Research Associate - CPT (Per Diem) at Parexel

Glendale, California, United States -

Full Time

Start Date

Immediate

Expiry Date

24 Apr, 26

Salary

26.0

Posted On

24 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Customer Service, Clinical Research, Phlebotomy, Data Entry, Problem Solving, Medical Procedures, Study Protocols, Participant Recruitment, Appointment Management, Safety Assurance, Quality Management, Documentation, Communication, Teamwork, Time Management, Adaptability

Industry

Pharmaceutical Manufacturing

Description

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. What you’ll do after training is completed (including but not limited): You will 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. Your Profile: Active CPT License in the state of CA is required Customer service experience in a fast-paced environment Experience working in a medical or clinical setting is highly preferred Comfortable standing and walking for a prolonged period of time B.S.+ in related life science field OR HS diploma/GED with relevant experience Hours/Shift - all shifts are onsite (no remote work) **please note this is not a full-time opportunity we are currently seeking per diem candidates (this role is not eligible for full time benefits). Required Training: two weeks working 40 hours a week Mon - Fri 8:00am to 4:30pm Post training requirements: 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. Additional availability is strongly recommended when possible. Can be scheduled up to 8 hours per day & 40 hours per week; but hours are not guaranteed and will vary based on business needs Base Pay Range: $20.00 to $26.00 per hour (this role is eligible for shift differentials) Actual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location. In addition to base salary, some roles may be eligible for participation in Parexel’s annual performance-based bonus plan, annual salary review and additional total rewards incentives. Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles. For all eligible employees, we offer market leading benefit programs including paid time off, 401k match, life insurance, health insurance, and other benefit offerings in accordance with the terms of applicable plans. EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

Responsibilities

The Research Associate will understand study protocols, recruit study participants, and conduct screening visits. They will also assist staff physicians and ensure participant safety throughout the study.