CLINICAL OUTCOMES MANAGER manages the collection and analysis of clinical outcomes data to develop clinical process improvement initiatives. Oversees staff who gather data on performance metrics and facilitates the review of clinical program effectiveness. Being a CLINICAL OUTCOMES MANAGER provides advanced analyses and reports on clinical outcomes data. Evaluates and summarizes patient data to ensure that care is provided in accordance with clinical guidelines and organizational standards. Additionally, CLINICAL OUTCOMES MANAGER identifies areas for improvement and assists leaders/physicians in developing strategies to improve performance. Requires a bachelor's degree in nursing or healthcare related area. May require a Registered Nurse (RN) license. Typically reports to a director. The CLINICAL OUTCOMES MANAGER typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. To be a CLINICAL OUTCOMES MANAGER typically requires 3+ years of managerial experience. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. (Copyright 2024 Salary.com)
The Phlebotomist (Clinical Research Assistant) is responsible for assisting the research coordinator and other staff with completing protocol procedures and processing laboratory samples for shipment. Promote good clinical practices (GCP) in the conduct of clinical investigations. All duties carried out by the research assistant are done in accordance with company policies, SOPs, GCP, and applicable local, state and federal regulations.
Primary Responsibilities
· Perform medical diagnostic tests such as electrocardiograms, blood pressure checks, etc.
· Collect and process blood and urine samples per protocol requirements.
· Professionally interact with subjects, visitors, staff, and other healthcare professionals.
· Maintain laboratory inventory.
· Sanitize and stock treatment rooms and exam rooms.
· Dispose of and replace biohazard waste in lab and exam rooms per OSHA requirements.
· Perform administrative tasks as needed.
· Maintain timely source documentation.
· Complete all monitor, sponsor and lab queries in a timely manner.
· Accurate and timely entry into CTMS.
· Other duties and responsibilities as assigned or directed.
Minimum Qualifications:
· High School Diploma
· Certified Medical Assistant or Phlebotomist preferred
· At minimum 2 years experience in phlebotomy
Additional skill set:
· Strong motivational skills and abilities – promoting a team-based approach
· Strong interpersonal and communication skills, both verbal and written
· Strong organizational and leadership skills
· Goal oriented
· Ability to maintain a professional and positive attitude
· Ability to communicate in a clear and professional manner
· Adhere to GCP
· Attention to detail and accuracy in completing tasks
· Strong ability to multi-task
· Experience drawing blood and preparing samples for testing.
Who We Are?
Segal Trials, founded in 1998, is a privately held network of five research sites throughout South Florida, conducting phase I-IV research trials with a primary emphasis on psychiatry, neurology, addiction, insomnia, general medicine, vaccinations and more. With a team of over 150 professionals, Segal Trials remains agile and competitive.
Segal Trials is regarded as an innovator and a leader in the advancement of medicine with a strong dedication to the community it serves by spreading awareness about clinical trials as a potential care option.
Why Segal Trials?
When working at Segal Trials, you will be surrounded by passion, diversity, and likeminded individuals who are striving in the pursuit of excellence. We will foster your continued success and you will begin making a difference on your very first day!
For more information, visit www.segaltrials.com
Job Type: Full-time
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Work Location: In person
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