Clinical Trial Associate

  • location: Bridgewater, NJ
  • type: Contract
  • salary: $46.63 - $54.86 per hour
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job description

Clinical Trial Associate

job summary:






 
location: Bridgewater, New Jersey
job type: Contract
salary: $46.63 - 54.86 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
  • Accountable of the customization and regular update of the activities/workpackages under his/her perimeter
  • Ensure the project strategy is reflected in terms of Planning into the operational plan in the customization horizon in consistency with resources and costs aspects
  • Play an OPCM Leader role for the clinical studies, coordinating activities from Clinical Supply and TMED (CSD and PK) OPCM teams (Operational impact management and PPM interface )
  • Analyze the project deliverable timelines and critical path activities
  • Communicates planning information across the Clinical Sciences & Operations platform and to any key IPOM OPCM interfaces or Regulatory OPM as needed
  • Identifies and anticipates any deviations, alerts key IPOM OPCM interfaces or Regulatory OPM in case of major events having an impact on project milestones and propose recommendations / facilitate decision making
  • Provide reporting and analysis to support the project team and operational teams, including during project meetings
  • Ensure a dedicated communication with the Capacity Management team within CSO OPCM group and Clinical Trial Finance (CTF) team in Finance.
  • Ensure history data follow-up in the planning tool and coordinate quality controls of planning data
  • Once agreed with Project actors, CSO OPCM is the single accountable person for the accuracy of the plan entered, its customization in the planning tool.
 
qualifications:
  • General knowledge on overall R&D Drug Development and good knowledge in Business operational activities (clinical trial execution)
  • General knowledge on Project Management methodology
  • Strong knowledge in planning & management and tools
  • Analytical, synthesis and reporting skills
  • Excellent organizational skills, rigor, striving for results, high accuracy orientated
  • Strong communication skills and interpersonal relationship demonstrated
  • General knowledge in resources and capacity management
  • Excellent presentation skills (verbal and written)
  • Fluent in speaking English (verbal and writing)
  • Strong Networking skills
  • Desired Skills: Knowledge of OPX2 Knowledge of databases
 
skills: Clinical Study Design, Clinical Supply Chain
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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