Phlebotomy required)

AIDS Healthcare Foundation•Fort Lauderdale, FL

5h•Onsite

About The Position

AMAZING INDIVIDUALS WORKING FOR POSITIVE PEOPLE at AIDS Healthcare Foundation! Does the idea of doing something that really makes a difference in people’s lives while being well-compensated intrigue you? Are you looking to work for an organization that encourages growth and success from each and every one of its employees? If so, AIDS Healthcare Foundation is the place for you! Founded in 1987, AIDS Healthcare Foundation is the largest specialized provider of HIV/AIDS medical care in the nation. Our mission is to provide cutting edge medicine and advocacy, regardless of ability to pay. Through our healthcare centers, pharmacies, health plan, research and other activities, AHF provides access to the latest HIV treatments for all who need them. AHF’s core values are: Patient-Centered, Value Employees, Respect for Diversity, Nimble, Fight for What’s Right. A Research Coordinator / Medical Assistant / Phlebotomist contributes to AHF by projecting and integrating our core values. Helping to find ways to improve AHF’s cutting edge approach by following the lead of the Research Department leadership and Lead Research Coordinator. A Research Coordinator I enhances the reputation of AHF by innovative finds through the Research Department that help improve patient care. You will be a passionate advocate for our top initiatives. To be successful as a Research Coordinator I it is crucial to ensure that the AHF Core Values and Mission stay top of mind with all that you do. At AHF we are nimble and able to adapt in a dynamic environment to assist in providing the best experience for our clients and workplace for our employees. AHF has a collaborative organizational structure where staff are accountable to multiple leaders.

Requirements

Medical Assistant Diploma or Phlebotomy Certification REQUIRED
Clinical Research experience REQUIRED
Bilingual in Spanish required

Responsibilities

Work as a part of a close-knit team to provide support to the Lead Coordinator and investigator to prepare and complete study visits.
Complete, maintain and process case report forms in compliance with good clinical practices.
Confirm that participants have signed all required consent forms before becoming involved in any aspect of the study.
Provide support in identifying potential study participants for investigator review.
Schedule all visits and procedures and providing instructions and dates to participants.
Schedule physician examinations with participants as needed.

Benefits

Comprehensive benefits to help our employees do and be their very best! These benefits are intended to enhance employee physical, financial, spiritual and professional health.

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