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The Clinical Data Manager is responsible for the collection, management, and quality control of clinical trial data. This role ensures data accuracy, consistency, and compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP).
Responsibilities:
Design, develop, and maintain clinical databases and CRFs
Oversee data entry, validation, and query resolution
Ensure data quality and integrity throughout the study lifecycle
Collaborate with clinical, biostatistics, and regulatory teams
Prepare and deliver clean datasets for analysis and reporting
Skills & Experience:
Bachelor’s degree in life sciences, computer science, or related field
Experience in clinical data management and EDC systems
Knowledge of GCP, CDISC standards, and regulatory requirements
Strong attention to detail and organizational skills
EEO Employer
We are an equal opportunity employer and comply with all applicable federal, state, and local fair employment practices laws. We strictly prohibit and do not tolerate discrimination against employees, applicants, or any other covered persons because of race, color, religion, creed, national origin or ancestry, ethnicity, sex, sexual orientation, gender (including gender identity and expression), marital or familial status, age, physical or mental disability, perceived disability, citizenship status, service in the uniformed services, genetic information, or any other characteristic protected under applicable federal, state, or local law. Applications from members of minority groups and women are encouraged.
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