Clinical Data Manager (Multiple Openings)

NSF International • Germantown, MD

12h

About The Position

With a legacy spanning more than 80 years, NSF leverages science and innovation to improve human and planet health. We provide science-driven, independent testing, inspection, certification, and advisory services and develop the very standards that drive the food, water, and life sciences industries worldwide. We empower our clients to navigate shifting regulations to improve consumer health, safety, and quality of life.
One of our core values is We Are One NSF. This means that while we’re one team, we embrace the cultural, ethnic, language, and demographic diversity that reflects the societies in which we live and work.
Come join a team that makes a difference in the world. More information about NSF can be found at nsf.org.
NSF is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, color, religion, sex, sexual orientation, gender identity, national origin, age, status as a protected veteran, or disability.
Notice to Agency and Search Firm Representatives: Please note that NSF is not accepting unsolicited resumes from agencies/search firms for this role. Resumes submitted to an NSF employee by a third-party agency without a valid written & signed search agreement between NSF and said third-party agency will become the sole property of NSF. No fee will be paid if a candidate is hired as a result of an unsolicited agency or search firm referral. Thank you.

From research to patient, NSF's expert team provides comprehensive regulatory, quality and clinical support to pharmaceutical, biotech, medical devices, in-vitro diagnostics, and combination products clients across the product life cycle to navigate complex regulations and industry challenges.

Responsibilities

• Design, develop, and manage Electronic Data Capture (EDC) systems and electronic Case Report Forms (eCRFs) for clinical studies.
• Develop and implement data validation checks to ensure data integrity, accuracy, and completeness.
• Identify, investigate, and resolve data discrepancies in collaboration with clinical, biostatistics, and programming teams.
• Conduct database lock activities, including reconciliation, cleaning, and final data review.
• Ensure compliance with regulatory requirements (FDA, ICH-GCP) and company Standard Operating Procedures (SOPs).
• Collaborate with cross-functional teams, including biostatisticians, clinical operations, and project managers, to support clinical trial data management activities.
• Provide data management input in study protocols, case report forms, and study plans.
• Generate reports, listings, and summaries to track data status and quality.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed