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Position Summary:

We have an exciting opportunity to join our team as a Clinical Research Coordinator - Center for Bio-specimen Research and Development.

The Center for Bio specimen Research and Development is a centralized infrastructure launched to provide support to the clinical research community with the acquisition processing storage and distribution of biospecimens tissue biofluids for clinical trials and biomedical research projects The Biorepository works closely under the general direction of the Center Director with Lab Management Sample Management Inventory and documenting clinical data in the LIMS database Position Summary: The Research Coordinator works closely with the Principal Investigator to coordinate the collection processing and distribution of human tissue and biofluids for the biorepository; ensures accurate data entry and management quality assurance and organization

Job Responsibilities:

• Additional responsibilities as needed including: Help in the development of SOPs policy changes education sessions and quality improvement projects
• Work with licensed clinicians to develop tracking forms for all active trials maintain tracking forms throughout the life cycle of the protocol
• Provide updates to study team members regarding changes to workflow or patient related specific needs according to protocol modifications
• Schedule participants according to the approved protocol; coordinate with ancillary service providers to ensure patients remain adherent to the protocol
• Prepare for study visits: bio specimen collection research ticket preparation lab and EKG orders scheduling of biopsies and scans facilitating RECIST form AE and Conmed form completion in conjunction with licensed professional and other tasks as needed
• Act as primary point of contact for all bio specimen collections
• Compile and submit weekly pharmacy lists to investigational pharmacy
• Monitor infusion chair assignments; assure patient assignments are aligned with protocol requirements; make necessary requests for changes on as needed basis
• Help to reconcile any clinical discrepancies in data with RDAs and RCs
• Maintain follow up calendar ensuring all survival follow up assessments are completed per the protocol; performs assessments not requiring licensure
• May perform EKGs with documented training
• Initiates vial assignment by DCU and coordinates with Infusion Nurses and Pharmacy to ensure timely dispensation of IP
• Participates in Pre Screening activities to identify patients that may be eligible for a clinical trial
• Under the supervision of licensed clinicians administers ancillary assessments i e Quality of Life Exam
• Participates in the feasibility and complexity assessment process for new protocols
• Assists patients in understanding the schedule of assessments according to the approved protocol coordination of appointments and ancillary services under the supervision of a licensed clinician but clinician does not have to be physically present
• Under the supervision of investigator may take part in AE and Con Med documentation and reporting activities such as SAE and ECI reports All documentation must be verified and signed by licensed clinicians before submission and all assessments must be made by a licensed clinician
• Write research notes in EPIC may not make assessments
• Helps compile enrollment packet materials must be reviewed and signed by investigator

Minimum Qualifications:

To qualify you must have a Bachelor s Degree or equivalent combination of education and experience required Computer literate with good interpersonal writing and verbal communication skills 2 years relevant experience required Effective oral written communication interpersonal skills Must be able to work under the direction of supervision Ability to identify analyze and solve problems Time management skills and ability to work well under pressure Proficiency in using various Microsoft Office applications such as World Excel Access Power Point and Outlook Familiar with Internet applications

Qualified candidates must be able to effectively communicate with all levels of the organization.NYU Grossman School of Medicine provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you'll feel good about devoting your time and your talents.NYU Grossman School of Medicine is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sex, sexual orientation, transgender status, gender dysphoria, national origin, age, religion, disability, military and veteran status, marital or parental status, citizenship status, genetic information or any other factor which cannot lawfully be used as a basis for an employment decision. We require applications to be completed online.
If you wish to view NYU Grossman School of Medicine's EEO policies, please click here. Please click here to view the Federal "EEO is the law" poster or visit https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm for more information.

NYU Langone Health provides a salary range to comply with the New York state Law on Salary Transparency in Job Advertisements. The salary range for the role is $67,771.14 - $72,758.40 Annually. Actual salaries depend on a variety of factors, including experience, specialty, education, and hospital need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.

To view the Pay Transparency Notice, please click here