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Clinical Study Manager

Post Date:Jan 03, 2018Type:Full-Time
Start Date:12/29/2017Salary:
Location:US-IL-Libertyville Job Reference:

Qualifications needed for Clinical Study Manager:

  • Bachelor’s Degree, preferably in the life sciences or healthcare field
  • Minimum 4 years as Study Coordinator or related experience required
  • Homecare experience preferred
  • Knowledge of clinical trial terminology and practices highly desirable
  • Some leadership experience
  • Training external and internal team members
  • Excellent judgment and decision-making ability
  • Outstanding communication skills (written and verbal)
  • Well-organized and able to multi-task
  • Able to work independently and as an effective member of a team
  • Superior problem identification and resolution capability
  • Committed and able to produce quality and timely results
  • Takes initiative, proactive , customer service oriented
  • Detail and process-oriented
  • Capable of earning the professional respect of all stakeholders related to a study
  • Demonstrates the ability to build strong positive relationships with others internally and externally
  • Understands and demonstrates compliance with relevant regulations including ICH/GCP, HIPAA, IATA
  • Demonstrates project management skills
  • Proficient with word processing applications

Our client offers great career path, excellent benefits, and a great team culture that is rewarding.    Email resume today to [Click Here to Email Your Resumé]

Job Description:



Clinical Study Manager is needed for a growing company in the pharmaceutical research industry. This is a DIRECT HIRE Opening in central Lake County. The Clinical Study Manager’s primary responsibility is to coordinate and manage all -contracted services in assigned study(s), providing quality service, and exceeding the expectations of our customers.  The Clinical Study Manager manages the key relationships and communication among all internal and external stakeholders involved in a study, keeping all stakeholders informed in a timely and professional manner about the progress and key events with the study.  The Clinical Study Manager is expected to accurately identify issues and creatively resolve problems while correcting processes as needed. 


Clinical Study Manager’s Duties and Responsibilities:

  • Coordinate, administer and document all study management activities to include:
    • Maintain and adhere to study project plans and timelines
    • Train subcontracted resources, country study managers, nurses or other clinicians
    • Provide support and guidance for subcontracted resources, including routine teleconferences to review progress to timelines, issue management, and information sharing
  • Act as the liaison between the sponsor, investigative site staff, laboratory, pharmacy and other internal and external personnel as the study requires
  • Represent company effectively and professionally in project calls, webinars, teleconferences and meetings
  • Recognize sensitive issues and manage them effectively; escalate up when need assistance
  • Comply with ICH/GCP, IATA, HIPAA and other appropriate regulations, policies and procedures
  • Ensure that contracted study visits are completed on schedule, documentation is timely, complete and accurate and lab samples are evaluable
  • Perform other duties as assigned


Contact Information
Express Employment Professionals
Name: Ilene Barry
Ph: 847-816-8422

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