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HomeCompaniesEmis Fa Us2 Oraclecloud Com CXDirector - Oncology Research

Director - Oncology Research

Emis Fa Us2 Oraclecloud Com CX · Charlotte, NC, United States; LCI - 1021 Morehead Medical Dr, Charlotte, NC, US · Active · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyEmis Fa Us2 Oraclecloud Com CX
TitleDirector - Oncology Research
Normalized title-
Department / teamDirector/AVP (Dept Head)
LocationCharlotte, NC, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2025-04-25 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-18

Related slices

PageWhat it containsOpen
Company jobsActive postings from Emis Fa Us2 Oraclecloud Com CX.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 Charlotte.Open
Department jobsActive postings in Director/AVP (Dept Head).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

CompanyEmis Fa Us2 Oraclecloud Com CX
Sourced920bfc9-0080-481b-907d-77f64777489f
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description Job Summary A senior member of the clinical trials leadership team that provides strategic direction, develops and communicates vision for the department, shares expertise across multiple discipline, creates an environment of continuous improvement by defining business needs and driving transformational change, sponsors and leads innovative projects and uses project management methodologies to position LCI for success, helps develop and lead enterprise strategy through programmatic, geographic, technical and operational assessments and planning. Essential Functions Demonstrates expert knowledge of Good Clinical Practices (GCP), International Conference on Harmonization (ICH) Guidelines, as well as applicable rules/regulations pertaining to research. Knowledge of regulatory requirements of the Food and Drug Administration (FDA), Institutional Review Board (IRB), and Office of Human Subjects Protections (OHRP) pertaining to clinical research. Assists in developing the operational budget for the LCI Clinical Trials Department Provides strategic direction and oversight for clinical trial projects which are enterprise-wide and assists with strategic planning for both the enterprise-wide growth of clinical trials and associated operations. Performs metric analysis to ensure research workload for clinical trial operations meets the overall research team objectives. Responsible for comprehensive Time and Effort reporting requirements to Research Finance ensuring research time is allocated appropriately. Ensures all clinical trial operations are in compliance with ICH, GCP and FDA requirements. Ensures appropriate documentation is maintained to meet applicable federal regulatory requirements as well as trial sponsor requirements. Ensures the department is prepared for sponsor and governmental audits and inspections. Provides updates to executive stakeholders on current/forecasted resource requirements, accrual status, financial performance, investigator performance, etc. through formal presentations and reports. Develops and monitors performance reports related to the trials portfolio (includes sponsor and CRO reports, corporate financial performance, corporate HR reports, CTMS-based reports, key performance indicators, etc.). Physical Requirements Primarily works in an office setting. Requires full range of body motion; sitting for extensive periods of time; walking, standing, reading, and writing/keyboarding. Occasionally lifts and carries items weighing up to 35 pounds. Requires corrected vision and hearing within normal range. Must speak and read/write clearly in English. Must be able to be mobile within the entire healthcare system and other locations that participate in LCI clinical trials. Education, Experience and Certifications Bachelor's Degree required, health/science preferred. Minimum of 15 years of directly-related clinical trials experience with a pharmaceutical company, Contract Research Organization (CRO), research center or equivalent required; management experience required; oncology experience required. RN not required, however RNs must hold a current NC Board of Nursing license and current CPR certification. Or Master’s Degree with at least 10 years of directly-related clinical trials experience with a pharmaceutical company, Contract Research Organization (CRO), research center or equivalent required; management experience required; oncology experience required. RN not required, however RNs must hold a current NC Board of Nursing license and current CPR certification. In addition to either of the above, previous experience in a healthcare setting required, especially in a cancer and/or cancer research environment. Certification in clinical research (SoCRA CCRP, ACRP, RAPS, or similar) preferred.

Full job record

Job ID46363de885386a1cb912fe80244ba2ab43fc7309
Org ID553bf120-c221-4e6d-8c9a-de9c030b187c
Source IDd920bfc9-0080-481b-907d-77f64777489f
Board IDd920bfc9-0080-481b-907d-77f64777489f
Provideroracle_hcm
Provider Job Key151741
TitleDirector - Oncology Research
Normalized Title
Statusactive
Activeyes
Location TextCharlotte, NC, United States; LCI - 1021 Morehead Medical Dr, Charlotte, NC, US
DepartmentDirector/AVP (Dept Head)
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
RegionNC
CityCharlotte
Salary RawDescription Job Summary A senior member of the clinical trials leadership team that provides strategic direction, develops and communicates vision for the department, shares expertise across multiple discipline, creates an environment of continuous improvement by defining business needs and driving transformational change, sponsors and leads innovative projects and uses project management methodologies to position LCI for success, helps develop and lead enterprise strategy through programmatic, geographic, technical and operational assessments and planning. Essential Functions Demonstrates expert knowledge of Good Clinical Practices (GCP), International Conference on Harmonization (ICH) Guidelines, as well as applicable rules/regulations pertaining to research. Knowledge of regulatory requirements of the Food and Drug Administration (FDA), Institutional Review Board (IRB), and Office of Human Subjects Protections (OHRP) pertaining to clinical research. Assists in developing the operational budget for the LCI Clinical Trials Department Provides strategic direction and oversight for clinical trial projects which are enterprise-wide and assists with strategic planning for both the enterprise-wide growth of clinical trials and associated operations. Performs metric analysis to ensure research workload for clinical trial operations meets the overall research team objectives. Responsible for comprehensive Time and Effort reporting requirements to Research Finance ensuring research time is allocated appropriately. Ensures all clinical trial operations are in compliance with ICH, GCP and FDA requirements. Ensures appropriate documentation is maintained to meet applicable federal regulatory requirements as well as trial sponsor requirements. Ensures the department is prepared for sponsor and governmental audits and inspections. Provides updates to executive stakeholders on current/forecasted resource requirements, accrual status, financial performance, investigator performance, etc. through formal presentations and reports. Develops and monitors performance reports related to the trials portfolio (includes sponsor and CRO reports, corporate financial performance, corporate HR reports, CTMS-based reports, key performance indicators, etc.). Physical Requirements Primarily works in an office setting. Requires full range of body motion; sitting for extensive periods of time; walking, standing, reading, and writing/keyboarding. Occasionally lifts and carries items weighing up to 35 pounds. Requires corrected vision and hearing within normal range. Must speak and read/write clearly in English. Must be able to be mobile within the entire healthcare system and other locations that participate in LCI clinical trials. Education, Experience and Certifications Bachelor's Degree required, health/science preferred. Minimum of 15 years of directly-related clinical trials experience with a pharmaceutical company, Contract Research Organization (CRO), research center or equivalent required; management experience required; oncology experience required. RN not required, however RNs must hold a current NC Board of Nursing license and current CPR certification. Or Master’s Degree with at least 10 years of directly-related clinical trials experience with a pharmaceutical company, Contract Research Organization (CRO), research center or equivalent required; management experience required; oncology experience required. RN not required, however RNs must hold a current NC Board of Nursing license and current CPR certification. In addition to either of the above, previous experience in a healthcare setting required, especially in a cancer and/or cancer research environment. Certification in clinical research (SoCRA CCRP, ACRP, RAPS, or similar) preferred.
Salary Min
Salary Max
Salary Currency
Salary Periodhour
Source URLhttps://emis.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX/job/151741
Apply URLhttps://emis.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX/job/151741
First Seen At2026-05-31 18:13:59Z
Last Seen At2026-06-18 12:01:22Z
Last Checked At2026-06-18 12:01:22Z
Last Changed At2026-05-31 18:13:59Z
Inactive At
Source Posted At2025-04-25 20:16:44Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=emis.fa.us2.oraclecloud.com|CX/date=2026-06-18/2026-06-18T12-00-42-546Z-79d0d4c0368a8a203a6a886236054027e778e6ad7a75cf54f56f5b4e666704ac.json
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