Clinical Research Coordinator Parkinson's Research Centers of America - Palo Alto Palo Alto, CA Job Details Full-time $42,500 - $70,000 a year 1 day ago Benefits Health insurance Dental insurance Paid time off Vision insurance Qualifications Vascular access Bachelor of Science Filing Schedule management Clinical data entry Quality data entry FDA regulations Full Job Description Immediate full-time opening for Clinical Research Coordinator at nationally recognized independent Parkinson's Clinical Research Center. Salary based on qualifications and experience. Benefits available. Full-time. Will train motivated new BS graduate. Are you an enthusiastic and inquisitive problem solver, with passion for discovery and helping patients with Parkinson's and other related neurological diseases? Come join our clinical research center team! www.

ParkinsonsCenter.org The Clinical Research Coordinator conducts research activities under the Principal / Sub- Investigator, following all federal regulations and Good Clinical Practice guidelines. Responsible for orchestrating all activities involving the recruitment and enrollment of study patients and managing the critical study documentation and data collection necessary for each protocol. Full-time, onsite position.

Specific CRC Responsibilities and Expectations:

Review the inclusion/exclusion criteria, overall structure, and requirements of each protocol. Recruit, screen and enroll study subjects ensuring compliance with enrollment criteria and facilitate completion of the informed consent document. Perform and/or schedule various study implementation methods and procedures based on protocol and coordinates various clinical activities between departments and other clinical specialists. Maintain source documentation for all data submitted, including clinic or MD visit chart notes, lab data, and procedure reports. Must be proficient in or learn EDC Data Capture and upkeep, that is entering data and resolving queries. Must be skilled in or willing to learn phlebotomy / venipuncture procedures (or willing to learn) and processing laboratory specimens for shipment to central laboratory. Ensure processing and shipping of any specimens to sponsors or central labs according to guidelines of protocol and maintain shipping log. Handle organizational management of all aspects of a trial. Make decisions and use independent judgment. Facilitate Sponsor and/or FDA audits by ensuring that all required documentation is completed, appropriately filed and made available to auditors. Perform technical and professional clinical procedures. Assess subject's responses to interventions/procedures and report any adverse events (AEs) or serious adverse events (SAEs) within regulatory requirements for reporting. Other duties as delegated.

Job Type:

Full-time Pay:

$42,500.00 - $70,000.00 per year

Benefits:

Dental insurance Health insurance Paid time off Vision insurance

Work Location:

In person