to spend around one-third of the time with medical affairs team.

 

As a Regulatory Affairs Intern, you will support the regulatory team in various administrative tasks related to product

registration and compliance in Animal Health. This internship offers practical experience in regulatory documentation and

understanding local regulatory requirements under supervision. The intern is expected to spend around two-third of the

time with regulatory affairs team.

 

Main Responsibilities: Main responsibilities include but are not limited to:

 

Key responsibilities:

 

Medical Affairs

· Support medical affairs projects, including literature reviews, data analysis, and preparation of scientific

materials (e.g., slide decks, educational resources)

· Perform administrative duties such as project tracking, documentation, and meeting scheduling

· Join field visit with medical team and understand the latest clinical treatment landscape

 

Regulatory Affairs

· Assist in compiling and organizing regulatory documents and registration dossiers.

· Support preparation of local package inserts and packaging components under guidance.

· Help maintain and archive regulatory documentation and databases accurately.

· Collect and summarize regulatory data for reporting

 

Competencies/ Skills:

Expectations:

· Proficient in reading and writing in English to accurately understand and prepare regulatory documents.

· Self-motivated candidate to learn and work collaboratively.

· Detail-oriented with good organizational skills.

· Ability to communicate clearly and professionally with team members.

Required Skills:

Advisory Board Development, Advisory Board Development, Audit Trails, Clinical Marketing, Communication, Data Generation, Data Reporting, Detail-Oriented, Emergency Medicine, File Management, Government Regulation, Healthcare Education, Healthcare Market, Investigator-Initiated Studies (IIS), Legal Compliance, Life Cycle Support, Medical Knowledge, Medical Literature Review, Medical Marketing Strategy, Medical Procedures, Pharmacy Benefits Management (PBM), Project Tracking, Proper Documentation, Regulatory Affairs Management, Regulatory Management {+ 9 more}

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:

09/4/2026

*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
Regulatory AffairsMedical AffairsData AnalysisProject TrackingDocumentationLiterature ReviewCommunicationDetail-OrientedRegulatory ComplianceClinical LandscapeScientific EngagementData ReportingFile ManagementHealthcare MarketMedical Knowledge
Categories
HealthcareScience & ResearchAdministrativeLegal