Clinical Data Manager

Mmsh Clinical Research; United States; Hybrid; USD 65,000 - 90,000; Full time

Job summary

Mmsh Clinical Research in the United States is seeking a Clinical Data Manager to contribute to eCRF development, data validation, and study-wide reporting to ensure high-quality datasets for analysis.

The role emphasizes hands-on data management, UAT participation, and training site support within a CRO-focused environment, offering opportunities to advance skills in data standards and regulatory compliance.

Qualifications

• Bachelor's degree in a scientific, medical, or clinical discipline is required; Master’s or PhD preferred.
• 2–6 years of previous experience in clinical data management.
• Hands-on experience with clinical trials and pharmaceutical development is preferred.
• Experience in the pharmaceutical or CRO industry is required; strong attention to detail is essential.

Responsibilities

• Contribute to developing eCRFs, CRF Completion Guidelines, edit check specs, and DMP.
• Work on study tracking and metric reports for the study team.
• CRF tracking, data entry, external data integration, data validation and query processing.
• Support UAT of EDC and integrated systems, including test plan execution.
• Assist with training sites/users on EDC applications and UAT.
• Enhance end-user knowledge for study conduct activities, including queries management and reporting.
• Learn to develop data entry screens, dynamics, and edit checks in EDC.

Skills

Data analysis

Problem-solving

Attention to detail

Query & discrepancy management

Clinical data management

Communication skills

Education

Bachelor's degree in a scientific, medical, or clinical discipline

Master's or PhD preferred

Job description

Job Responsibilities

• Contribute to developing eCRFs, CRF Completion Guidelines, Edit check specs, and DMP.
• Contribute to study tracking and metric reports for use by the study team
• Contribute to CRF tracking and data entry, integration of external electronic data, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits.
• Contribute to user acceptance testing (UAT) of EDC and integrated systems including executing of test plan and scripts.
• Assist with preparation for training sites/users training on EDC applications, and UAT.
• End user knowledge for study conduct activities including queries management, standard reporting and extracting data.
• Learning to develop data entry screens, dynamics, edit checks and other EDC components.

Job Requirements

• Bachelor s Degree in a scientific, medical, or clinical discipline or related field is required; Master s or PhD preferred
• 2-6 years of previous experience in clinical data management
• Hands-on experience with clinical trials and pharmaceutical development preferred
• Effective problem-solving and data analysis skills
• Experience in the pharmaceutical or CRO industry must
• Experience with query and discrepancy management required
• Has a strong attention to detail

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