U

UCSF

Public health sciences university in San Francisco

Clinical Research Coordinator - Surgery

Medical ResearchPosted on Nov 9
Full-timeSan Francisco, CA, USA$40.14 - $64.55In-person

About the Job

Requirements

  • A high school diploma, or equivalent experience or training.
  • Attention to detail, strong interpersonal skills, and effective verbal and written communication skills to multitask in a fast-paced environment with a diverse subject population.
  • Ability to coordinate with subjects, team members, other departments, and outside institutions.
  • Ability to work independently, complete projects on time, and prioritize multiple projects to meet deadlines.

Responsibilities

  • Execute, manage, and coordinate research protocols independently or with general direction, and coordinate data collection and operations for concurrent clinical research studies according to protocols and applicable policies.
  • Support the management and coordination of clinical research studies based on their size and complexity; act as an intermediary between services and departments; oversee data and specimen management; and manage and report study results.
  • Create, clean, update, and manage databases, comprehensive datasets, and reports.
  • Coordinate staff work schedules and assist with training Assistant Clinical Research Coordinators; assist the Clinical Research Supervisor or Principal Investigator with oversight of research staff.
  • Manage investigator protocols in the Committee on Human Research online system, including renewals, modifications, and implementation of new studies; participate in protocol review and writing to support institutional review board approval and compliance.
  • Help assure compliance with applicable regulatory agencies, oversee study data integrity, implement periodic quality control procedures, obtain institutional approval before study initiation, and maintain regulatory documents.
  • Report study progress to investigators and participate in internal and external audits or reviews of study protocols.
  • Identify subjects, develop recruitment and retention strategies, and screen and enroll study subjects.
  • Schedule study visits; administer questionnaires, collect medical histories, and perform study procedures.
  • Maintain rapport with subjects, communicate effectively, respond to diverse needs, schedule follow-up appointments, act as an intermediary, and discuss study outcomes with providers to support continuity of care.
  • Obtain informed consent, review information with subjects, and assess and advocate for patient safety during protocol procedures.
  • Oversee subject reimbursement and resolve discrepancies and issues.
  • Coordinate with staff to complete procedures, properly store specimens, collect required visit data, and ensure correct shipping and labeling.
  • Coordinate and communicate with other studies, technicians, and affiliated groups to improve scheduling efficiency.
  • Review medical charts and electronic records to extract information for studies.
  • Assess needs and recommend enhancements to patient coordination, data collection, data management, protocol adherence, and study collaboration.
  • Enter data from visits, procedures, laboratory tests, and other subject participation into databases promptly.
  • Manage and improve database structures for protocols, create databases as needed, and maintain comprehensive datasets and data collection forms.
  • Query and analyze databases, work with the supervisor to maintain accurate study data, and analyze data as it becomes available.
  • Train staff on protocols, procedural changes, data collection and entry, database procedures, medical chart review and storage, and related procedures; attend and participate in regular team meetings.
  • Assess policies and procedures for subject recruitment, data collection, and data management; maintain procedure manuals and plans for consistent data collection and entry.
  • Modify data collection instruments, schedule staff time, coordinate staff schedules, and maintain subject tracking systems.
  • Arrange specimen exchanges and transport with collaborating investigators and staff; oversee data interpreted from samples and ensure it is used correctly for analysis and publications; maintain sample integrity and security.
  • Design and enhance case report and data collection forms, provide manuscript feedback, and develop systems for protocol adherence and data quality.
  • Renew, modify, and submit Committee on Human Research applications and protocols, track approval status, liaise between the committee and investigators, and evaluate protocols for needed improvements.
  • Conduct studies according to applicable federal regulations, Good Clinical Practice, and institutional regulations; monitor data submission timelines and document and submit adverse events to appropriate departments.
  • Maintain patient confidentiality when communicating with agencies, healthcare providers, other studies, and outside departments; prepare documentation for audits and protocol reviews.

Desired Qualifications

  • Fluency using the Committee on Human Research online iMEDris system to submit, renew, and modify protocols.
  • Understanding of the patient population to build rapport and assess what is realistic and appropriate for patient participation.
  • Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals.
  • A Bachelor of Science degree.
  • Experience with electronic medical records.
  • Knowledge of institutional and departmental policies for reimbursement, research guidelines, confidentiality, and HIPAA; understanding of patient safety and confidentiality procedures for electronic and paper records, charts, and communications.
  • Knowledge of medical terminology, research policies and guidelines, infectious-substance packing and shipping guidelines, database building and analysis, and data management using Access, Stata, SAS, SPSS, or Teleform programming platforms.
  • Experience applying Good Clinical Practice Guidelines, the Health Insurance Portability and Accountability Act, The Protection of Human Research Subjects, Committee on Human Research regulations for recruitment and consent, Effective Cash Handling Procedures, Environmental Health and Safety Training, and Fire Safety Training.

About the Company

UCSF

Public health sciences university in San Francisco

UC San Francisco is a public research university in San Francisco focused solely on health sciences, combining professional education with biomedical research and patient care. Its schools of dentistry, medicine, nursing and pharmacy train clinicians and scientists, while teams investigate cancer, immunology, genomics and neuroscience. UCSF Medical Center and Benioff Children's Hospitals connect clinical care with faculty research and training, and university clinics serve patients across Northern California. Founded in 1864, UCSF is the University of California campus dedicated to graduate and professional education and biomedical research, based in San Francisco.

Company size
10,001+
Company stage
Not listed
Total funding
Not listed
Headquarters
Not listed
Founded
1864

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