Mount Sinai Health System
Clinical Research Coordinator II - Tisch Cancer Institute
Mount Sinai Health System, New York, New York, us, 10261
Description
A Clinical Research Coordinator (CRC) II position is currently available within the Tisch Cancer Institute. Duties will include activities such as data collection and management of patient clinical information, timely collection of protocol‑related samples including shipment to outside entities as required, obtaining informed consent, collecting, maintaining and organizing study information, and assisting with other day‑to‑day operations as required. Under minimal supervision, the Clinical Research Coordinator II will manage a workload that includes studies of increased complexity.
About the Tisch Cancer Institute The Tisch Cancer Institute is a vital component of the Icahn School of Medicine at Mount Sinai Hospital and plays a key role in the Mount Sinai Health System, one of the largest health care systems in the nation. We are a National Cancer Institute (NCI)–designated center and provide a multidisciplinary approach to cancer treatments and clinical breakthroughs that may one day put an end to cancer.
Responsibilities
Coordinates activities of ongoing clinical trials.
Assists in activities related to clinical research studies, including answering phone calls, screening participants for eligibility, registering subjects with the sponsoring agency, and administering lifestyle questionnaires.
Obtains informed consent under the supervision of the study investigator(s) and educates participants regarding study requirements.
Screen patients for eligibility and register subjects with the sponsoring agency.
Coordinate the research team to ensure compliance with the planned treatment protocol, including required laboratory and radiographic testing.
Secure, deliver, and ship blood and/or tissue samples, radiographs, and other clinical specimens as required by protocol.
Act as liaison between investigators and the sponsoring agency.
Coordinate activities pertinent to safeguarding patients’ rights in research.
Manage study data of ongoing clinical trials under the supervision of the Principal Investigator(s).
Ensure accurate and complete compilation of subject data through chart reviews.
Collect and record study data on Case Report Forms (CRFs) and submit forms in a timely manner according to study guidelines.
Meet with internal and sponsor‑appointed monitors to ensure accuracy of subject data and compliance with the research protocol.
Maintain source documents and subject files in accordance with Mount Sinai School of Medicine (MSSM) Standard Operating Procedures (SOPs).
Assist with analyzing data as needed.
Ensure compliance with institutional and national regulatory requirements.
Report adverse events and serious adverse events in accordance with MSSM Institutional Review Board (IRB) SOPs, sponsor guidelines, and federal regulations.
Assist the PI and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
Perform other job‑related duties as required, which may include but are not limited to:
Participate in investigators’ meetings and assist with coordinating study initiation visits.
Attend divisional, departmental, and institutional educational and training seminars.
Contact local physicians to obtain source documentation and subject survival status.
Educate new staff regarding the overview of clinical research, office policies and procedures, data submission, patient registration, and specimen handling.
Qualifications
Bachelor’s degree in sciences or a related field.
At least 2 years of clinical research experience.
Preferred qualifications:
Working knowledge of Good Clinical Practice guidelines and federal research regulations.
Demonstrated strong organizational and communication skills.
Oncology experience preferred.
Comfortable communicating clinical information to medical personnel.
Strong computer literacy.
Employer Description The Mount Sinai Health System is committed to fostering an environment where everyone can contribute to excellence. We share a common dedication to delivering outstanding patient care, and we are dedicated to building a supportive and welcoming environment where everyone has the opportunity to thrive and advance professionally.
Equal Opportunity Employer The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law.
Compensation The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $63,653.84 to $85,000.06 annually. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses, incentives, differential pay, or other forms of compensation or benefits.
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About the Tisch Cancer Institute The Tisch Cancer Institute is a vital component of the Icahn School of Medicine at Mount Sinai Hospital and plays a key role in the Mount Sinai Health System, one of the largest health care systems in the nation. We are a National Cancer Institute (NCI)–designated center and provide a multidisciplinary approach to cancer treatments and clinical breakthroughs that may one day put an end to cancer.
Responsibilities
Coordinates activities of ongoing clinical trials.
Assists in activities related to clinical research studies, including answering phone calls, screening participants for eligibility, registering subjects with the sponsoring agency, and administering lifestyle questionnaires.
Obtains informed consent under the supervision of the study investigator(s) and educates participants regarding study requirements.
Screen patients for eligibility and register subjects with the sponsoring agency.
Coordinate the research team to ensure compliance with the planned treatment protocol, including required laboratory and radiographic testing.
Secure, deliver, and ship blood and/or tissue samples, radiographs, and other clinical specimens as required by protocol.
Act as liaison between investigators and the sponsoring agency.
Coordinate activities pertinent to safeguarding patients’ rights in research.
Manage study data of ongoing clinical trials under the supervision of the Principal Investigator(s).
Ensure accurate and complete compilation of subject data through chart reviews.
Collect and record study data on Case Report Forms (CRFs) and submit forms in a timely manner according to study guidelines.
Meet with internal and sponsor‑appointed monitors to ensure accuracy of subject data and compliance with the research protocol.
Maintain source documents and subject files in accordance with Mount Sinai School of Medicine (MSSM) Standard Operating Procedures (SOPs).
Assist with analyzing data as needed.
Ensure compliance with institutional and national regulatory requirements.
Report adverse events and serious adverse events in accordance with MSSM Institutional Review Board (IRB) SOPs, sponsor guidelines, and federal regulations.
Assist the PI and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
Perform other job‑related duties as required, which may include but are not limited to:
Participate in investigators’ meetings and assist with coordinating study initiation visits.
Attend divisional, departmental, and institutional educational and training seminars.
Contact local physicians to obtain source documentation and subject survival status.
Educate new staff regarding the overview of clinical research, office policies and procedures, data submission, patient registration, and specimen handling.
Qualifications
Bachelor’s degree in sciences or a related field.
At least 2 years of clinical research experience.
Preferred qualifications:
Working knowledge of Good Clinical Practice guidelines and federal research regulations.
Demonstrated strong organizational and communication skills.
Oncology experience preferred.
Comfortable communicating clinical information to medical personnel.
Strong computer literacy.
Employer Description The Mount Sinai Health System is committed to fostering an environment where everyone can contribute to excellence. We share a common dedication to delivering outstanding patient care, and we are dedicated to building a supportive and welcoming environment where everyone has the opportunity to thrive and advance professionally.
Equal Opportunity Employer The Mount Sinai Health System is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude, or treat individuals differently based on race, color, national origin, age, religion, disability, sex, sexual orientation, gender, veteran status, or any other characteristic protected by law.
Compensation The Mount Sinai Health System (MSHS) provides salary ranges that comply with the New York City Law on Salary Transparency in Job Advertisements. The salary range for the role is $63,653.84 to $85,000.06 annually. Actual salaries depend on a variety of factors, including experience, education, and operational need. The salary range or contractual rate listed does not include bonuses, incentives, differential pay, or other forms of compensation or benefits.
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