Sr Clinical Research Coord

Job Summary

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.

• 2+ years:
  Completion of a bachelor’s or associate degree from an accredited nursing program (RN) plus a minimum of three (3) years oncology research experience OR Completion of a bachelor’s degree in a related field plus a minimum of three (3) years oncology research experience.
• Must be a Certified Clinical Research Coordinator (CCRC-ACRP) or Certified Clinical Research Professional (CCRP-SoCRA).
• Previous coordinator experience.
• Oncology research 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.