Job Description

Position Description
Main responsibilities include, but are not limited to:

• Product lifecycle management for global clinical trial data collection and management systems

• Reviewing end-user requirements documentation

• Writing test plans and test scripts

• Coordinating end-user testing processes

• Categorizing and resolving system issues

• Managing system changes

• Testing global clinical trial database standards

• Building and maintaining the quality management system for the Global Clinical Data Integration Department

• Supporting internal audits and external inspections of global clinical trial databases and management systems

• Supporting testing and archiving for innovation projects across all global data management departments

• Automating testing processes and applying AI

Qualifications

• Bachelor’s degree or above (majors in Computer Science, Information Technology preferred, also Medicine, Pharmacy, Biology, Public Health, etc.)

• Excellent English speaking and writing skills, CET-6 or above

• Outstanding communication skills, able to coordinate cross-country and cross-department collaboration

• Strong conflict management and problem-solving abilities

• Willingness and ability to learn new knowledge and technologies

• Familiarity with at least one programming language or product application, such as Python, SAS, SQL, PL-SQL, Java, VBA, JIRA, Robot Framework, Power BI/Apps; or knowledge of any of the following regulations or guidelines: drug development process, ICH GCP, GCDMP, or product lifecycle management (SDLC), GAMP, etc.

R368387

Required Skills:

Database Development, Data Processing, Data Review, Data Validation, Data Visualization, Electronic Data Capture (EDC), Global Product Management, Management Process, PL/SQL (Programming Language), Python (Programming Language)

Preferred Skills:

Data Compilation, Data Management, Requirement Documents, Software Development Life Cycle (SDLC)

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:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

12/31/2025

*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.