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Clinical Trial Administrator III Bridgewater United States,  

Aequor Technologies (company)


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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