Вакансия: Clinical Research Associate (CRA)

Смотрите другие свежие вакансии популярной должности "Clinical Research Associate (CRA)".

Город, регион, страна: Санкт-Петербург, Россия (населённый пункт) места работы.

Смотрите другие свежие вакансии в городе (регионе) Санкт-Петербург

А также смотрите другие свежие объявления с работой на популярную должность "Clinical Research Associate (CRA)" в выбранном населенном пункте.

Компания: Parexel International (организация, фирма, ИП);

Логотип (бренд, торговая марка, эмблема) компании (организации, фирмы, ИП): Parexel International

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Дополнительное описание вакансии:
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success. As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You’ll also manage site quality and delivery from site identification through to close-out. As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. 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. If impact, flexibility, and career development appeal to you, Parexel could be your next home. Responsibilities: Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports. Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff. Protect patients. 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. Drive productivity. 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). Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability. Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification. Requirements: Site Management experience in clinical research, with understanding of clinical trials methodology and terminology. Ability to perform all clinical monitoring activities independently. Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline. Strong interpersonal, written, and verbal communication skills within a matrixed team. Experience working in a self-driven capacity, with a sense of urgency and limited oversight. A client-focused approach to work and flexible attitude with respect to assignments/new learning. 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). An honest and ethical work approach to promote the development of life changing treatments for patients. 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. Terms: Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe. As a member of our team, you’ll get to know your coworkers on a personal level. Have a question? A clinical research leader, project team member, technology “super user” or collaborator are a phone call away. 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. Management supports and encourages career growth through consistent performance discussions and evaluations. Whether your interest is to progress into a more senior level CRA role, into line management, Quality, Project Leadership or a variety of other positions, Parexel prides itself on career opportunities for our employees.

Вакансия № 1-18647938 относится к сфере деятельности: "Медицина, фармацевтика" » "Клинические исследования".

Вы можете перейти к просмотру актуальных предложений работы выбранного населенного пункта с учетом сферы деятельности вакансии № 1-18647938: "Медицина, фармацевтика в населенном пункте текущего места труда" » "Клинические исследования в населенном пункте текущего места труда".

Контакты работодателя / Смотреть детально...
(Переходите на веб-страницу сайта-партнёра «Центр Занятости Населения (электронный)» с вакансией № 1-18647938 на должность "Clinical Research Associate (CRA)" в городе (населенном пункте, регионе, стране) Санкт-Петербург, Россия, где находится телефон, Telegram, Skype, Viber, WhatsApp, E-mail, адрес работодателя "Parexel International")

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