Coordinate clinical data entry and management for Caris Precision Oncology Alliance sites, ensuring data integrity and compliance with GCP and regulatory standards.
The CRC is responsible for coordinating and assuring integrity of all activities associated with conducting TBICoE clinical investigations in the area of TBI, ensuring compliance with local, state, and federal regulatory requirements.
Compensation
The likely salary range for this position is $57,824 - $78,200.
Responsibilities
Coordinates and assures integrity of all activities associated with conducting TBICoE TBI clinical investigations
Assists Principal / Associate Investigators in the preparation and submission of clinical protocols, consent forms, and other documents
Maintains regulatory files related to TBICoE clinical investigations
Communicates with research participants, staff, regulatory affairs and data management groups, laboratory and clinical investigators
Recruits, interviews, and screens TBICoE clinical research study volunteers, administers and obtains informed consent
Requirements
Bachelor's degree or higher in biology, psychology or related science
Nice to have: Master’s degree
Nice to have: Certification as a Clinical Research Coordinator (CCRC)
Nice to have: Clinical Research Professional (CCRP)
The Clinical Research Coordinator 2 (CRC2) supports and coordinates daily clinical trial activities, managing enrollment, data collection, and regulatory compliance.
Compensation
$60,000.00 - $75,000.00
Responsibilities
Manages all aspects of conducting clinical trials including screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.
Recruits and interviews potential study patients with guidance from PI and other clinical research staff.
Collects, processes, ships and stores specimens to appropriate laboratory according to established aseptic techniques.
Identifies and explains the responsibilities of principal investigators, research team members, sponsors, contract research organizations (CROs), and regulatory authorities related to the conduct of a clinical trial.
Coordinates the conduct of the study from startup through closeout including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence.
Administers specialized diagnostic tests in Audiology
Operates Hearing Aid Dispensary and Cochlear Implant Center
Manages budget, CI program development, research, philanthropy, outreach and marketing
Oversees operation of the Cochlear Implant Center including protocol development, coding, billing, evaluation and management of cochlear implant recipients
Coordinates audiometric results with other diagnostic data and makes recommendations
Oversee all aspects of data operations for the Perinatal Research Program (PRP), ensuring data integrity, security, compliance, and operational excellence.
Responsibilities
Independently manage research data across multiple PRP research studies, ensuring data integrity, security, and compliance with institutional, sponsor, and regulatory requirements.
Design, develop, implement, and maintain research databases, data dictionaries, data collection instruments, study protocols, and manuals of operations.
Establish standardized data management procedures to ensure consistency across multiple recruitment and collaborating sites.
Develop and maintain comprehensive documentation for all data management processes, including standard operating procedures (SOPs), data dictionaries, and version control.
Extract, transform, validate, clean, and prepare complex datasets for statistical analysis and reporting.
Requirements
Bachelor's degree in related area or equivalent experience
Provide direct clinical and data management support for Yale Cancer Center clinical trials, including data abstraction, record maintenance, and reporting.
Compensation
$31.83
Responsibilities
Researches and collects data through site or home visit intakes; library research; structured interviews; or other means for research projects.
Interprets, synthesizes, and analyzes data using scientific or statistical techniques.
Modifies and plans research experiments, procedures, tests, or survey instruments.
Assists in research design.
Writes and edits material for publication and presentation.
Data and Analytics ManagerUCSF · San Francisco, US