Clinical Research Coordinator

Location US-NY-New York
Posted Date 1 month ago(9/9/2021 12:09 PM)
Job ID
2021-14574
Category
Research & Academia - All Openings
Emp Status
Regular Full-Time
Hours per Week
35
Shift
Days

Overview

How you move is why we’re here. ®
Now more than ever.

Get back to what you need and love to do.

The possibilities are endless...

 

Now more than ever, our guiding principles are helping us in our search for exceptional talent - candidates who align with our unique workplace culture and who want to maximize

 the abundant opportunities for growth and success.

 

If this describes you then let’s talk!

 

HSS is consistently among the top-ranked hospitals for orthopedics and rheumatology by U.S. News & World Report. As a recipient of the Magnet Award for Nursing Excellence, HSS was the first hospital in New York City to receive the distinguished designation. Whether you are early in your career or an expert in your field, you will find HSS an innovative, supportive and inclusive environment.

Working with colleagues who love what they do and are deeply committed to our Mission, you too can be part of our transformation across the enterprise.

 

Clinical Research Coordinator

Full-Time

 

Clinical Research Coordinator Position in Neurology at the Hospital for Special Surgery in New York, NY

 

SUMMARY:

Responsible for clinical and data management activities associated with clinical research at a service specific level.  Performs data collection, data entry and analysis for studies as appropriate. We prefer applicants be comfortable working with patients and their families. 

DUTIES AND RESPONSIBILITIES:

  • Conducts the informed consent process on studies as appropriate (requires appropriate training and certification of human research subjects training).
  • Under supervision, monitors patients’ progress while on clinical trials via observation, clinical interactions and performance of study-specific assessments as outlined in protocols.
  • Manages data collection specific to research studies including but not limited to the performance of measurements for applicable studies, collection of clinical data from patients directly, and manage the performance of all other duties as put forth in the protocol.
  • Spearheads efforts to meet subject enrollment targets related to independent research studies. To that end, develops and implements various recruitment strategies.
  • Assists with IRB submissions for initial approvals, continuing reviews, amendments, etc… Ensures timeliness and accuracy of submissions and no lapses in approvals for the study.
  • Ensures accuracy of personnel transcribing data from a paper case report form (CRF) into an electronic format.
  • Performs data queries reconciliation when needed. Provides timely reports to Institutional Review Board, Principal Investigator, National Institutes of Health and/or sponsor for each research project.
  • Participates in the development of new protocols, prospective databases and new initiatives taken on by the department. This may include independent design of databases and tools to facilitate data collection as required for specific projects (calendars, schedules, tracking logs).
  • Compiles and assists in analyzing and interpreting data with the assistance of PI for reports to IRB, monitor NIH, NIH and/or sponsor, presentations and publications of various research projects.
  • Collaborates with the research team and research administration, as needed, to ensure that research subjects are treated in accordance with all mandated requirements. Ensures that standards regarding subject registration, protocol specific tests, and required documentation are adhered to.  Reports deviations as appropriate and resolves issues when possible.  Escalates issues to supervisor as needed.
  • Prioritizes and schedules work activities to ensure that workflow is controlled and meets the need of the department. Communicates and maintains institutional/departmental policies, standard operating procedures, quality standards, improvement initiatives and external legal regulations/regulatory requirements.
  • Responsible for the handling, packaging, and shipping of dangerous goods under supervision and in compliance with State and Federal regulations. These specimens may include tissue, blood, dry ice, and chemicals.  Certification in these procedures is required in accordance with the Federal Regulations.  Knowledge of good clinical practice for the handling of specimens and blood required.
  • Maintains and enhances professional growth through participation in seminars, professional affiliations, and internal training sessions to keep abreast of trends in the field of research data management.

 

 

 

Other Requirements

Qualified candidates are effective multi-taskers, proven problem solvers and are detail-oriented. Applicants must have strong organizational skills, be good decision-makers, demonstrate flexibility in his/her approach, maintain a high level of professionalism and have excellent interpersonal and communication skills.

MINIMUM JOB REQUIREMENTS:
Education/Training: Bachelor’s degree
Experience: 1-3 years’ experience in clinical research preferred but not required
Proficient use of Microsoft Office ((Word, Excel, and Adobe Acrobat, Tracked Changes functionality).
Knowledge of medical terminology and familiarity of clinical trials (federal, state and local regulations), clinical data and its analysis preferred but not required.

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