Home › Companies › Iazuqy Fa Ocs Oraclecloud Com CX 1 › Clinical 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
| Field | Value |
|---|---|
| Company | Iazuqy Fa Ocs Oraclecloud Com CX 1 |
| Title | Clinical Research Coordinator Cardiology |
| Normalized title | - |
| Department / team | Research and Laboratory |
| Location | San Francisco, CA, United States |
| Work model | - |
| Employment type | - |
| Salary | - |
| Status | active |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
| Posted / first seen | 2026-03-26 / 2026-05-31 |
| Changed / last seen | 2026-06-10 / 2026-06-20 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Iazuqy Fa Ocs Oraclecloud Com CX 1. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Oracle Recruiting Cloud / Fusion HCM. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in San Francisco. | Open |
| Department jobs | Active postings in Research and Laboratory. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Iazuqy Fa Ocs Oraclecloud Com CX 1 |
| Source | 1ec01ec1-9ec0-4ca7-9242-3de42049e519 |
| ATS provider | Oracle 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 ID | 04921a4394ed01ac7c807a7bbeab462a54f01bc9 |
| Org ID | b73f2bf1-b0ab-47ed-8db1-1f14a038aa7c |
| Source ID | 1ec01ec1-9ec0-4ca7-9242-3de42049e519 |
| Board ID | 1ec01ec1-9ec0-4ca7-9242-3de42049e519 |
| Provider | oracle_hcm |
| Provider Job Key | CONV_87501BR |
| Title | Clinical Research Coordinator Cardiology |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | San Francisco, CA, United States; Dolby Regeneration Medicine - FL 09 - RM 903E, San Francisco, CA, US |
| Department | Research and Laboratory |
| Team | — |
| Employment Type | — |
| Workplace Type | — |
| Remote Policy | — |
| Country | United States |
| Region | CA |
| City | San Francisco |
| Salary Raw | 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 |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/CONV_87501BR |
| Apply URL | https://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/CONV_87501BR |
| First Seen At | 2026-05-31 17:57:33Z |
| Last Seen At | 2026-06-20 11:50:40Z |
| Last Checked At | 2026-06-20 11:50:40Z |
| Last Changed At | 2026-06-10 11:01:18Z |
| Inactive At | — |
| Source Posted At | 2026-03-26 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=iazuqy.fa.ocs.oraclecloud.com|CX_1/date=2026-06-20/2026-06-20T11-48-53-977Z-50889524454c53dbf7cf6d6d324f932d9168eb178c98ec50e1aa8c82b028ac27.json |
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}Get this page with API
Rendered from the bluedoor Job Postings API. Reproduce it:
GET https://api.bluedoor.sh/job-postings/v1/jobs/04921a4394ed01ac7c807a7bbeab462a54f01bc9?include=descriptionJSONGET https://api.bluedoor.sh/job-postings/v1/orgs/b73f2bf1-b0ab-47ed-8db1-1f14a038aa7cJSONGET https://api.bluedoor.sh/job-postings/v1/sources/1ec01ec1-9ec0-4ca7-9242-3de42049e519JSONGET https://api.bluedoor.sh/job-postings/v1/jobs/04921a4394ed01ac7c807a7bbeab462a54f01bc9/eventsJSON