Clinical Research Coordinator III - Department of Dermatology
About The Position
The Division of Dermatology in the Department of Medicine is seeking applicants for a Clinical Research Coordinator III to support the establishment and daily operations of a Dermatology clinical trial unit under the oversight of Dr. Daniel C. Butler. This position explores and discovers answers to challenging questions. The Clinical Research Coordinator III develops, facilitates, implements, evaluates, performs, administers and oversees a wide variety of research programs and initiatives within the division with new focus on immunological directed clinical studies. This position implements, maintains, documents, and manages clinical trials and provides for the safety of patients involved in clinical trials ensuring protocol adherence.
Requirements
- Bachelor's degree or equivalent advanced learning attained through professional level experience required.
- Minimum of five (5) years of relevant work experience, or equivalent combination of education and work experience.
- Knowledge of the broad industry best practices, techniques, and standards.
- Excellent record keeping and data entry skills.
- Knowledge of human subjects protection program requirements and regulations.
- Ability to work autonomously and as part of a team.
- Ability to communicate effectively with different groups/individuals.
Nice To Haves
- Experience in dermatology clinical studies in a University setting.
Responsibilities
- Lead the coordination and administration of multiple dermatology clinical trials, contracts, protocols and treatment plans, simultaneously.
- Work in conjunction with the Principal Investigator to design and develop clinical trial protocols.
- Independently prepare, coordinate, and maintain regulatory study documentation including IRB submission and approval of new or revised protocols, safety reports and progress reports.
- Participate in data management design and maintenance.
- Keep appropriate logs, track participants, and prepare study materials.
- Recruit and enroll study participants, interview and evaluate potential participants, obtain consents and explain research protocols to study participants.
- Develop and provide education materials and training to patients, family members, and clinical staff to assure patient safety and adherence to protocols.
- Coordinate and conduct study appointments and procedures, including obtain medical history and vitals, collection of specimens, administering medication; assess and monitor patient's health.
- Conduct adverse event assessment and provide recommendation to PI.
- Ensure proper collection, processing and handling of specimens.
- Develop source documents, Standard Operating Procedures, and study specific training.
- Coordinate and attend sponsor monitor visits.
- Plan and lead work of the two lower level Clinical Research Coordinators this position will be supervising.
- Manage team coordination, communication, training, and quality control.
- Order and maintain supplies and make day-to-day decisions in support of the studies.
Benefits
- health, dental, and vision insurance plans
- life insurance and disability programs
- paid vacation, sick leave, and holidays
- U of A/ASU/NAU tuition reduction for the employee and qualified family members
- retirement plans
- access to U of A recreation and cultural activities
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
