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Research Associate Enrollment (Entry Level)

Parexel International Corporation

Multiple Locations

Parexel's Early Phase Clinical Unit in Baltimore, MD is hiring a Research Associate to join the day shift team. This is a great opportunity for a candidate that has some clinical knowledge to get their foot in the door and grow their career. Please continue reading to learn more:Key Accountabilities: Has detailed knowledge of the study protocols and acceptable performance of quizzes.Follows medical records procedure.Recruits study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.           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.Performs appropriate psychometric and efficacy testing according to study protocol.Receives authorized sign-off to verify accuracy of all study participant visits.Prepares/monitors study supplies and stock levels in clinic/hospital.Labels, inventories and sends plasma samples.Problem solves study participant issues as they arise.Ensures basic study participant safety is providedAssists 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.All other duties as assigned.Assumes appropriate role with study participants and caregivers.Attends and assists with start-up and flow sheet meetings.Completes Case Report Forms (CRF) in a timely manner.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. 

Skills:Strong interpersonal, written/verbal communication and organizational skills.Ability to stand on your feet for long periods of time (not a desk job)Ability to effectively manage time and multi-task.Demonstrated knowledge and skills necessary to provide care appropriate to the age and/or indication of the study participants.Ability to function well in a team environment.Computer proficiency required.

Knowledge and Experience:Prior clinical research experience, floor nursing, and/or psychiatric experience preferred.Experience assisting with patients in a hospital or clinical setting

Education:BS, BA in a related field or equivalent work experience

This role may be subject to government and/or customer requirements regarding vaccination against COVID-19 that are more stringent than Parexel policy.  Accordingly, successful applicants may need to be either vaccinated against COVID-19 or have an approved religious or medical exemption. Employment is contingent on disclosure of your COVID-19 vaccination status and, if relevant, proof of vaccination.

Job posted: 2023-01-31

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