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Management supports and encourages career growth through consistent performance discussions and evaluations. Our clinical research teams meet regularly to have discussions in an open environment, allowing our team members to share their expertise and promote learning within the team. Have a question? A clinical research leader, project team member, technology "super user" or collaborator are a phone call away. As a member of our team, you ll get to know your coworkers on a personal level. Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe.
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This relocation requires a minimum of a 2 year commitment living in the United States.Minimum of one year experience as a Parexel employee.
#I itrain hard kew gardens trial#
Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.An honest and ethical work approach to promote the development of life changing treatments for patients.The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).A client-focused approach to work and flexible attitude with respect to assignments/new learning.Experience working in a self-driven capacity, with a sense of urgency and limited oversight.Strong interpersonal, written, and verbal communication skills within a matrixed team.Bachelor s or equivalent degree in biological science, pharmacy or other health related discipline.Ability to perform all clinical monitoring activities independently.Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.On your first day we ll expect you to have: Monitor the completeness and quality of Regulatory Documentation and perform site document verification. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s). Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports. If impact, flexibility, and career development appeal to you, Parexel could be your next home. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. You can anticipate less travel and a lower protocol load in comparison to industry peers. You ll also manage site quality and delivery from site identification through to close-out.Īs a CRA, Parexel will offer you world class technology and training catered to your individual experience. As the clinical sites sole point of contact, this includes addressing and resolving site issues and questions. CRA s are accountable for using their expertise to build and maintain the site relationship and ensure they re set up for success.
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At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor.