Data Manager III - Remote Clinical Data Lead

The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc.; Bethesda (MD); Remote; USD 78,000 - 105,000; Full time

Benefits offered by this job

Medical, dental, and vision coverage

Retirement plans

Health savings account

Training and development opportunities

Job summary

The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. seeks a Data Manager III to oversee data management for research projects with CDP in Bethesda, MD.

You will design data collection tools, maintain data management plans, and generate reports while ensuring QA and regulatory alignment. Responsibilities include coordinating across study teams, training site personnel, and managing complex, multi-site studies under FDA/ICH guidelines.

Qualifications

• Bachelor's degree required; Master's preferred.
• Minimum 6–8 years of experience in data management for clinical studies.
• Advanced knowledge of REDCap and clinical data management practices.
• Experience with multisite data management within regulated environments.
• Familiarity with FDA/ICH regulatory requirements and GMP basics.

Responsibilities

• Manage all data-related aspects of clinical trials and data management plans.
• Develop data collection instruments and data entry guidelines.
• Coordinate study team activities and generate data reports.
• Ensure QA, data validation, and data clarification resolution.
• Provide site training and ensure regulatory compliance.

Skills

Clinical Data Management

REDCap

Multisite data management

Statistical software (SAS, Python, R,/

FDA/ICH regulatory knowledge

Good Clinical Practices

Security clearance readiness

Education

Bachelor's degree required

Master's degree preferred

Tools

REDCap

SAS

Python

MATLAB

R

Job description

The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. seeks a Data Manager III to oversee data management for research projects with CDP in Bethesda, MD.

You will design data collection tools, maintain data management plans, and generate reports while ensuring QA and regulatory alignment. Responsibilities include coordinating across study teams, training site personnel, and managing complex, multi-site studies under FDA/ICH guidelines.