Research Associate (Per Diem - Weekends)

Parexel•Baltimore, MD

1d•$20 - $22•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: Entry level Research Associate (per diem) Work Location: onsite in Baltimore, MD 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 Baltimore, MD 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.

Requirements

Proven customer service experience in a fast-paced environment
Background working in a medical or clinical setting
Comfortable with prolonged periods of standing and walking
B.S.+ in related life science field OR HS diploma/GED with relevant experience
CPT/Phlebotomy is highly preferred
First 4 to 6 weeks required to work 30 to 40 hours a week for training (day shift M-F 6:50am to 3:20pm)
Seeking candidates that can work 12-hour shifts on Saturday and Sunday
Bi-monthly attendance may be required for training sessions, unless there are no mandatory trainings to complete

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.
Ensure basic study participant safety is provided.
Assist with Monitor visits (i.e., room set up, etc.).
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.

Benefits

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.
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.

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