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Clinical Research Coordinator Sudden Cardiac Death Study

Job in San Francisco, San Francisco County, California, 94199, USA
Listing for: University of California - San Francisco Campus and Health
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
  • Research/Development
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 150000 - 200000 USD Yearly USD 150000.00 200000.00 YEAR
Job Description & How to Apply Below

Clinical Research Coordinator Sudden Cardiac Death Study

MED-CORE-CARD

Full Time

86632

Job Summary

The Clinical Research Coordinator (CRC) will execute, manage, and coordinate the routine duties of the POstmortem Inves Tigation of Sudden Cardiac Death (POST SCD) research program alongside a team of CRCs under the guidance of the Principal Investigator (PI) and/or study team. Learn more about the lab here, (Use the "Apply for this Job" box below). POST SCD is a clinical research laboratory with a multidisciplinary team and collaborations with local and federal agencies to comprehensively characterize the burden, underlying causes, and risk factors of sudden cardiac death (SCD) in our prototypic, diverse U.S. community.

It is a first of its kind partnership between cardiac electrophysiology specialists and the County Medical Examiner to perform comprehensive autopsies and antemortem medical history review for every incident out-of-hospital sudden death within the County of San Francisco.

  • Support the management and coordinate the tasks of multiple clinical research studies;
  • Act as intermediary between research team and collaborators while overseeing data and specimen management;
  • Manage and report on study results;
  • Create, clean, update, and manage databases and comprehensive datasets and reports;
  • Manage Investigator's protocols in the Committee on Human Research online system, renewals and modifications of protocol applications and the implementation of new studies;
  • Participate in the review and writing of protocols to ensure institutional review board approval within University compliance;
  • Help assure compliance with all relevant regulatory agencies;
  • Oversee study data integrity;
  • Implement and maintain periodic quality control procedures;
  • Interface with departments to obtain UCSF approval prior to study initiation;
  • Maintain all regulatory documents;
  • Report study progress to investigators;
  • Participate in any internal and external audits or reviews of study protocols;
  • Perform other duties as assigned.

Your placement within the salary range is subject to additional approvals based on UC policy. The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification  positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.

The salary range for this position is $37.12 - $59.69 (Hourly Rate).

To learn more about the benefits of working at UCSF, including total compensation, please visit: .html

Department Description

POST SCD is a clinical research laboratory with a multidisciplinary team and collaborations with local and federal agencies to comprehensively characterize the burden, underlying causes, and risk factors of sudden cardiac death (SCD) in our prototypic, diverse U.S. community. It is a first of its kind partnership between cardiac electrophysiology specialists and the County Medical Examiner to perform comprehensive autopsies and antemortem medical history review for every incident out-of-hospital sudden death within the County of San Francisco.

Learn more about the lab here, .

Required Qualifications
  • HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training
  • Attention to detail; articulate; self-motivated; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with study subjects, team members, other departments and outside collaborators; and the ability to multi-task in a fast-paced environment while working with a diverse subject population.
  • Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines.
  • Previous research experience and demonstrated skills to successfully perform the…
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