Clinical Research Coordinator (Varying levels); Benign Gynecology

UVA Health

12h•Onsite

About The Position

The Department of OBGYN is seeking a non-licensed OR licensed Clinical Research Coordinator (Varying levels) to join our Benign Gynecology team. Clinical Research Coordinators perform a range of clinical research duties including working with research participants, processing laboratory specimens, data entry, record keeping, materials preparation, and reviewing of prospective research participants. Clinical Research Coordinators will also assist with clinical trial-related activities, recruit, screen, and consent potential study participants, schedule study visits, prepare and maintain study documentation, collect data at all study visits, compile adverse event data, and manage all data collected. Individuals seeking this position must have strong organization skills, have the ability to problem-solve, work well in a team environment, have excellent written and oral communication skills, strong assessment skills, and demonstrate an ability to learn new information quickly.

Requirements

Strong organization skills
Ability to problem-solve
Work well in a team environment
Excellent written and oral communication skills
Strong assessment skills
Ability to learn new information quickly
For CRC 1 non-licensed: Bachelor's Degree Required or equivalent combination of experience, education and or certifications.
For CRC 2 non-licensed: Bachelor's Degree Required or equivalent combination of experience, education and or certifications; At least one year of clinical research experience.
For CRC 3 non-licensed: Bachelor's Degree Required or equivalent combination of experience, education and or certifications; Minimum of 3 years of clinical research experience required; Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is required within one year.
For CRC 4 non-licensed: Bachelor's Degree Required or equivalent combination of experience, education and or certifications; At least seven years of clinical research experience demonstrating progressive levels of responsibility and complexity of work; Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is required within one year of hire.
For Licensed Professionals: MUST be licensed to Practice in Clinical Profession such as Registered Nurse, Athletic Training, Pharmacology, Medical Technology, Physical Therapy, Registered Respiratory Therapy.
For CRC 1 licensed: Bachelor's Degree Required or equivalent combination of experience, education and or certifications (Nursing Diploma may substitute for Degree for Licensed Registered Nurse).
For CRC 2 licensed: Bachelor's Degree Required or equivalent combination of experience, education and or certifications (Nursing Diploma may substitute for Degree for Licensed Registered Nurse); At least one year of clinical research experience.
For CRC 3 licensed: Bachelor's Degree Required or equivalent combination of experience, education and or certifications (Nursing Diploma may substitute for Degree for Licensed Registered Nurse); A minimum of 3 years of clinical research experience required; Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is required within one year of hire.
For CRC 4 licensed: Bachelor's Degree Required or equivalent combination of experience, education and or certifications (Nursing Diploma may substitute for Degree for Licensed Registered Nurse); At least seven years of clinical research experience demonstrating progressive levels of responsibility and complexity of work; Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is required within one year of hire.
Background checks, pre-employment health screenings, and drug screenings will be conducted on all new hires prior to employment.
Will not consider candidates who require immigration sponsorship now or in the future.

Nice To Haves

Some experience in a healthcare setting and/or knowledge of medical terminology (preferred for CRC 1 & 2 non-licensed)
Master’s degree may substitute for 1 year of clinical research experience (for CRC 3 non-licensed)
Master’s or other advanced degree may substitute for one year of clinical research experience (for CRC 4 non-licensed and CRC 4 licensed)
Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is preferred at the time of hire (for CRC 3 non-licensed)

Responsibilities

Recruit, screen, and enroll study participants who meet research criteria for multiple clinical trials in the Division of GynOnc.
Obtain informed consent from study participants and maintain telephone and in-person contact.
Work closely with Principal Investigators and other study team members on all clinical research projects assigned.
Notify PI and/or supervisor of any potential issues with the study or subject status.
Collect subject data, enter and analyze data, and compile reports, adhering to proper research protocols.
Communicate effectively with study Sponsor(s).
Prepare documentation, reports, graphs, and other materials.
Keep appropriate logs, track participants, and prepare study materials.
Process, prepare, and ship laboratory specimens.
Other duties may be assigned.