Data Manager/Protocol Monitor

Frederick, MD
Sep 05, 2017
Sep 06, 2017
Full Time
The EMMES Corporation, organized in 1977, is a privately owned Contract Research Organization (CRO). Emmes is dedicated to providing statistical and epidemiological expertise, computer systems development, data management, study monitoring, regulatory guidance, and overall operational support to clients engaged in clinical and biomedical research. Emmes is seeking a dependable, detail oriented Data Manager/Protocol Monitor to support all phases of clinical trials.

The Data Management functions include: design, develop and manage Emmes proprietary Electronic Data Capture (EDC) system's electronic Case Report Forms (CRFs) and partner with Project Leaders and other research staff to implement Case Report Forms that adhere to company standard operating procedures and federal guidelines, maintain data integrity, and meet the needs of the clinical study protocol.

The Protocol Monitoring functions include: overall responsibility for planning, monitoring, and coordinating clinical research studies at external trial sites and working closely with internal project members, site study coordinators and investigators to ensure compliance with protocol and overall clinical objectives.

Requirements Strong data management/computer skills; experience with CRF design, EDC systems, or other web based data collection systems helpful Attention to detail, requirements documentation and change management are a necessity Bachelor's degree and related experience in health related field Excellent oral and written communication skills with the ability to effectively communicate and coordinate with internal and external clients and colleagues Willingness to travel as necessary, consistent with the project needs

Emmes has an outstanding benefits package including: generous tuition reimbursement, professional development and training programs.


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Emmes is proud to be an Equal Opportunity Employer. EOE/M/F/D/V

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