Sarah Cannon Research Institute (SCRI) is a global strategic research organization focusing on advancing therapies and accelerating drug development. It is one of the largest clinical research programs, conducting community-based clinical trials in oncology and cardiology through affiliations with a network of more than 700 physicians in the United States and United Kingdom. Additionally, SCRI offers management, regulatory and other research support services to drug development sponsors and strategic investigator sites.
GENERAL SUMMARY OF DUTIES- Will facilitate collaboration between SCRI and clinical trial sponsors to advance common interests and achieve mutual goals including study start up metrics. Will serve as the primary liaison between SCRI Strategic Sites, SCRI Departments, and clinical trial sponsors for identification and resolution of operational issues. Additional duties may be defined per specific Master Service Agreements between SCRI and Pharmaceutical Company sponsors.
DUTIES INCLUDE BUT ARE NOT LIMITED TO:
• Ensures that SCRI Departments and Strategic Sites adhere to sponsor and trial defined performance metrics.
• Develops project status reports and communicates with SCRI Strategic Sites, SCRI Departments, and clinical trial sponsors.
• Tracks performance metrics for SCRI Departments and Strategic Sites.
• Participates in clinical trial sponsor teleconferences and meetings to represent operational issues, study metrics, and enrollment for all SCRI Strategic Sites.
• Attends and participates in all required meetings including Protocol Review and Program Meetings
• Communicates project resource requirements to SCRI Strategic Sites and assists in establishing contingency plans for key resources.
• Works with SCRI Strategic Sites to identify project related issues and facilitate resolution.
• Provides proactive and creative recommendations on how to meet study specific goals.
• Builds and maintains strong relationships with clinical trial sponsors for the success of clinical trial management.
• Communicate and escalate unresolved issues at the appropriate time and to the appropriate level of management.
REQUIREMENTS FOR CONSIDERATION
• Demonstrated ability to coordinate operational issues and support across multiple sites for multiple oncology clinical trials.
• Demonstrated leadership and problem solving abilities
• Demonstrated ability to manage and prioritize assigned projects
KNOWLEDGE, SKILLS & ABILITIES
• Proven knowledge of FDA guidelines and GCP is required.
• Excellent professional writing and communication skills.
• Excellent organizational and prioritizing capabilities.
• Resourceful with heightened analytical abilities and problem solving skills in a fast paced environment.
• Strong computer skills with demonstrated ability using clinical trial databases, electronic data capture, MS Access or Excel.
• Excellent interpersonal skills, detailed-oriented and meticulous.
• High school diploma required.
• Bachelor’s degree in nursing, pharmacy or other science related field or combination of equivalent education and experience required.
• 3 years experience in healthcare research or other science related field.
• 3 years experience in a clinical trial environment
• LPN or RN preferred
• Research Professional Certification- CCRP or exam eligibility preferred
HCA Inc - 7 months ago