Clinical Research Associate - вакансия 767353

PRA International

Дата обновления: 14.10.2021

Город: Новосибирск

Категория: Медицина / Фармацевтика

Тип занятости: Не имеет значения



Текст вакансии:


Calling all Clinical Research Associates covering Novosibirsk region (any level of seniority). ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. As a Clinical Research Associate, you will be dedicated to one of our global Biotechnology clients who pride themselves on their quality and patient centric approach. They continue to challenge the status quo whilst ensuring the highest standards of compliance and acknowledging the importance of both global and local expertise. The Clinical Research Associate is ultimately responsible for the successful management of investigator sites and monitoring activities for assigned clinical studies throughout the trial lifecycle. Key responsibilities include: Full ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan. Developing effective relationships with investigator site staff to ensure that key clinical metrics are met. Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines. What do you need to have? Education: Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; Master's, PhD or MD degree; a licensed health-care professional (i.e., registered nurse, physician); or equivalent work experience required Skills: Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment. A working knowledge of ICH-GCP guidelines and local/international regulatory requirements. Experience in monitoring all trial components Strong communication skills Fluency in English and Ukrainian Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.




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