Research Associate - CPT (Per Diem)

Parexel•Glendale, CA

12d•$20 - $26•Onsite

About The Position

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Job Title: Research Associate - Certified Phlebotomy Technician License Required Work Location: onsite in Glendale, CA Parexel Early Phase Clinical Unit supports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and “first in human” trials are the first step in testing these novel treatments in humans. At Parexel Glendale, CA unit our highly trained and skilled Research Associates are crucial to ensuring the successful completion of Phase I trials. This is a great role for anyone that aspires to be an enrollment specialist, clinical research coordinator, or eventually manager. Parexel provides a great system of support to help you grow and advance your career internally. Parexel comes along with an extensive induction program and ongoing training while following your individual career path.

Requirements

Active CPT License in the state of CA is required
Customer service experience in a fast-paced environment
Comfortable standing and walking for a prolonged period of time
B.S.+ in related life science field OR HS diploma/GED with relevant experience
Employees must provide, at minimum, full-day availability to work any shift between 5:00 AM and 12:00 AM three days a week, with one of those days being Sunday.

Nice To Haves

Experience working in a medical or clinical setting is highly preferred
Additional availability is strongly recommended when possible.

Responsibilities

Understand study protocols and be able to complete required medical procedures.
Recruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.
Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs.
Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results.
Prepare/monitor study supplies and stock levels in clinic/hospital.
Label, inventory, and send plasma samples.
Problem solves study participant issues as they arise.
Ensure basic study participant safety is provided.
Assist with Monitor visits (i.e., room set up, etc.).
Identify issues that need Sponsor approval and bring these to the attention of the CRC.
Maintain and update knowledge of Clinical Operating Guidelines and their proper application.
Assume appropriate role with study participants and caregivers.
Assure quality and accuracy of source and CRF documentation.
Comply with Quality Management (QM) department guidelines and perform corrections for QM, CRC and Monitor/Sponsor Representative in a timely manner.