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Trial Management Associate

New Jersey All, NJ

Post Date: 11/17/2017 Job ID: JN -112017-20448 Job Type: CTA - Clinical
  • Responsible for assisting within a Trial Operations Group with the global trial initiation, conduct and reporting of trial progress by coordinating and performing assigned operational activities
  • Able to mentor Clinical Project Associates and other Trial Management Associates 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
  • 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
Skills:
  • 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
Education:
  • 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

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