Specialists, Clinical Data Management

MSD; Rahway (NJ); Hybrid; USD 87,000 - 137,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Medical, dental, vision insurance

401(k)

Paid holidays and vacation

Job summary

MSD in Rahway, NJ seeks a Clinical Data Management Specialist to lead data programming, reporting, and analytics for our clinical studies using Oracle and Veeva platforms.

You will design data review processes, validate study programming, support data cleaning, medical review, and safety reporting, while collaborating across study teams to ensure timely, high-quality insights.

Qualifications

• Experience in clinical data programming, data engineering, or clinical operations.
• Strong knowledge of SDLC and system validation.
• Ability to communicate with cross-functional teams and study teams.

Responsibilities

• Design, build, test, and document data review based on specifications.
• Review feasibility of programming/reporting and implement changes.
• Support data cleaning, medical review, monitoring, and safety reporting.
• Provide ongoing support for in-life reports and process improvements.
• Document change and incident reports and escalate as needed.
• Participate in task forces, automation, testing, training, and mentoring.

Skills

Clinical Data Management

Python

SAS

SQL/PL SQL

Power BI

Databricks

AI tools

Communication

Team collaboration

Education

Associate degree in relevant field

Bachelor’s degree in clinical data programming or related field

Advanced degree (Master/PhD) in clinical development or related field

Tools

Databricks

Python

SAS

SQL

Power BI

Job description

Job Description

Join our team as a Specialists in Clinical Data Management to support our clinical studies. In this role, as a Clinical Data Management Specialist, you’ll assumes the responsibilities for all clinical programming (including reporting and analytics) deliverables including Oracle, Veeva platforms along with the external data captured in support of the clinical studies.

Primary activities include, but are not limited to:

Coordinates and participates in the following activities:

• Design, build, maintain, test, and document data review based on written specifications established by Global Clinical Data Management, Clinical Research and Global Safety.
• Review the technical feasibility of study team proposed programming/reporting and technically implement them. Work effectively among teams to communicate issues and ideas to improve business along with understanding of Protocol.
• Support the development & reporting for data cleaning, medical review, clinical monitoring, and safety reports for quality and timely availability in support of our customer needs.
• Perform ongoing support for In-Life Reports.
• Change Requests and Incident Reports are fully documented, signed off, tracked, and reported to upper management.
• Participate in extra activities including, but not limited to, study improvement task forces, automation, initiatives, testing of new systems, and ongoing training and mentoring.

Education:

• Associate degree with a minimum of 3 years’ experience working in clinical data programming, data engineering, or related data-management/clinical operations functions OR
• Bachelor’s Degree with a minimum of 2 years’ experience working in in clinical data programming, data engineering, or related data-management/clinical operations functions OR
• Advanced Degree (master’s or doctorate) with prior experience in clinical development and / or clinical data programming, data engineering, or related data-management/clinical operations activities preferred.

Required Knowledge and Skills:

• Strong technical proficiency in Clinical Data Management/Reporting Systems like Databricks, Python, SAS, SQL/PL SQL, Power BI, etc along with AI related tools.
• Solid knowledge of MS Windows/Office software and exposure to web-based applications.
• Solid knowledge of System Development Lifecycle Management / system validation knowledge.
• Ability to establish and maintain good working relationships with different functional areas.
• Strong sense of urgency and customer focus.
• Excellent communication skills and interacts effectively with Study Team.
• Strong organizational and problem-solving skills.
• Desire and ability to learn new processes and technologies.
• Ability to multi-task, work independently, and good communication skills.
• Understanding of drug discovery process, FDA regulations, GxP guidelines, ICH.

Required Skills:

Clinical Data Management, Communication, Computer Programming, Data Analysis, Data Management, Data Quality Assurance, Electronic Data Capture (EDC), PL/SQL (Programming Language), SQL Databases, Team Communication

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is

$87,300.00 - $137,400.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits

San Francisco Residents Only:

We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:

We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

08/30/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.