Research Assistant I

Hospital for Special SurgeryNew York, NY
1d$23 - $36

About The Position

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. Assist in the synchronization of research activities under the direction of the Director and serves as a liaison between the clinicians, research staff, and other research assistants. Provide overall administrative & study specific support for research activities including but not limited to: providing timely reports to Director, Institutional Review Board, Principal Investigator, National Institutes of Health and/or sponsor for each research project as well as participating stakeholders. This position will contribute to Arthroplasty research through: -Literature reviews -Data collection & entry -The development and build of Clinical Research Forms -Recruitment process (conducts informed consent process for low risk prospective studies) -Assures that research is done in an accurate, efficient manner while following all GCP guidelines. Ensures that all research related regulatory, institutional, and departmental compliance requirements are met as appropriate. Facilitates completion of all internal documentation needed for research (IRB applications, conflict of interest forms, data collection forms, etc.) Assists in patient care coordination by assuring the completion of research specific protocols integrate well with the patient’s clinical episode of care if the protocol requires Maintains and enhances professional growth through participation in seminars, research meetings, ARJR grand rounds, and internal training sessions to keep abreast of trends in the field of Arthroplasty research.

Requirements

  • Scientific background required.
  • Outstanding record of academic achievement and research experience.
  • 0-2 YEARS OF EXPERIENCE
  • EDUCATION REQUIRED Bachelors

Nice To Haves

  • Proven record of leadership through extracurricular activities or work.
  • Ability to work collaboratively and effectively on a team with people at all levels of an organization.
  • Excellent organization skills (ability to manage several concurrent tasks).
  • Superior oral and written communications skills.
  • Prior research experience
  • Prior Epic experience
  • Prior hospital experience
  • Knowledge of Good Clinical Practice and Good Technology Practice
  • Excellent communication skills
  • Proficient use of computers and software (specifically Microsoft based tools
  • Knowledge of Orthopaedic and/or Rheumatologic terminology is a plus.

Responsibilities

  • Assist in the synchronization of research activities under the direction of the Director and serves as a liaison between the clinicians, research staff, and other research assistants.
  • Provide overall administrative & study specific support for research activities including but not limited to: providing timely reports to Director, Institutional Review Board, Principal Investigator, National Institutes of Health and/or sponsor for each research project as well as participating stakeholders.
  • Contribute to Arthroplasty research through: -Literature reviews -Data collection & entry -The development and build of Clinical Research Forms -Recruitment process (conducts informed consent process for low risk prospective studies)
  • Assures that research is done in an accurate, efficient manner while following all GCP guidelines.
  • Ensures that all research related regulatory, institutional, and departmental compliance requirements are met as appropriate.
  • Facilitates completion of all internal documentation needed for research (IRB applications, conflict of interest forms, data collection forms, etc.)
  • Assists in patient care coordination by assuring the completion of research specific protocols integrate well with the patient’s clinical episode of care if the protocol requires
  • Maintains and enhances professional growth through participation in seminars, research meetings, ARJR grand rounds, and internal training sessions to keep abreast of trends in the field of Arthroplasty research.
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