The Thoracic Data Management department in the Clinical Trials Office is looking for a Clinical Trials Coordinator I.  

Position Highlights:

• Will serve as the centralized point of contact for communication regarding clinical trials in the start-up process.
• Facilitates the execution of opening clinical trials to accrual within the designated program patient population.
• Communicates protocol specific information to primary clinical trial coordinator and principle investigator during the start-up phase of the protocol.
• Will work with general guidance from supervisor to implement clinical trials through pre-site selection, SRC review, IRB approval, collaboration with ancillary departments, creation of protocol orders and other source documentations and finally SIV and protocol activation.

Ideal Candidate:

• Will have in-depth knowledge of good clinical practices as set forth by Federal regulations.
• Previous coordinator experience, oncology background preferred.
• Engaged, organized individual with strong critical thinking skills who has the ability to work efficiently under pressure.
• Highly motivated, shows initiative, is proactive and able to work independently as well as in a team.

Responsibilities:

• Coordinate clinical research protocols throughout the start-up phase of the trial
• Work collaboratively with specific departments to help maintain appropriate documents.
• Verify the accuracy and completion of documentation including but not limited to, subject eligibility checklist, source documentations, drug dispensing logs, subject screening logs, and study-related communication. 
• Will interact directly with patients, study sponsors, managers and other department personnel.

Credentials and Qualifications:

• Minimum high school diploma with eight (8) years of relevant clinical research experience required OR Associates degree with four (4) years of relevant clinical research experience required.  
• Bachelor's degree preferred