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Work with PIs, under moderate guidance, in coordinating activities related to recruitment for clinical trials including recruitment of study participants, conduct interviews, evaluate potential participants, obtain informed consent, collect and maintain subject data, and perform research subjects' assessment and Neurologic Rating Scales (NIHSS, mRS, MDS-UPDRS, UDysRS, MoCA, C-SSRS, etc).Provide input into the design, development, execution, and initial interpretation of clinical trial protocols, treatment plans, compliance forms, and tracking documents. Conduct research work and perform professional literature reviews to assist the Principal Investigator in designing appropriate research methodologies, techniques, and procedures.Serve as a patient resource for concerns and information. Prepare, coordinate, and/or maintain regulatory documentation including IRB submission and approval of new or revised protocols, safety reports, and progress reports.Collect and submit the required documentation to the Institutional Review Board, the University, and corporate or government sponsors.Participate in data management design and maintenance.Develop administrative and financial recommendations for department management and PIs for research portfolio review. Oversee quarterly review of all Principal Investigator accounts, performing a strategic analysis of PI research portfolios.Collaborate with the Principal Investigator in the preparation of Human Subjects documentation for NIH and other federally funded grant applications.Create and prepare education materials and training to patients, family members, and clinical staff to assure patient safety and adherence to protocols.Administer and assist in the proper collection, processing, storage, and transport of biological specimens and ensure their handling.Order and maintain supplies required for study kits, track spending in this area, and make day-to-day decisions in support of the study.May mentor and train new staff in preparation and conduct of clinical trials.
Knowledge, Skills, and Abilities
Knowledge about neurological disorders including movement disorders (e.g., Parkinson's disease), seizure disorders (e.g., epilepsy syndromes) and vascular neurological disorders.Passion for neurological research and development of treatments for neurological disorders.Motivated to provide high quality, compliant research.Skill in maintaining detailed records.Desire to build new program and develop new policies.Ability to work both independently and with a team, resolving issues with a positive outcome.High level of integrity, ethics, and professionalism.Strong communication and computer skills.Strong organization skills and significant attention to detail for data entry.
Part Time
$64k-84k (estimate)
05/27/2024
06/09/2024
arizona.edu
NOGALES, AZ
15,000 - 50,000
Private
DARCY DIXON
$1B - $3B
Colleges & Universities
The following is the career advancement route for Clinical Research Coordinator II (Part-Time) positions, which can be used as a reference in future career path planning. As a Clinical Research Coordinator II (Part-Time), it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Coordinator II (Part-Time). You can explore the career advancement for a Clinical Research Coordinator II (Part-Time) below and select your interested title to get hiring information.