Sr. Clinical Trial Associate

  • Location
    Madison, New Jersey
  • Job type
  • Category
    Medical & Science - Pharmaceutical - Clinical

A Sr. Clinical Trial Associate job near Morristown, New Jersey is available courtesy of Adecco Medical and Science. This is expected to a long-term contract opportunity with a recognized pharmaceutical company. Minimum of 3 to 5 years of pharmaceuticals/biotech experience. Minimum of 3 to 5 years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials.

Sr. Clinical Trial Associate job responsibilities include:
• Manage study activities for feasibility, allocation of patients, and development of study timelines; this may include study concept/planning/strategy phase, study initiation phase, conduct phase, and close out phase.
• Ensure regional study feasibility in collaboration with study managers including summarizing regional assessment of patients and resources.
• Process and system thinking, customer orientation, and ability to work in multidisciplinary study teams and to execute within a matrix management model, ideally in pharmaceuticals/biotech.
• Experience in execution of clinical research trials, including GCP and regulatory guideline knowledge and audit inspections.
• Knowledge and experience in clinical study budgeting including timeline and the application of clinical trial performance metrics.
• Demonstrated ability to support the development and management of various aspects of the end to end study operational plan.
• Demonstrated ability to support the operational execution and delivery of various aspects of a quality clinical trial.
• Demonstrated experience in change management initiatives preferred.
• Program and project management experience preferred.
• International experience a plus.
• Support development of regional specific study timelines, play a key role in providing accurate trial costs and timeline forecasts.
• Maintains current scientific knowledge relevant to assigned therapeutic areas.

• BS/BA/MS with 2-5 years pharmaceutical industry or clinical medicine experience
• Experience handling/managing a global clinical trials helpful but not required
• Knowledge of drug development and FDA GCP/ICH regulatory guidelines.
• Proficiency with and ability to utilize software applications that support Clinical Operations: Microsoft Word, Excel, PowerPoint; Adobe Acrobat, EDC systems, etc.
• Clinical trial management system (CTMS) background is a plus.

• Direct study management experience with multiple phases preferred

If you are interested in this Sr. Clinical Trial Associate job near Morristown, New Jersey then please click APPLY NOW. For other opportunities available at Medical and Science go to

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Reference number US_EN_2_106405_329967