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. Parexel comes along with an extensive induction program and ongoing training while following your individual career path. After training is completed, 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 solve 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. The role requires customer service experience in a fast-paced environment, being located near Baltimore, MD and comfortable commuting to the unit located at the MedStar Harbor Hospital, and being comfortable standing and walking for a prolonged period of time. A B.S.+ in related life science field OR HS diploma/GED with relevant experience is required. CPT/Phlebotomy is highly preferred. Hours/Shift - all shifts are onsite (no remote work). This is not a full-time opportunity; per diem candidates are sought (not eligible for full time benefits). Required training: First 4 to 6 weeks require working 30 to 40 hours a week for training (day shift - 6:50am to 3:20pm). After training, minimum availability requirements are 16 hours per week AND 2 -12 hour weekend shifts in a 4 week month OR 3 – 12 hour weekend shifts in a 5 week month. Actual hours scheduled can vary between 0-40 hours a week depending on business needs. Shift details: flexible candidate that can work any shift (day, evening, overnight, weekend). Bi-monthly attendance may be required for training sessions unless no mandatory trainings are scheduled.
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