Clinical Data Management & Analytics Specialist

MSD Malaysia; Rahway (NJ); Hybrid; USD 72,000 - 113,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Retirement benefits

401(k)

Paid holidays

Vacation

Sick days

Job summary

Merck & Co. in Rahway, NJ seeks a clinical programming professional to deliver reporting and analytics across Oracle, Veeva, and external data for clinical studies.

You will design, build, test and document data reviews per GCDM/CR/GS specifications, ensuring timely data availability and quality. You will support data cleaning, medical review, clinical monitoring and safety reporting, while documenting change requests and participating in improvement initiatives.

Qualifications

• Education in mathematics, science, healthcare or computer science or equivalent pharma skills.
• Strong technical proficiency in clinical data management and reporting systems.
• Exposure to FDA/GxP guidelines and SDLC knowledge; ability to learn new tools quickly.

Responsibilities

• Lead development and maintenance of clinical programming deliverables including reporting and analytics.
• Collaborate with GCDM, CR, and GS to design, build, test and document data reviews.
• Assess feasibility of study team proposed programming and implement technically.
• Support data cleaning, medical review, clinical monitoring and safety reports.
• Document change requests, incident reports and participate in improvement initiatives.

Skills

Adaptability

Analytical Problem Solving

Clinical Data Management

Data Analysis

FDA Regulations

GxP

SDLC

Teamwork

Independent Work

Education

B.A. or B.S. in mathematics, science, healthcare or computer science

Tools

PowerBI

SQL/PL SQL

Databricks

Python

SAS

Job description

Merck & Co. in Rahway, NJ seeks a clinical programming professional to deliver reporting and analytics across Oracle, Veeva, and external data for clinical studies.

You will design, build, test and document data reviews per GCDM/CR/GS specifications, ensuring timely data availability and quality. You will support data cleaning, medical review, clinical monitoring and safety reporting, while documenting change requests and participating in improvement initiatives.