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 Clinical Study Conduct Manager

Details
Country: USA
Location: TX San Antonio
Total applied: 5

Relevant Work Experience: 2+ to 5 Years
Career Level: Manager (Manager/Supervisor of Staff)
Education Level: Bachelor's Degree
Job Type: Employee
Job Status: Full Time

Clinical Study Conduct Manager

Join the new team at CEDRA Clinical Research, LLC. CEDRA Clinical Research, LLC, a clinical research organization servicing the pharmaceutical and biotech industries. CEDRA Clinical Research, LLC has opened in San Antonio a new state of the art 200 bed Phase I research facility and has the following position available:

Study Conduct Manager


The Study Conduct Manager will be responsible for hiring and supervising Assistant Coordinators, Coordinators and PRN Coordinating staff. Assures that Coordinators and Assistant Coordinators are trained, prepared and informed about managing a Phase I-IV clinical research trials. In addition he/she will be responsible for working as a team with other departments in the conduction of clinical trials. Oversees all the studies to assure they are conducted and enrolled in the most efficient manner. QC all source documents prior to being used on a study. May run a study during peak times and cover study procedures or shifts as needed. Work schedule will vary and include some weekend work - must be flexible.

Required Education: Bachelor degree in a life science and have at least 4 years of clinical research experience. Preferred Experience: Bachelors degree (preferably in the field of Health); five or more years of clinical research experience; 2 years of supervisor experience.

Award winning benefits package includes 401K performance incentive plan, childcare reimbursement, and tuition reimbursement. Fill out application on line, email or fax to:

CEDRA CLINICAL RESEARCH, LLC
Human Resources Dept.
2455 N. E. Loop 410, Ste 150
San Antonio, TX 78217
Fax 210 635-1646
csikora@cedracorp.com
www.cedraresearch.com

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