Clinical Research Coordinator II - Tisch Cancer Center

Mount Sinai; New York (NY); On-site; USD 66,199 - 90,000; Full time

Job summary

Mount Sinai Medical Center in New York is seeking a Clinical Research Coordinator II to oversee clinical research activities within the Tisch Cancer Center. You will coordinate ongoing trials, manage patient data, and ensure compliance with all regulatory requirements.

The ideal candidate has a Bachelor’s degree in sciences and 2 years of clinical research experience, with a preference for those with oncology knowledge. The role offers an annual salary of $66,199.99 - $90,000.04.

Qualifications

• 2 years of clinical research experience.
• Experience in oncology is preferred.

Responsibilities

• Coordinate activities of ongoing clinical trials.
• Obtain informed consent under supervision.
• Manage study data of ongoing clinical trials.
• Ensure compliance with regulatory requirements.

Skills

Clinical research skills

Data management

Informed consent procedures

Oncology knowledge

Education

Bachelor's degree in sciences or related field

Job description

Description

A Clinical Research Coordinator (CRC) II position is currently available within the Tisch Cancer Center. 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, obtain informed consent, collect, maintain and organize study information, and assist 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.

The Tisch Cancer Center 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, which is 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 the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
• Obtain informed consent under supervision of the study investigator(s); educate participants regarding study requirements.
• Screen patients for eligibility and register subjects with sponsoring agency.
• Coordinate research team to ensure compliance with 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 investigator(s) and sponsoring agency.
• Coordinate activities pertinent to the safeguarding of patients’ rights in research.

Manage study data of ongoing clinical trials under supervision of the Principle 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 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 proper 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

Performs other job related duties as required, which may include but not limited to:

• Participate in Investigators’ Meeting and assist with coordinating Study Initiation Visits.
• Attend divisional/departmental/institutional educational and training seminars.
• Contact local physicians to obtain source documentation and subject survival status.
• Educate new staff regarding overview of clinical research, office policy and procedures, data submission, patient registration and specimen handling.

Qualifications

• Bachelor's degree in sciences or related field
• 2 years of clinical research
• Oncology experience preferred

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. We are deeply committed to fostering an environment where all faculty, staff, trainees, patients, visitors, and the communities we serve feel respected and supported. Our goal is to create a healthcare and learning institution that actively works to remove barriers, address challenges, and promote fairness in all aspects of our organization.

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 $66,199.99 - $90,000.04 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/incentive, differential pay or other forms of compensation or benefits.