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Clinical Research Supervisor

Iazuqy Fa Ocs Oraclecloud Com CX 1 · San Francisco, CA, United States; 1 Shrader Street - FL 04 - RM 428, San Francisco, CA, US · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyIazuqy Fa Ocs Oraclecloud Com CX 1
TitleClinical Research Supervisor
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 seen2026-03-29 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-20

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Linked records

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

Description

Description Job Summary : The position of Advanced Lung Disease Clinical Research Supervisor is responsible for the overall operational management of the UCSF Advanced Lung Disease Program’s clinical research activities. Both of these programs are growing substantially and have significant management responsibilities. This position is critically important to the management of the increased clinical research activities. The position of Advanced Lung Disease Clinical Research Supervisor involves direct responsibility for implementing a diverse portfolio of research activities including multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and programmatic clinical research activities such as the clinical database, and biorepository. The Clinical Research Supervisor is a critical position that requires expert and efficient integration of multiple complex programmatic activities. The position requires substantial leadership skills, the ability to effectively work with multiple different people and organizations at UCSF (clinicians, investigators, clinical staff, administration, committee on human research, human resources, contracts and grants) and elsewhere (industry sponsors, coordinating centers, FDA, NIH), and an in depth knowledge of all aspects of the advanced lung disease programs. Under the direction of the Director, ILD Program and the Director of Clinical Trials, ILD Program, the Clinical Research Supervisor will have central responsibility for ensuring CHR approval and compliance, contract generation, negotiation and approval, subject recruitment, appropriate study testing, and adequate enrollment of all multicenter clinical trials, longitudinal cohort studies, local investigator-initiated studies, and biorepository efforts. The Advanced Lung Disease Programs need strong administrative and management leadership, strong research coordination, and experienced personnel who can ensure optimal efficiency, compliance, safety, employee supervision and management, financial oversight, and contractual expertise. This position is a position of leadership whose main purpose is to ensure that the programs’ clinical research commitments are met and that the program maintains excellence in all its activities. Qualifications Required Qualifications : Bachelor’s degree in related and five or more years of related experience which includes three or more years of supervisory experience and / or an equivalent combination of education and experience. At least 3 years experience in clinical trial management or equivalent years progressively responsible experience in a related position including regulatory and compliance responsibilities. Three to 5 years in a Lead or Supervisory role. Clinical Trial Professional certification from a professional society within one year in position. Experience serving as a project manager and the ability to develop project plans and schedules and to motivate team members to complete objectives within deadlines. Demonstrated experience in audit preparation, execution, and follow-up. Experience using database software, such as MS Access or Filemaker Pro. Experience with UCSF grant application procedures, personnel documentation and contracts generation, and CARE and UCSF subcontracting. Demonstrated ability to develop recruitment strategies in complex environments and differing patient pools, independently identifying recruitment leads, implementing new strategies and continually adjusting strategies to meet recruitment goals as needed. In-depth and extensive knowledge of clinical research contracts and grants, clinical trials, protocols, FDA regulations, and complex visit structures. Project management skills in order to oversee the administrative operations of the clinical trials program. Specifically, s/he must have knowledge of strategies for recruiting human subjects to research studies as well as skills for HR management and financial analysis Demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets. Demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets. Fluency in spreadsheet software and the ability to develop independently complex spreadsheets A well-rounded knowledge of human resource management. Previous experience in risk management regarding complicated study subjects, and federal and non-federal sponsors and regulating bodies. Ability to analyze complex and non-routine issues requiring innovative solutions Ability to operate effectively in a changing organizational and technological environment Ability to assess and respond to audit risk. Ability to interpret and apply policies and regulations. Preferred Qualifications : Master’s degree related scientific/medical area. Certified Clinical Research Coordinator License / Certification : Yes License/Certification : Clinical Trial Professional certification from a professional society within one year in position.

Full job record

Job ID715e2810d30ad3c49472b1e3143d65420e189b89
Org IDb73f2bf1-b0ab-47ed-8db1-1f14a038aa7c
Source ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Board ID1ec01ec1-9ec0-4ca7-9242-3de42049e519
Provideroracle_hcm
Provider Job KeyCONV_87624BR
TitleClinical Research Supervisor
Normalized Title—
Statusactive
Activeyes
Location TextSan Francisco, CA, United States; 1 Shrader Street - FL 04 - RM 428, San Francisco, CA, US
DepartmentResearch and Laboratory
Team—
Employment Type—
Workplace Type—
Remote Policy—
CountryUnited States
RegionCA
CitySan Francisco
Salary RawDescription Job Summary : The position of Advanced Lung Disease Clinical Research Supervisor is responsible for the overall operational management of the UCSF Advanced Lung Disease Program’s clinical research activities. Both of these programs are growing substantially and have significant management responsibilities. This position is critically important to the management of the increased clinical research activities. The position of Advanced Lung Disease Clinical Research Supervisor involves direct responsibility for implementing a diverse portfolio of research activities including multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and programmatic clinical research activities such as the clinical database, and biorepository. The Clinical Research Supervisor is a critical position that requires expert and efficient integration of multiple complex programmatic activities. The position requires substantial leadership skills, the ability to effectively work with multiple different people and organizations at UCSF (clinicians, investigators, clinical staff, administration, committee on human research, human resources, contracts and grants) and elsewhere (industry sponsors, coordinating centers, FDA, NIH), and an in depth knowledge of all aspects of the advanced lung disease programs. Under the direction of the Director, ILD Program and the Director of Clinical Trials, ILD Program, the Clinical Research Supervisor will have central responsibility for ensuring CHR approval and compliance, contract generation, negotiation and approval, subject recruitment, appropriate study testing, and adequate enrollment of all multicenter clinical trials, longitudinal cohort studies, local investigator-initiated studies, and biorepository efforts. The Advanced Lung Disease Programs need strong administrative and management leadership, strong research coordination, and experienced personnel who can ensure optimal efficiency, compliance, safety, employee supervision and management, financial oversight, and contractual expertise. This position is a position of leadership whose main purpose is to ensure that the programs’ clinical research commitments are met and that the program maintains excellence in all its activities. Qualifications Required Qualifications : Bachelor’s degree in related and five or more years of related experience which includes three or more years of supervisory experience and / or an equivalent combination of education and experience. At least 3 years experience in clinical trial management or equivalent years progressively responsible experience in a related position including regulatory and compliance responsibilities. Three to 5 years in a Lead or Supervisory role. Clinical Trial Professional certification from a professional society within one year in position. Experience serving as a project manager and the ability to develop project plans and schedules and to motivate team members to complete objectives within deadlines. Demonstrated experience in audit preparation, execution, and follow-up. Experience using database software, such as MS Access or Filemaker Pro. Experience with UCSF grant application procedures, personnel documentation and contracts generation, and CARE and UCSF subcontracting. Demonstrated ability to develop recruitment strategies in complex environments and differing patient pools, independently identifying recruitment leads, implementing new strategies and continually adjusting strategies to meet recruitment goals as needed. In-depth and extensive knowledge of clinical research contracts and grants, clinical trials, protocols, FDA regulations, and complex visit structures. Project management skills in order to oversee the administrative operations of the clinical trials program. Specifically, s/he must have knowledge of strategies for recruiting human subjects to research studies as well as skills for HR management and financial analysis Demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets. Demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets. Fluency in spreadsheet software and the ability to develop independently complex spreadsheets A well-rounded knowledge of human resource management. Previous experience in risk management regarding complicated study subjects, and federal and non-federal sponsors and regulating bodies. Ability to analyze complex and non-routine issues requiring innovative solutions Ability to operate effectively in a changing organizational and technological environment Ability to assess and respond to audit risk. Ability to interpret and apply policies and regulations. Preferred Qualifications : Master’s degree related scientific/medical area. Certified Clinical Research Coordinator License / Certification : Yes License/Certification : Clinical Trial Professional certification from a professional society within one year in position.
Salary Min—
Salary Max—
Salary Currency—
Salary Periodhour
Source URLhttps://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/CONV_87624BR
Apply URLhttps://iazuqy.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/CONV_87624BR
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 At2026-05-31 17:57:33Z
Inactive At—
Source Posted At2026-03-29 00:00:00Z
Source Updated At—
Raw Payload Uris3://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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line-height: normal;\">Project management skills in order to oversee the administrative operations of the clinical trials program.&nbsp; Specifically, s/he must have knowledge of strategies for recruiting human subjects to research studies as well as skills for HR management and financial analysis</span></span></li><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: normal;\">Demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets.</span></span></li><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: normal;\">Demonstrated skills in preparing and presenting financial and quantitative analyses, including financial projections and budgets.</span></span></li><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: normal;\">Fluency in spreadsheet software and the ability to develop independently complex spreadsheets</span></span></li><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: normal;\">A well-rounded knowledge of human resource management.</span></span></li><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: normal;\">Previous experience in risk management regarding complicated study subjects, and federal and non-federal sponsors and regulating bodies.</span></span></li><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: normal;\">Ability to analyze complex and non-routine issues requiring innovative solutions</span></span></li><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: normal;\">Ability to operate effectively in a changing organizational and technological environment</span></span></li><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: normal;\">Ability to assess and respond to audit risk.</span></span></li><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: normal;\">Ability to interpret and apply policies and regulations.</span></span></li></ul></td></tr></tbody></table></figure></div><div class=\"questionContainer fontSize1\" questiontype=\"Custom\" name=\"129349\"><figure class=\"table\"><table><tbody><tr><td><span class=\"questionLabel\">Preferred Qualifications :</span></td></tr></tbody></table></figure><figure class=\"table\"><table><tbody><tr><td><ul style=\"margin-bottom: 11px;\"><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: 107%;\">Master’s degree related scientific/medical area.</span></span></li><li style=\"margin-bottom: 11px;\"><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: 107%;\">Certified Clinical Research Coordinator</span></span></li></ul></td></tr></tbody></table></figure></div><div class=\"questionContainer fontSize1\" questiontype=\"Custom\" name=\"129304\"><figure class=\"table\"><table><tbody><tr><td><span class=\"questionLabel\">License / Certification :</span></td></tr></tbody></table></figure><figure class=\"table\"><table><tbody><tr><td><span class=\"questionInput\" qbchildren=\"@129303\">Yes</span></td></tr></tbody></table></figure></div><div class=\"questionContainer fontSize1\" questiontype=\"Custom\" name=\"129303\"><figure class=\"table\"><table><tbody><tr><td><span class=\"questionLabel\">License/Certification :</span></td></tr></tbody></table></figure><figure class=\"table\"><table><tbody><tr><td><ul><li><span style=\"font-family: Arial, Helvetica, sans-serif;\"><span class=\"questionInput\" qbchildren=\"\" style=\"font-size: 13px; line-height: normal;\">Clinical Trial Professional certification from a professional society within one year in position.</span></span></li></ul></td></tr></tbody></table></figure></div>",
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