Manager, Research - New York, United States - Hospital for Special Surgery

Hospital for Special Surgery

Verified Company

New York, United States

1 week ago

Posted by:

Mark Lane

beBee recruiter

Description

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...

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

Neuromuscular, Research Manager

Full-Time

Responsibilities:

Serves as primary contact for CDA and CTA, acting as a liaison between PI, CRO and sponsor:
Primary site contact for the negotiation of CDA, CTA and budget; responsible for tracking, processing and implementing clinical research budgets with sponsors for new studies and amendments.
Primary contact for clinical trial budget creation; oversees finances related to the clinical trials including budget, invoicing, salary sourcing, and financial reconciliations.
Directly manages daytoday activities of multiple research coordinators, project assistants and volunteers in the department of Neurology.
Assists in recruiting, hiring, mentoring and implementing onboarding and trainings for new research staff. Completes developmental plans and performance management.
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. This includes the supervision of multidisciplinary teams involved in the successful conduct of the study as well as research assistants I and II and clinical research coordinators assigned to independent research studies.
Spearheads efforts to meet patient enrollment targets related to independent research studies. To that end, develops and implements various recruitment strategies.
Responsible for completing, tracking and monitoring IRB submissions for initial approvals, reapprovals, amendments and closeouts of all studies
Manages and executes IRB submissions for initial approvals, reapprovals, amendments, etcEnsures timeliness and accuracy of submissions and no lapses in approvals for the study. Directs research coordinators in this effort as well.
Compiles and assists in analyzing and interpreting data in preparation for a presentation, sponsor/regulatory agency, publication, etcwith the assistance of project investigator
Performs advanced data queries 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 design and development of new protocols, prospective databases, SOPs training protocols and new initiatives taken on by the department. This may include design of database and case report forms for investigator initated trials as well tools to facilitate data collection as requested for specific projects (calendars, schedules, tracking logs)
Represents the Principal Investigator in departmental audits as well as external audits performed by representatives of the sponsor for each clinical research project. Works closely with HSS internal monitor for guidance on these activities.
Conducts study specific team meetings(weekly) to ensure timely progress of patient enrollment and study activities.
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 may be required.
Manages all space, equipment and supply needs of the neurology research and neuromuscular clinic programs
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.
Assists /work with the development and implementation of independent research projects (completing all IRB submissions/followup) for nonresearch team (clinic team) members' studies
Develops and implements ongoing quality improvement activities for research team. Ensures safe, efficient and quality research oversight, constantly updating practices based on industry standards