Manager, Research Study Activation

Posted 1hrs ago

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Job Description

Manager of Study Activation overseeing overall study activation activities at Sarah Cannon Research Institute. Driving new initiatives and relationship management with sites and partners in oncology research.

Responsibilities:

  • Responsible for overall study activation activities, including direct supervision and development of staff
  • Provide leadership in the study start-up, to include trials in lead, opportunity and selection.
  • Liaise with site, sponsor and CRO contacts to establish and maintain key organizational connectivity through study start-up
  • Support the overall site evaluation process from review of opportunity to executive leadership recommendation
  • Interface with Sarah Cannon lines of business to develop/foster relationships and understanding of business line needs.
  • Facilitate business development and relationship management activities with pending and active sites and pharma/CRO partners.
  • Utilize metrics to drive improvement strategies trial activations for sites and site, sponsor and CRO partner relationships.
  • Escalate unresolved issues to Senior Manager or appropriate level of management.
  • Drive new initiatives and special projects as directed by Senior Manager, Site Relationships and Support Services.
  • Assess organizational processes associated with startup and support to identify ways to improve and streamline processes.

Requirements:

  • Clinical and/or scientific experience in a research setting required
  • Research certification (ACRP or CCRP) preferred
  • The ability to read, understand, and comply with research protocols.
  • Knowledge of FDA guidelines and GCP.
  • Resourceful with heightened analytical abilities and problem solving skills in a fast paced environment.
  • Excellent interpersonal skills, detailed-oriented and meticulous.

Benefits:

  • Comprehensive benefits to support physical, mental, and financial well-being.