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. Jump start your clinical research career today and apply to join Parexel as a Research Associate at our Baltimore, MD Early Phase Clinical Unit! Please note: this role is 100% onsite in Baltimore, MD and is not eligible for relocation or remote work. Key Accountabilities: Has detailed knowledge of the study protocols and acceptable performance of quizzes. Follows medical records procedure. Enters study participants in the study participant tracking system, ClinBase™, and study logs, maintains appointment calendars, and operates company information systems and computer programs. Conducts screening visits and study protocol specific study participant visits, assists staff physicians in assessment of concomitant medications, adverse events, lab results and other test results. Receives authorized sign-off to verify accuracy of all study participant visits. Prepares/monitors study supplies and stock levels in clinic/hospital. May assist in labeling, inventory and sending plasma samples. Problem solves study participant issues as they arise. Ensures basic study participant safety is provided Assists with Monitor visits (i.e., room set up, etc.). Identifies issues that need Sponsor approval and brings these to the attention of the CRC. Maintains supportive, flexible manner internally with management, coworkers/team members. Maintains and updates knowledge of Clinical Operating Guidelines and their proper application. Assumes appropriate role with study participants and caregivers. Assures quality and accuracy of source and CRF documentation. Complies with Quality Management (QM) department guidelines and performs corrections for QM, CRC and Monitor/Sponsor Representative in a timely manner. Exhibits professional demeanor at all times in external interactions with Sponsors/Sponsor Representatives. All other duties as assigned. Your Skills: Previous experience working in a clinical, medical, or hospital setting is required Ability to stand on your feet for long periods of time (this is not a desk job) Excellent interpersonal, verbal, and written communication skills The ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail. Comfortable collecting biological samples from patients (urine, blood, etc.) Your Profile: Customer Service experience Local to the Baltimore, MD area B.S/B.A. in related life science field (OR experience with high school diploma/GED) LVN/Phlebotomy preferred not required. Shift Requirements: Shifts: We are looking for candidates that can work: flex shifts (day, evening, overnight) Training schedule: first 4-6 weeks is training, and you will work 30-40 hours per week during that time. (typically shifts are 6:50am to 3:20pm ET) Minimum work requirements (after training is completed): 20 hours of availability per week (including 1 weekend shift) - please note this is not a full time role This position is not eligible for full benefits. 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. Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.