Clinical Research Coordinator (Varying levels); Benign Gynecology

Benefits

Qualifications

• •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
• •Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications
• •Licensure: None
• •Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications
• •Experience: At least one year of clinical research experience
• •Licensure: None
• •Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications
• •Experience: Minimum of 3 years of clinical research experience required
• •Master’s degree may substitute for 1 year of clinical research experience
• •Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications
• •Experience: At least seven years of clinical research experience demonstrating progressive levels of responsibility and complexity of work
• •Master’s or other advanced degree may substitute for one year of clinical research experience
• •Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is required within one year of hire
• •Licensure Requirement: MUST be licensed to Practice in Clinical Profession such as (but not limited to):
• •Registered Nurse
• •Athletic Training
• •Pharmacology
• •Medical Technology
• •Physical Therapy
• •Registered Respiratory Therapy
• •CRC 1 licensed*
• •Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications
• •Nursing Diploma may substitute for Degree for Licensed Registered Nurse
• •CRC 2 licensed*
• •Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications
• •Nursing Diploma may substitute for Degree for Licensed Registered Nurse
• •Experience: At least one year of clinical research experience
• •CRC 3 licensed*
• •Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications
• •Nursing Diploma may substitute for Degree for Licensed Registered Nurse
• •Experience: A minimum of 3 years of clinical research experience required
• •Master’s or advanced degree may substitute for 1 year of clinical research experience
• •Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is required within one year of hire
• •CRC 4 licensed*
• •Education: Bachelor's Degree Required or equivalent combination of experience, education and or certifications
• •Nursing Diploma may substitute for Degree for Licensed Registered Nurse
• •Experience: At least seven years of clinical research experience demonstrating progressive levels of responsibility and complexity of work
• •Master’s or other advanced degree may substitute for one year of clinical research experience
• •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
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Responsibilities

• •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
• •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
• •In addition to the above job responsibilities, other duties may be assigned
• •This is primarily a sedentary job involving extensive use of desktop computers
• •The job does occasionally require traveling some distance to attend meetings, and programs
• •11 more items(s)