Sr Clinical Research Coordinator

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Community Health Network was created by our neighbors for our neighbors. Over 60 years later community is still the heart of our organization. It means providing our neighbors with the best care possible backed by state-of-the-art technology. It means getting involved in the communities we serve through volunteer opportunities and benefits initiatives. It means ensuring our dedicated caregivers can learn and grow to stay at the top of their fields and to better serve our patients. And above all it means exceptional care simply delivered and we couldnt do it without you.

Make a Difference
The Sr. Clinical Research Coordinator is responsible for independently running and operating multiple research protocols in conjunction with the Principal Investigator and serves as a lead in the clinical research unit.
Determines facility and supply needs required for set-up and implementation of research protocols.
Assists in identifying study related procedures for the project budget.
Prepares for and is present for sponsor representative site visits.
Provides regional leadership for assigned research.
Be able to perform all of the duties of the Clinical Research Coordinator.
Trains and/or may supervise Clinical Research Assistants and/or Clinical Research Coordinators.
Assists with preparing for and conducting qualification study initiation interim monitoring and close-out visits at investigator sites in conjunction with the Clinical Research Manager.

Your exceptional skills and qualifications
2 year / Associate Degree required
3 years: Clinical research or an equivalent combination of relevant education and/or experience (required)
Must be a Certified Clinical Research Coordinator (CCRC-ACRP) or Certified Clinical Research
Professional (CCRP-SoCRA) (within 3 years of hire)
Previous coordinator experience
Ability to be detail oriented
Ability to be organized
Ability to communicate effectively both orally and in writing with all levels of the organization
Ability to effectively use interpersonal skills
Ability to independently manage time and priorities
Ability to navigate EMRs
Ability to travel between locations
Ability to use patient care skills to provide an exceptional experience
Ability to utilize Microsoft Office Suite
Demonstrates compliance with hospital standards policies and procedures
Ability to communicate effectively both orally and in writing

Shelbourne Knee Center Specific Information:

As the senior research coordinator for the Shelbourne Knee Center tasks will include the following:

• Oversee and manage IRB submissions amendments and yearly continuing reviews for the network within the IRIS platform.
• Ensure IRB compliance for key study personnel on each study.
• Serve as contact and point person for network led initiatives as it pertains to Shelbourne Knee Center research
• Key contributor to the development of new studies including the study design data collection process and statistical analysis plan
• Assist the research and clinical teams with the opportunity to lead in clinical research tasks such as: Authoring research documents including manuscripts for publications abstracts for national orthopedic conferences and presentations to be delivered at conferences
• Completing literature reviews on orthopedic topics to be used for future or ongoing studies
• Developing sponsored studies or grant proposals including determining financial feasibility and project budgeting
• Coordinating of sponsor visits and external audits for funded studies
• Assist research coordinators with the consenting of patients