Sr. Clinical Research Lead

The CRC III Lead will perform lead duties guiding a team of clinical research coordinators. This position will be responsible for managing clinical trial projects and ensuring enrollment numbers are achieved and compliance is adhered to. This person will assist with the day to day activities of individual clinical trials and will ensure compliance at all levels.

Outstanding UA benefits include health, dental, and vision insurance plans; life insurance and disability programs; paid vacation, sick leave, and holidays; UA/ASU/NAU tuition reduction for the employee and qualified family members; retirement plans; access to UA recreation and cultural activities; and more!

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Study coordination and day-to-day oversight:

• Identify and monitor barriers to enrollment and retention
  and develop solutions to enroll. Ensure local strategies are successful through
  regular assessment and evaluation.
• Daily oversight of study coordination.
• Regularly meet with PIs to discuss enrollment and provide
  and receive updates on study status.
• Ensure staff adhere to study guidelines

Team:

• Communicate with assigned teams regularly via huddles or
  meetings in order to share updates, process changes, etc.
• Ensure staffing is appropriate to meet business needs,
  review and coordinate sick & vacation requests.
• Plan and lead the work of multiple staff to ensure clinical
  trials are conducted appropriately and within the guidelines.
• Provide training and mentoring of lower-level staff to
  ensure compliance and achievement of enrollment goals.
• Communicate regularly with management to share updates,
  problem-solve, make decisions, etc.

New Study oversight:

• Participate in the design and implementation of new clinical
  trials.
• Assist Investigators with study startup activities.
• Assist regulatory team to create and complete regulatory
  documentation.
• Assist to train and ready team for study startup.
• Implement study activities

Operational Oversight & Regulatory Compliance:

• Ensure regulatory compliance by ensuring all members of
  assigned team have completed required trainings and are aware of operational
  and protocol changes.
• Develop and implement strategies to achieve PI goals for
  participant engagement, enrollment and retention.
• Ensure study teams are documenting all visits accordingly in
  portals such as OnCore, Box, RedCap, etc.
• Ensure staff follow standards of ALCOA and GCP

Knowledge, Skills and Abilities:

• Excellent interpersonal skills.
• Willing to work in a clinical setting.
• Ability to work independently and in a team.
• Ability to maneuver multiple tasks at once.
• Knowledge of Cerner, OnCore, RedCap.

• Bachelor's degree or equivalent advanced learning attained through professional level experience
  required.
• Minimum of 5 years of relevant work experience, or equivalent combination of education and work
  experience.

• Please note: If invited to interview, please be prepared to provide three (3) professional references.