Clinical Data Manager – End-to-End Trial Data

Merck & Co.; Rahway (NJ); Hybrid; USD 72,000 - 113,000; Full time

Benefits offered by this job

Hybrid

Job summary

Merck & Co. is seeking a Clinical Data Manager to execute end-to-end data management activities across clinical trials. You will develop and validate data management tools, ensure data integrity, and manage queries while adhering to SOPs and ICH-GCP guidelines.

The role requires strong planning, communication, and teamwork in a fast-paced environment. The position involves collaboration with SCDM/LCDM and external vendors, overseeing data quality, and ensuring timely database lock preparations.

Qualifications

• End-to-end data management activities in clinical trials.
• Knowledge of ICH-GCP guidelines and SOPs.
• Strong data integrity review and reconciliation skills.

Responsibilities

• Develop and modify data management tools and systems under guidance.
• Run data integrity check reports per data review plans.
• Query investigational sites and review responses for corrections.
• Test data management tools via user acceptance testing.
• Escalate overdue items and unresolved questions.
• Support CDM with issue resolution before database lock.
• Archive trial documents per SCDM/LCDM directions.
• Monitor data quality and cycle-time performance.
• Communicate project status and risk to senior CDM.

Skills

Adaptability

Analytical Problem Solving

Clinical Data Cleaning

Clinical Data Management

Data Collection Methods

Data Documentation

Data Integrity

Data Processing

Data Reporting

Data Review

Data Validation

Document Management

Good Clinical Practice (GCP)

Project Management

Teamwork

Education

High School Diploma

BA/BS in Medicine, Pharmacy, Nursing, Biological Sciences, or health care related discipline

Job description

Merck & Co. is seeking a Clinical Data Manager to execute end-to-end data management activities across clinical trials. You will develop and validate data management tools, ensure data integrity, and manage queries while adhering to SOPs and ICH-GCP guidelines.

The role requires strong planning, communication, and teamwork in a fast-paced environment. The position involves collaboration with SCDM/LCDM and external vendors, overseeing data quality, and ensuring timely database lock preparations.