Research Study Coordinator

UNC-Chapel HillChapel Hill, NC
4d

About The Position

The primary purpose for this position is to work directly with investigators and other research personnel to initiate and execute imaging research studies at the BRIC . This position will be the primary contact for oncology-related research endeavors at the BRIC , and will work directly with physicians, investigators, and regulatory bodies for study start up, and then directly with physicians and patients in a clinical setting for recruitment and data collection. In addition, this position will work directly with mothers, newborn babies, families, and a variety of clinical populations to collect research data for various studies at the BRIC . Major responsibilities include: recruitment and coordination of study subjects, attendance of tumor board meetings, and communication across study teams to implement study protocols, management of study information, and data collection/entry. The employee must have knowledge and experience in the use of data, preferable medical information. Work environment will include the Magnetic Resonance Imaging ( MRI ) and Positron Emission Tomography ( PET ) scanner room. Employee will undergo safety screening and will need to complete required safety training (including radiation worker training) to work in this environment. This position’s work requires excellent customer service, decision-making and time management skills. Employee will need excellent judgement, concentration and focus to detail. Excellent written and verbal communication skills are required.

Requirements

  • Knowledge and experience in the use of data, preferable medical information
  • Excellent customer service skills
  • Decision-making skills
  • Time management skills
  • Excellent judgement
  • Concentration and focus to detail
  • Excellent written and verbal communication skills

Nice To Haves

  • Self-directed and able to work with minimal supervision
  • Being bilingual in Spanish
  • Experience in administering oncology-related protocols
  • Experience with working with oncology patients and clinical teams
  • Previous experience with OnCore, EPIC , CRMS , and IRB

Responsibilities

  • Recruitment and coordination of study subjects
  • Attendance of tumor board meetings
  • Communication across study teams to implement study protocols
  • Management of study information
  • Data collection/entry

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Education Level

No Education Listed

Number of Employees

11-50 employees

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