Clinical Research Assistant

Alcanza Clinical Research•Jacksonville, FL

About The Position

Alcanza is a growing multi-site, multi-phase clinical research company with locations across multiple states and Puerto Rico and experience conducting Phase I–IV studies in several therapeutic areas. The Clinical Research Assistant supports Clinical Research Coordinators, the Site Manager, Principal and Sub Investigators, and other site staff in operating the clinical research site. Work is performed in compliance with GCP, ICH, HIPAA, FDA regulations, SOPs, and study protocols. The role includes clinical, laboratory, and administrative tasks that support assigned studies and site operations.

Requirements

High school diploma.
At least 1 year of administrative or clinical experience.
Proficiency with Microsoft applications, email, electronic health records, and web applications.
Ability to type proficiently at 40+ words per minute.
Strong organizational skills and attention to detail.
Well-developed written and verbal communication skills.
Well-developed interpersonal and listening skills; ability to work independently and with coworkers, subjects, managers, and external customers.
Ability to handle multiple tasks and adapt to changes in workload and priorities.
Professionalism, respect for others, self-motivation, and a strong work ethic.
High degree of integrity and dependability.
Ability to work under minimal supervision, identify problems, and implement solutions.
Ability to handle sensitive information confidentially and professionally in compliance with HIPAA guidelines.

Nice To Haves

One or more years of clinical research or clinical experience is preferred.
Bilingual English/Spanish proficiency is a plus.

Responsibilities

Assist with execution of assigned studies and site support functions in collaboration with the clinical research site team.
Under direction of the Site Manager/Director and Principal/Sub Investigators, support CRCs and other site staff in conducting study-related duties according to protocol.
Assist with basic screening of patients for study enrollment and patient follow-up visits.
Document information in source clinic charts.
Enter data in EDC and answer queries.
Obtain vital signs and ECGs; may perform blood draws.
Perform basic protocol-required laboratory procedures, including collecting blood specimens, operating a centrifuge, storing and shipping specimens, maintaining specimen accountability, and notifying couriers for specimen pickup.
Request and track medical record requests.
Assist the CRC with updating and maintaining logs and filing materials in charts.
Schedule subjects for study visits, send appointment reminders, and reschedule visits as needed.
Ensure study-related reports and patient results are reviewed promptly by the Research Coordinator and/or investigator.
Assist the CRC and/or Manager with study recruitment, patient enrollment, and tracking as needed.
Maintain confidentiality of patient, employee, customer, and company information and adhere to HIPAA guidelines.
Perform other duties as requested or assigned.