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Clinical Trial Administrator III Bridgewater United States,  


Posted on : 22 December 2017

Project Description

The TMAIII is responsible for assisting the CTM/CDM/CTOM/TL/GL within a Trial Operations Group dedicated to a Therapeutic Area BU or across one or more TSUs/DPUs/GMA/USMA, etc. in a specific geographical site with the global trial initiation, conduct and reporting of trial progress by coordinating and performing assigned operational activities. The TMAII may need to take-on CPA level administrative tasks as required to meet business needs and to support a customer-oriented approach for Trial Operations. Able to mentor CPAs and other TMAs as appropriate. Able to proactively identify and propose solutions to operational activities. Requires minimal supervision for routine responsibilities. Operational Responsibilities to be Conducted in Accordance with established Processes, Policies and Standards which may be delegated/assigned to a TMA II by the Responsible CTOM for (see full job description attached for detail): Study Coordination, Tracking, and Reporting Study Document development Assist with Data Review Communication Filing Study Specific e-room Training Supporting Operational Excellence Meeting business needs and to support a customer-oriented approach for Trial Operations Knowledge and operational experience working in the clinical trial environment Familiarity with Windows-based computer applications (eg, MS EXCEL, ACCESS and Powerpoint) and working in clinical trial management systems (eg, IMPACT) Excellent interpersonal and communication skills (verbal and written) including good English and ability to maintain a high-level of confidentiality Self motivated, detail-oriented, ability to handle multiple tasks efficiently and effectively, and excellent organizational skills required Ability to work effectively in a team Able to mentor CPAs and other TM associates as appropriate. Able to proactively identify and propose solutions to operational activities. USA: Bachelor's degree with 3 years clinical research experience, familiarity with medical terminology, general understanding of the R&D process and previous exposure to GCPs/ICH is required. Pharma experience with global trials/teams required

Locations

NJ - Bridgewater

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