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Position Summary:
We have an exciting opportunity to join our team as a Research Coordinator.
In this role, the successful candidate is responsible for providing moderate to advanced range of coordination of Research studies conducted at the Medical Center assists with the recruitment enrollment grant submissions research data collection and study coordination activities Performs intra operative monitoring and serves as liaison with internal and external funding agencies Ensures the accurate execution of research protocols in accordance with Good Clinical Practices HIPAA and required obligations to patient/subject Principal Investigator Research Team and sponsor Interfaces directly with patients/subjects and Principal Investigator in support of the clinical trials if applicable Establishes liaisons with relevant parties at the Medical Center that may include: Research Nurses Research Pharmacists Program Managers Medical Technicians Clinical Information Systems and regulatory Services Might assist in the initiation and management of research studies Works under general direction or the Project Manager and Principal Investigator
Job Responsibilities:
Human Subjects: Research As applicable oversee the submission of necessary documents required by the NYU Institutional Board IRB NYU Office of Clinical Trials and any other appropriate parties in order to obtain approval to conduct human subjects research e g ensures the update and submission of necessary documents and/or forms to appropriate destination Might prepare audit and submit monthly enrollment statistics to the Office of Clinical Trials and provides other information in timely manner as necessary
Study Regulations: Aware of study regulatory status and keep an up to date copy of regulatory documents
Assists with the informed consent process and ensure that the patient/subject fully understands what is required of them throughout the study Follows through regularly with the patient/subjects reminding them of visits and compliance
May monitor any outward effects or issues regarding patient/subject safety and report this to the Principal Investigator and Project Manager
Data Management - Responsible for collecting and auditing patient information for the research project s This may include abstraction of data from the patient chart e g laboratory or diagnostic test results surgical/radiation treatments delivered adverse drug reactions etc ; abstraction of data for publications or data collection from partnering organizations such as LiveOnY Audits and manages data from and into the database Prepares forms and reports compiles and analyses data statistics and other materials for reports
Conducts study visits qualitative interviews and obtains and documents information within the time frame specified
Budget - Develops a preliminary draft budget and submit to the Director/Principal Investigator Reviews sponsor proposed budget for adequate coverage and recommend changes as appropriate
Assists in the preparation of funding reports to funding agencies and helps identify new potential sponsors/agents for trials and researches
Decision Making and Problems Solving -Combines and evaluates information and data to make decisions about relative importance of information and choosing the best solution to solve problems Resolves complex situations and refers non solved issues and questions with recommendation to supervisor
Participates in special projects and performs other duties as required
Recruitment - Screens potential patients/subjects for eligibility to the study This may include gathering information from the medical record physician referral advertisement and directly scheduling a visit to evaluate the patient/subject Reviews all the elements of the screening process with the Principal Investigator that being: inclusion/exclusion criteria completed informed consent documentation of the event and the patient/subject willingness to participate in the study
Continuous Learning - Position requires ongoing continuing education in all areas of research development training programs are provided through the SOM Promotes own professional growth and development in research role and maintains current expertise in area of practice
Serves as a resource to peers and works collaboratively with other disciplines within the area of expertise
Reporting and Analysis -Researches compiles and consolidates data and conducts preliminary analyzes to data collected for presentation to sponsoring and regulatory agencies Provides reports to all necessary parties e g the principal investigator sponsoring agency etc on the progress of the study as needed Formulates prepares database and generates preliminary measurement reports for review by PI May complete assessments on study subjects/patients following protocol with proper training ; continues to follow through with items and patients as part of the research study
Minimum Qualifications:
To qualify you must have a Bachelor's degree or equivalent in business administration health care administration or related field Minimum of two years of progressively responsible project coordination experience preferably in a research setting Proficiency in using various Microsoft Office applications such as Word Excel Access Power Point and Outlook Familiar with Internet applications Effective oral written communication interpersonal skills Ability to interface effectively with all levels of management and must work and communicate effectively with both internal and external customers Ability to work within a team environment as well as independently Commitment to continuous learning as required by department administration Ability to operate research related equipment Ability to work and make decisions independently Time management skills and ability to multitask Ability to identify analyze and solve problems: Ability to work well under pressure
Preferred Qualifications:
Masters degree in clinical research or public health and/or equivalent experience in clinical trial management and human subjects research
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 $62,400 - $67,000.00 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
Required Skills
Required Experience