include understanding study protocols, performing required medical procedures, and actively recruiting study participants through various outreach methods. The role also involves conducting screening visits, assisting physicians with assessments, managing study supplies, and ensuring the accuracy of documentation.
Requirements summary
Candidates need proven customer service experience in a fast-paced setting and background experience in a medical or clinical environment, along with comfort standing and walking for prolonged periods. A Bachelor's degree in a related life science field or a High School diploma/GED with relevant experience is required, and CPT/Phlebotomy skills are highly preferred.
high schoolbachelor degreeCustomer ServiceData EntryAppointment SchedulingSource DocumentationMedical ProceduresParticipant RecruitmentParticipant SafetyAdverse Event AssessmentStudy Supply ManagementInformation Systems OperationScreening VisitsLab Result AssessmentStudy Protocol UnderstandingStudy Participant TrackingMonitor Visit AssistanceQuality Management Compliance
Job 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: 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.
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.
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.
Benefits
Life Insurance
Paid Time Off
Health Insurance
401k Match
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: 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 Hours/Shift - 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: First 4 to 6 weeks required to work 40 hours a week for training (day shift - 6:50am to 3:20pm) After training is completed: Minimum availability requirements: 16 hours of availability per week AND two 12-hour weekend shifts in a 4-week month OR three 12-hour weekend shifts in a 5-week month The actual number of hours scheduled and confirmed can vary between 0-40 hours a week, depending on business needs (hours are not guaranteed) Shift Details: Seeking flexible candidate that can work any shift (day, evening, overnight, & weekend) Bi-monthly attendance may be required for training sessions, unless there are no mandatory trainings to complete Base Pay Range: $20.00 to $22.00 per hour 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.™
