Research Patient Recruitment Coordinator II / III (Chandler)

Arizona Liver Health•Chandler, AZ

28d•$60,000 - $90,000•Onsite

About The Position

Arizona Clinical Trials team is searching for qualified candidates to fill the Clinical Research Patient Recruitment Coordinator II / III position. This role is an integral part of the growing research team and serves as an educational resource for both patients and the patient recruitment team on clinical research eligibility and the benefits of new and innovative therapeutics.

Requirements

Experience and training in the conduct of clinical research and basic knowledge of medical terminology.
Thorough understanding of the principles of GCP and biomedical research ethics.
Thorough understanding of clinical research trials and their enrollment status and goals.
Ability to work independently with minimal day-to-day supervision.
Able to work well in a team.
Ability to consistently recruit for moderate to advance complexity trials correctly and efficiently.
Strong attention to detail and commitment to ensuring patient confidentiality.
Ability to multi-task and work in a fast-paced environment
Strong interpersonal, communication, and customer service skills, both verbal and written.
Must interact effectively with professional and administrative staff, sponsor, regulatory representatives, potential and current research subjects.
Strong organization, time-management, and leadership skills.
Advanced written and verbal communication skills.
Bachelor’s Degree in healthcare, biosciences, or other related field required.
Good Clinical Practice (GCP) certification required.
Must have valid documentation and authorization to work in the U.S. for any employer without sponsorship now or in the future.

Nice To Haves

Bilingual English and Spanish -- written and spoken is highly preferred
Experience with recruitment, data management and office administration is an advantage
Master’s Degree in healthcare, biosciences, or other related field preferred.

Responsibilities

Review standard of care (SOC) patients seen by providers who may qualify or be interested in participating in clinical trials.
Answer phone calls, social-media leads i.e. Facebook and/or other inquiries and use web-based systems such as Subject Well, Patient Navigator and/or sponsor provided portals to contact interested candidates.
Obtain HIPAA consent and enter subject data in electronic clinical trial management system
Evaluate participants through pre-screening and in-person interviews to ensure eligibility for the study.
Monitor, maintain, and find new study for screen fail subjects and those who have completed a study.
Contact potential subjects as per direction of providers.
Work alongside the Investigators, research nurses, research site managers, and clinical research coordinators to recruit new subjects into clinical trials and meet enrollment/exceed enrollment goals.
Assist research professionals with basic administrative and clinical procedures.
Provide all employees, research subjects, and interested candidates with an excellent service experience by consistently demonstrating professional decorum and knowledge of trials
Review and understand research protocols.
Contact past and potential participants who have expressed interest in clinical trials to determine eligibility through pre-screening
Provide study specific information not limited to study investigational product, potential side effects, duration of the study, compensation, etc.
Transfer pre-qualified candidates to research provider/investigator and delegated clinical research coordinator for final review and visit scheduling while ensuring transfer is successful.
Collaborate with community organizations and other external partners to facilitate recruitment.
Participate in weekend or after-hours recruiting events alongside providers and share results with patients.
Perform FibroScan and act as a general resource to patients and staff.
Participate in the training and orientation of new Research Recruitment Coordinators.
Maintain the company Research Board for actively enrolling studies. Actively review other informational documents and/or trial information portals.
Screen patient charts for actively enrolling studies.
Schedule appointments for eligible participants to attend the study.
Maintain accurate and complete participant records.
Attend research meetings and provide updates on recruitment activities.
Actively participate in the development of recruitment strategies.