Clinical Research Coordinator (Crc)

Job Description Job Description The Clinical Research Coordinator (CRC) is responsible for coordinating and administering clinical trials under the direction of the Principal Investigator. The CRC will develop, implement, and coordinate research and administrative procedures for successfully managing clinical trials.

The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study-specific protocols. DUTIES AND RESPONSIBILITIES Administratively and clinically manage an average of six to eight clinical trials Adhere to Research SOP’s Adhere to Good Clinical Practices and specific study protocols Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials Discuss study protocols with patients and verify the informed consent documentation Provide patient with written communication of their participation (i.e. copy of the signed informed consent) Ensure patient’s referring physician receives notification of patient’s participation in studies as requested by the patient Meet with patient for each visit and maintain accessibility to discuss any questions or concerns regarding the study Dispense study medication in a professional and accountable manner following protocol requirements Collect, process, and ship blood/urine specimens at scheduled patient visits Perform ECGs and obtain vital signs of patients Schedule all patient research visits and procedures consistent with protocol requirements Complete and maintain case report forms per FDA guidelines and review them against the patient’s medical record for completeness and accuracy Administer questionnaires/diaries per protocol Ensure that non-serious and serious adverse events are properly documented and reported Screen all laboratory results when received and follow protocol procedure regarding abnormal results Ensure all laboratory results are given to appropriate doctors for review of clinical significance, then file results in the patient study binder Ensure all regulatory documents are filed and maintained Schedule monitor visits and set up for monitoring visits prior to monitor’s arrival Other duties as assigned. EDUCATION & EXPERIENCE Minimum 4 year college degree required Minimum of two years clinical research coordinator experience required Previous experience with CNS clinical trials highly desirable Phlebotomy, lab processing experienced required QUALIFICATIONS & REQUIREMENTS Able to read, analyze, and interpret information from professional journals, technical procedures, or governmental regulations Able to effectively present information and respond to questions from physicians, staff and patients Knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research required Knowledge of the International Air Transport Association (IATA) regulations for the transportation of Dangerous Goods Phlebotomy, lab processing experienced required Team-oriented and adaptable Demonstrates consistent professional conduct and meticulous attention to detail Possesses excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals Occasional travel required for investigator meetings Company Description Our Mission:

We put people first by providing expert care compassionately, professionally, and ethically. As a team, we work together to provide hope and advancements in medical knowledge and treatment. Our Goal: Dr.

Garcia and his team provide expert care in a compassionate, safe and comfortable clinical setting. With over 30 years clinical experience and 20 years experience in clinical research, Austin Clinical Trial Partners work together with our patients, trial participants and study partners to ensure successful outcomes. Company Description Our Mission:

We put people first by providing expert care compassionately, professionally, and ethically. As a team, we work together to provide hope and advancements in medical knowledge and treatment.

Our Goal:

Dr. Garcia and his team provide expert care in a compassionate, safe and comfortable clinical setting. With over 30 years clinical experience and 20 years experience in clinical research, Austin Clinical Trial Partners work together with our patients, trial participants and study partners to ensure successful outcomes.