Clinical Data Management Specialist — Data Analytics

Merck; Rahway (NJ); On-site; USD 72,000 - 113,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k)

Paid vacations

Job summary

Merck in Rahway, NJ seeks a clinical programming professional to deliver all reporting and analytics for clinical studies, including Oracle, Veeva platforms, and external data. You will design, build, test, and document data reviews based on written specifications, supporting data cleaning, medical review, clinical monitoring, and safety reporting.

Required are strong SQL/Python/PowerBI skills, knowledge of SDLC and GxP, and familiarity with FDA regulations.

Qualifications

• Bachelor level degree in a related field or pharma skills and experience.
• Strong technical proficiency with clinical data management/reporting systems.
• Experience with SDLC, GxP, FDA regulations, and cross-functional collaboration.

Responsibilities

• Lead design, build, test, and document data reviews for clinical studies.
• Support data cleaning, medical review, clinical monitoring, and safety reporting.
• Provide ongoing support for in-life reports and change/incident requests.
• Participate in automation, testing, and training initiatives.

Skills

Clinical programming

PowerBI

SQL/PLSQL

Python

SAS

Databricks

Education

B.A./B.S. degree

Tools

Oracle

Veeva

Job description

Merck in Rahway, NJ seeks a clinical programming professional to deliver all reporting and analytics for clinical studies, including Oracle, Veeva platforms, and external data. You will design, build, test, and document data reviews based on written specifications, supporting data cleaning, medical review, clinical monitoring, and safety reporting.

Required are strong SQL/Python/PowerBI skills, knowledge of SDLC and GxP, and familiarity with FDA regulations.