Atrium Health
Oncology Research Consultant RN - EPIC Treatment Plan Intake Form Builder Atrium
Atrium Health, Charlotte, North Carolina, United States, 28245
Department
80096 Carolinas Medical Center - LC: Clinical Trials: Morehead
Status
Full time
Benefits Eligible
Yes
Hours
40 hours per week
Schedule Details / Additional Information
This role will support the EPIC intake, drug build and treatment validation process, which are essential tasks for clinical trial activation. In addition, this role will collaborate with key stakeholders to ensure EPIC treatment builds are accurately built to comply with protocol requirements and institutional billing standards.
Other Skills
Able to manage multiple tasks producing high quality work
Able to work across multiple teams within the CTO and other LCI departments. Self-starter and results driven
Strong attention to details
Strong organizational skills
Remote / hybrid position, M - F (8am-5pm)
Eligible States
AL, CO, FL, GA, ID, KS, KY, ME, MI, NC, SC, VA, VT, WA
Pay Range
$43.30 - $64.95
Essential Functions
Competently fulfills the job responsibilities of the Oncology Research Coordinator, and:
Assists Principal Investigator and team in evaluating feasibility of research studies.
Develops study budget in collaboration with team.
Coordinates documentation for regulatory requirements.
Coordinates trial-related activity of patients on protocols.
Coordinates, follows, and evaluates patient participation in clinical trials to ensure compliance with the protocol.
Coordinates protocol-specific clinical tasks including patient assessment, eligibility screening, symptom management, toxicity assessment, and monitoring of responses.
Coordinates protocol-specific scheduling of tests and specimen collection across LCI locations.
Monitors and reports significant study events including adverse events and protocol amendments, activity, status, and closures.
Performs required study procedures, collects data, analyzes data and makes decisions regarding the clinical research study conduct, including initial screening, assessment, care, reassessment and modification of care in consultation with PI and team.
Assists in data analysis and drafting of clinical study reports.
Develops, updates and/or implements standard operating procedures (SOPs).
Serves as a team leader.
Serves as the key resource for Principal Investigator, physicians and research team and acts as the primary liaison with sponsors to facilitate study initiation, execution and termination.
Ensures accurate and timely data collection, submission, and query resolution.
Coordinates protocol-level documentation to ensure regulatory and institutional compliance.
Educates patients and families about research studies, treatments, side effects and follow-up, as appropriate.
Coordinates protocol activities across Levine Cancer Institute.
Collaborates with investigators through attendance at Section meetings, conferences, and other meetings.
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 and 3 years of clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required; or Master's Degree and 2 years of clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required; or a minimum of 6 years clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required with no degree. Bachelor's Degree in Nursing or Master's Degree in Nursing 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. Supervisory experience preferred.
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.
Compensation
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
Benefits and more
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. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies.
Core Responsibilities and Activities Conducts and develops all aspects of clinical, regulatory, business, and other research-related activities and documentation for clinical trials on behalf of the Levine Cancer Institute, following industry standards and applicable regulations including FDA/OHRP guidance, GCP and ICH.
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80096 Carolinas Medical Center - LC: Clinical Trials: Morehead
Status
Full time
Benefits Eligible
Yes
Hours
40 hours per week
Schedule Details / Additional Information
This role will support the EPIC intake, drug build and treatment validation process, which are essential tasks for clinical trial activation. In addition, this role will collaborate with key stakeholders to ensure EPIC treatment builds are accurately built to comply with protocol requirements and institutional billing standards.
Other Skills
Able to manage multiple tasks producing high quality work
Able to work across multiple teams within the CTO and other LCI departments. Self-starter and results driven
Strong attention to details
Strong organizational skills
Remote / hybrid position, M - F (8am-5pm)
Eligible States
AL, CO, FL, GA, ID, KS, KY, ME, MI, NC, SC, VA, VT, WA
Pay Range
$43.30 - $64.95
Essential Functions
Competently fulfills the job responsibilities of the Oncology Research Coordinator, and:
Assists Principal Investigator and team in evaluating feasibility of research studies.
Develops study budget in collaboration with team.
Coordinates documentation for regulatory requirements.
Coordinates trial-related activity of patients on protocols.
Coordinates, follows, and evaluates patient participation in clinical trials to ensure compliance with the protocol.
Coordinates protocol-specific clinical tasks including patient assessment, eligibility screening, symptom management, toxicity assessment, and monitoring of responses.
Coordinates protocol-specific scheduling of tests and specimen collection across LCI locations.
Monitors and reports significant study events including adverse events and protocol amendments, activity, status, and closures.
Performs required study procedures, collects data, analyzes data and makes decisions regarding the clinical research study conduct, including initial screening, assessment, care, reassessment and modification of care in consultation with PI and team.
Assists in data analysis and drafting of clinical study reports.
Develops, updates and/or implements standard operating procedures (SOPs).
Serves as a team leader.
Serves as the key resource for Principal Investigator, physicians and research team and acts as the primary liaison with sponsors to facilitate study initiation, execution and termination.
Ensures accurate and timely data collection, submission, and query resolution.
Coordinates protocol-level documentation to ensure regulatory and institutional compliance.
Educates patients and families about research studies, treatments, side effects and follow-up, as appropriate.
Coordinates protocol activities across Levine Cancer Institute.
Collaborates with investigators through attendance at Section meetings, conferences, and other meetings.
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 and 3 years of clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required; or Master's Degree and 2 years of clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required; or a minimum of 6 years clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required with no degree. Bachelor's Degree in Nursing or Master's Degree in Nursing 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. Supervisory experience preferred.
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.
Compensation
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
Benefits and more
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. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies.
Core Responsibilities and Activities Conducts and develops all aspects of clinical, regulatory, business, and other research-related activities and documentation for clinical trials on behalf of the Levine Cancer Institute, following industry standards and applicable regulations including FDA/OHRP guidance, GCP and ICH.
#J-18808-Ljbffr