Clinical research Coordinator
About The Position
Why Join Our Team? At New York Cancer & Blood Specialists (NYCBS) , we are dedicated to making a difference in the lives of our patients, their families, and our communities. Our passionate team of expert oncologists, hematologists, and healthcare professionals work together to provide world-class cancer care close to home. By offering cutting-edge treatments, innovative research, and a patient-centered approach, we are redefining what’s possible in the fight against cancer and blood disorders. If you want to be part of a growing organization committed to healing, hope, and advanced care , join us and help make a meaningful impact! Job Description: Clinical Research Coordinator Location: Float (Central Park, Brooklyn, Bronx) Hours/Days: 5/8.5 hour days, Mon-Fri 7a-6p Organization: New York Cancer & Blood Specialists (NYCBS) Why Join Our Team? At New York Cancer & Blood Specialists (NYCBS) , we are dedicated to making a difference in the lives of our patients, their families, and our communities. Our passionate team of expert oncologists, hematologists, and healthcare professionals work together to provide world-class cancer care close to home. By offering cutting-edge treatments, innovative research, and a patient-centered approach, we are redefining what’s possible in the fight against cancer and blood disorders. If you want to be part of a growing organization committed to healing, hope, and advanced care , join us and help make a meaningful impact!
Requirements
- STEM Background required
- Associates Degree required (Bachelors preferred)
- Excellent verbal and written communication skills
- Strong interpersonal skills with patients, staff, and healthcare professionals
- Experience with EMR’s
- Attention to detail and professional conduct
- Reliable transportation to travel between NYCBS locations
- Ability to thrive in a fast-paced, collaborative environment
Responsibilities
- Enroll participants into a Clinical Interventional or Observational Study
- Obtain Informed Consent: Explain study procedures, risks, and benefits to participants, ensuring full understanding.
- Coordinate Appointments: Organize and schedule research participant appointments efficiently.
- Manage Research Care: Coordinate care during all research-related appointments, collaborating with other NYCBS departments. Assist at appointments and oversee relevant orders and activities.
- Collect Data: Gather complete and accurate participant data, including medical history, medication review, physical exams, lab tests, ECG, AE review and other required study assessments. Data collected will be entered into EMR, Verily, Onco Trials or Paradigm, and patient update spreadsheets by the CRC- Interventional.
- Track SAEs & Deviations: Document Serious Adverse Events (SAEs) and deviations, reporting them to the sponsor within 24 hours when applicable.
- Provide Regulatory Team with Summaries: Share event summaries with the Regulatory team for timely reporting to regulatory authorities.
- Attend Key Meetings: Participate in Site Initiation Visits (SIVs), research meetings, and sponsor-specified sessions.
Benefits
- Health, Dental, and Vision Insurance (effective on day 1)
- Life Insurance, Short- and Long-Term Disability
- 401k plan with company contributions
- Paid Time Off (PTO) and 8 paid holidays (2 floating)
- Opportunities for professional development and growth within a supportive team
- A culture of collaboration and innovation in a field that’s making a difference
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
