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HomeCompaniesIazuqy Fa Ocs Oraclecloud Com CX 1Clinical Research Coordinator Cardiology

Clinical Research Coordinator Cardiology

Iazuqy Fa Ocs Oraclecloud Com CX 1 · San Francisco, CA, United States; Dolby Regeneration Medicine - FL 09 - RM 903E, San Francisco, CA, US · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyIazuqy Fa Ocs Oraclecloud Com CX 1
TitleClinical Research Coordinator Cardiology
Normalized title-
Department / teamResearch and Laboratory
LocationSan Francisco, CA, United States
Work model-
Employment type-
Salary-
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-03-26 / 2026-05-31
Changed / last seen2026-06-10 / 2026-06-20

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PageWhat it containsOpen
Company jobsActive postings from Iazuqy Fa Ocs Oraclecloud Com CX 1.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Oracle Recruiting Cloud / Fusion HCM.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in San Francisco.Open
Department jobsActive postings in Research and Laboratory.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyIazuqy Fa Ocs Oraclecloud Com CX 1
Source1ec01ec1-9ec0-4ca7-9242-3de42049e519
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description The Department of Medicine, Division of Cardiology, has developed a clinical research infrastructure within the Division. The goals are to increase industry-sponsored research, create a system that supports physicians in operationalizing investigator-initiated studies, and develop a general cardiology cohort study. The purpose of this position is to carry out tasks as part of ongoing and future clinical and translational research projects within the Division of Cardiology. Under the supervision of the Clinical Research Supervisor or Manager, the incumbent will perform duties related to the support and coordination of clinical studies and may receive training and development to prepare for advancement to the next level within the series. Qualifications Required Qualifications: • HS graduate and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities • Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; 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. • Demonstrated ability to exercise tact and discretion in sensitive communications with patients and others. Demonstrated ability in handling a variety of confidential information appropriately. • Demonstrated positive interpersonal skills and problem solving abilities. • Willing to travel (limited travel for investigator meetings) Preferred Qualifications: • Experience in clinical cardiology and clinical/cardiovascular research • Science, research, or medical background • Applied knowledge in drug and/or device trials • A two-year commitment is preferred • Proficiency in the use of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system. • Understanding of patient population to create rapport, while also giving insight to what is realistic and appropriate for patient participation. • In-depth knowledge of ICH/GCP and FDA requirements for INDs, IDEs, and NDAs. • Experience in building strong working relationships with Sponsors, Monitors, PIs, and other key stakeholders • Experience with electronic medical records, EPIC preferred. • Knowledge of biospecimen collection, processing, and transport • Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPAA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms. • Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals • Experience applying the following regulations and guidelines: • Good Clinical Practice Guidelines • Health Information and Accountability Act (HIPAA) • The Protection of Human Research Subjects • CHR regulations for recruitment and consent of research subjects • Effective Cash Handling Procedures • Environmental Health and Safety Training • Fire/ Life Safety Training License / Certification: • No

Full job record

Job ID04921a4394ed01ac7c807a7bbeab462a54f01bc9
Org IDb73f2bf1-b0ab-47ed-8db1-1f14a038aa7c
Source ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Board ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Provideroracle_hcm
Provider Job KeyCONV_87501BR
TitleClinical Research Coordinator Cardiology
Normalized Title
Statusactive
Activeyes
Location TextSan Francisco, CA, United States; Dolby Regeneration Medicine - FL 09 - RM 903E, San Francisco, CA, US
DepartmentResearch and Laboratory
Team
Employment Type
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CountryUnited States
RegionCA
CitySan Francisco
Salary RawDescription The Department of Medicine, Division of Cardiology, has developed a clinical research infrastructure within the Division. The goals are to increase industry-sponsored research, create a system that supports physicians in operationalizing investigator-initiated studies, and develop a general cardiology cohort study. The purpose of this position is to carry out tasks as part of ongoing and future clinical and translational research projects within the Division of Cardiology. Under the supervision of the Clinical Research Supervisor or Manager, the incumbent will perform duties related to the support and coordination of clinical studies and may receive training and development to prepare for advancement to the next level within the series. Qualifications Required Qualifications: • HS graduate and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities • Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; 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. • Demonstrated ability to exercise tact and discretion in sensitive communications with patients and others. Demonstrated ability in handling a variety of confidential information appropriately. • Demonstrated positive interpersonal skills and problem solving abilities. • Willing to travel (limited travel for investigator meetings) Preferred Qualifications: • Experience in clinical cardiology and clinical/cardiovascular research • Science, research, or medical background • Applied knowledge in drug and/or device trials • A two-year commitment is preferred • Proficiency in the use of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system. • Understanding of patient population to create rapport, while also giving insight to what is realistic and appropriate for patient participation. • In-depth knowledge of ICH/GCP and FDA requirements for INDs, IDEs, and NDAs. • Experience in building strong working relationships with Sponsors, Monitors, PIs, and other key stakeholders • Experience with electronic medical records, EPIC preferred. • Knowledge of biospecimen collection, processing, and transport • Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPAA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms. • Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals • Experience applying the following regulations and guidelines: • Good Clinical Practice Guidelines • Health Information and Accountability Act (HIPAA) • The Protection of Human Research Subjects • CHR regulations for recruitment and consent of research subjects • Effective Cash Handling Procedures • Environmental Health and Safety Training • Fire/ Life Safety Training License / Certification: • No
Salary Min
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Source URLhttps://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/CONV_87501BR
Apply URLhttps://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/CONV_87501BR
First Seen At2026-05-31 17:57:33Z
Last Seen At2026-06-20 11:50:40Z
Last Checked At2026-06-20 11:50:40Z
Last Changed At2026-06-10 11:01:18Z
Inactive At
Source Posted At2026-03-26 00:00:00Z
Source Updated At
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Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/04921a4394ed01ac7c807a7bbeab462a54f01bc9?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/b73f2bf1-b0ab-47ed-8db1-1f14a038aa7cJSON
GET https://api.bluedoor.sh/job-postings/v1/sources/1ec01ec1-9ec0-4ca7-9242-3de42049e519JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/04921a4394ed01ac7c807a7bbeab462a54f01bc9/eventsJSON