Atrium Health
Oncology Research Specialist - RN
Atrium Health, Charlotte, North Carolina, United States, 28245
Overview
Join to apply for the
Oncology Research Specialist - RN
role at
Atrium Health Department: 80096 Carolinas Medical Center - LC: Clinical Trials: Morehead Status: Full time • Benefits Eligible: Yes • Hours Per Week: 40 • Schedule Details/Additional Information: M-F 8-4 Preferred Candidate Has Research Experience. This is a grant-funded position. Pay Range: $37.50 - $56.25
Essential Functions
Competently fulfills the job responsibilities of the Oncology Research Specialist, and:
Coordinates clinical and regulatory document submissions for clinical trial start-up, consent development and amendment, protocol amendment, continuing review, closure to accrual, action letter, suspension, termination and other reportable regulatory information.
Assesses patient eligibility through chart reviews and patient/family interviews.
Assists in providing patient education regarding the nature of their disease and the benefits/risks of participating in a clinical drug trial.
Collaborates with regulatory team, Principal Investigator, Sub-Investigators, study personnel, IRB, sponsor/CRO/monitor and other internal/external customers to efficiently coordinate documentation/submissions. Conducts routine NCI research base/sponsor website reviews to identify regulatory updates and actions required.
Presents and obtains patient informed consent.
Coordinates accurate data collection and record keeping by reviewing documents and processes for quality assurance.
Ensures timely and accurate submission of data.
Coordinates and prepares for internal and external audits.
Participates in sponsor study start-up and follow-up meetings as appropriate.
Develops study calendars.
Collaborates on billing and financial activity with Research Finance (budgets and billing compliance).
Coordinates scheduling of patient visits, labs, and diagnostic procedures across LCI locations.
Coordinates drug shipments, storage, and accountability with IDS/Pharmacy.
Assists in the development, improvement and review of Standard Operating Procedures and processes.
Provides educational and technical assistance to research staff including orientation and mentoring of new research staff.
Collaborates and participates with teams across the LCI enterprise in a professional and courteous manner.
Interacts professionally with patients and families.
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 Must hold a valid applicable state or South Carolina (as applicable) Board of Nursing license. Bachelor’s Degree (BS) and 1 year of clinical research experience with a pharmaceutical company or Contract Research Organization (CRO) or equivalent experience required; or Master’s Degree (MS) and 0-1 year of clinical research experience with a pharmaceutical company or Contract Research Organization (CRO) or equivalent experience required; or a minimum of 3 years clinical research experience with a pharmaceutical company or Contract Research Organization (CRO) or equivalent experience required with no degree. Bachelor’s Degree in Nursing (BSN) or Master’s Degree in Nursing (MSN) or other health/science degree concentration preferred. CPR certification required. Previous experience in a healthcare setting preferred, especially cancer care and/or clinical research. Certification in clinical research (SoCRA, ACRP, RAPS, etc.) preferred.
Our Commitment to You Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including:
Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training
Premium pay such as shift, on call, and more based on a teammate's job
Incentive pay for select positions
Opportunity for annual increases based on performance
Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program
About Advocate Health Advocate Health is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Advocate Health provides care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin. It employs teammates across hospitals and care locations and participates in hundreds of clinical trials and research studies.
Coordinates the clinical, regulatory, business, and other research-related activities and documentation for clinical trials conducted by the Levine Cancer Institute, following industry standards and applicable regulations including FDA/OHRP guidances, GCP and ICH.
Seniority level
Entry level
Employment type
Full-time
Job function
Health Care Provider
Industries: Hospitals and Health Care
#J-18808-Ljbffr
Join to apply for the
Oncology Research Specialist - RN
role at
Atrium Health Department: 80096 Carolinas Medical Center - LC: Clinical Trials: Morehead Status: Full time • Benefits Eligible: Yes • Hours Per Week: 40 • Schedule Details/Additional Information: M-F 8-4 Preferred Candidate Has Research Experience. This is a grant-funded position. Pay Range: $37.50 - $56.25
Essential Functions
Competently fulfills the job responsibilities of the Oncology Research Specialist, and:
Coordinates clinical and regulatory document submissions for clinical trial start-up, consent development and amendment, protocol amendment, continuing review, closure to accrual, action letter, suspension, termination and other reportable regulatory information.
Assesses patient eligibility through chart reviews and patient/family interviews.
Assists in providing patient education regarding the nature of their disease and the benefits/risks of participating in a clinical drug trial.
Collaborates with regulatory team, Principal Investigator, Sub-Investigators, study personnel, IRB, sponsor/CRO/monitor and other internal/external customers to efficiently coordinate documentation/submissions. Conducts routine NCI research base/sponsor website reviews to identify regulatory updates and actions required.
Presents and obtains patient informed consent.
Coordinates accurate data collection and record keeping by reviewing documents and processes for quality assurance.
Ensures timely and accurate submission of data.
Coordinates and prepares for internal and external audits.
Participates in sponsor study start-up and follow-up meetings as appropriate.
Develops study calendars.
Collaborates on billing and financial activity with Research Finance (budgets and billing compliance).
Coordinates scheduling of patient visits, labs, and diagnostic procedures across LCI locations.
Coordinates drug shipments, storage, and accountability with IDS/Pharmacy.
Assists in the development, improvement and review of Standard Operating Procedures and processes.
Provides educational and technical assistance to research staff including orientation and mentoring of new research staff.
Collaborates and participates with teams across the LCI enterprise in a professional and courteous manner.
Interacts professionally with patients and families.
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 Must hold a valid applicable state or South Carolina (as applicable) Board of Nursing license. Bachelor’s Degree (BS) and 1 year of clinical research experience with a pharmaceutical company or Contract Research Organization (CRO) or equivalent experience required; or Master’s Degree (MS) and 0-1 year of clinical research experience with a pharmaceutical company or Contract Research Organization (CRO) or equivalent experience required; or a minimum of 3 years clinical research experience with a pharmaceutical company or Contract Research Organization (CRO) or equivalent experience required with no degree. Bachelor’s Degree in Nursing (BSN) or Master’s Degree in Nursing (MSN) or other health/science degree concentration preferred. CPR certification required. Previous experience in a healthcare setting preferred, especially cancer care and/or clinical research. Certification in clinical research (SoCRA, ACRP, RAPS, etc.) preferred.
Our Commitment to You Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more – so you can live fully at and away from work, including:
Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training
Premium pay such as shift, on call, and more based on a teammate's job
Incentive pay for select positions
Opportunity for annual increases based on performance
Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program
About Advocate Health Advocate Health is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Advocate Health provides care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin. It employs teammates across hospitals and care locations and participates in hundreds of clinical trials and research studies.
Coordinates the clinical, regulatory, business, and other research-related activities and documentation for clinical trials conducted by the Levine Cancer Institute, following industry standards and applicable regulations including FDA/OHRP guidances, GCP and ICH.
Seniority level
Entry level
Employment type
Full-time
Job function
Health Care Provider
Industries: Hospitals and Health Care
#J-18808-Ljbffr