Clinical Data Management Specialist: End-to-End Trials

Merck & Co.; West Point (PA); Híbrido; USD 72.000 - 113.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

401(k) retirement benefits

Paid holidays, vacation and sick days

Hybrid work arrangement

Descripción de la vacante

Merck & Co., Inc. is seeking a Clinical Data Manager (CDM) in the West Point, PA area.

You will oversee end-to-end data management activities for clinical trials, including tool development, data integrity review, query management, coding, and database lock preparation, while adhering to SOPs and ICH-GCP guidelines. Key responsibilities include implementing data management tools, running integrity reports, and coordinating with sites and vendors.

Formación

• End-to-end data management for clinical trials.
• Knowledge of SOPs and ICH-GCP guidelines.
• Ability to work under pressure in a changing environment.

Responsabilidades

• Develop and implement data management tools and change requests under guidance.
• Run data integrity check reports per data review plans.
• Raise questions to sites/vendors and verify data corrections.
• Execute user acceptance testing of data management tools.
• Monitor data quality and cycle-time, escalating issues as needed.
• Support study database lock preparation and archiving activities.

Conocimientos

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

Educación

High School Diploma

B.A. or B.S. in Medicine/Pharmacy/Nursing/Biological Sciences/Health care

Descripción del empleo

Merck & Co., Inc. is seeking a Clinical Data Manager (CDM) in the West Point, PA area.

You will oversee end-to-end data management activities for clinical trials, including tool development, data integrity review, query management, coding, and database lock preparation, while adhering to SOPs and ICH-GCP guidelines. Key responsibilities include implementing data management tools, running integrity reports, and coordinating with sites and vendors.