Recruitment Consultant - Temporary

This is a temporary position to support clinical research trials.
**A bonus will be paid on successful qualification of patients onto clinical trial studies**

Duties/Responsibilities:
Manage the recruitment of subjects for study participation via methods including, but not limited to: database review, contacting prior patients, reaching out to patients identified by outreach or advertising, patients who have recently completed a previous study
Develop and conduct pre-screen procedures utilizing sponsor/trial specific pre-screen questionnaire to evaluate potential eligibility for a clinical trial
Responsible for developing a rapport with and providing excellent customer service to prospective patients
Answer questions regarding participation in a clinical research trial including but not limited to fundamental of informed consent as well as general information regarding study procedures
Enter and track subjects into the site’s clinical database ensuring accurate contact information and basic patient demographics
Schedule subjects for on-site screening visits and collaborate with Site Director regarding staffing needs
Evaluate necessary information from the research participants (i.e., HIPAA, Medical Chart Release Authorization, Questionnaires) and when applicable, medical records
Understand the protocol (i.e., study timelines, inclusion and exclusion criteria, study requirements)
Maintain, track, and perform quality checks on various site logs (i.e., study subject enrollment logs, pre-screen, and screening logs) as needed
Attend community events to promote VelocityClinical Research and advertise for studies
Track and assist in evaluating responses for individual patient outreach initiatives including but not limited to centralize advertising campaigns and local site-initiated campaigns to assist Site Director in determining success and ROI of campaign
Maintain confidentiality of patient protected health information
Other duties as assigned

Required Skills/Abilities:
Demonstrated knowledgeof medical terminology
Proficient in the use of the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
Ability to work in a fast-paced environment
Strong verbal, written, and organizational skills
Strong interpersonal and communication skills
Ability to work as a team player
Demonstrated abilityto read, write, and speak English
Ability to multi-task
Ability to followwritten guidelines
Ability to work independently, plan and prioritize with minimal guidance
Ability to be flexible/adapt as daily schedule may change rapidly
Must be detail oriented
Proficient problem solving and strategicdecision making ability.
Proficient in accepting individual responsibility for actions taken and demonstrating professionalism when judged, critiqued and/or praised.
Demonstrated leadership ability
Be analytical with a strong focus on reporting and results to make informed data-driven recommendations and decisions

A bonus will be paid on successful qualification of patients onto clinical trial studies