Clinical Research Coordinator III - Department of Dermatology

• 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.

Knowledge, Skills, and Abilities:

• 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.