Clinical Trials Assistant (CTA) / Ассистент по клиническим исследованиям

Вакансия № 19470149 от компании IQVIA на Электронной Службе Занятости Населения Москвы.

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☑ Основной блок:

Опыт работы: не требуется.

Тип занятости: полная занятость.

График работы: полный день.

Зарплата: по результату собеседования.

Примерное место работы: Россия, Москва.

☑ Актуальность объявления:

Это объявление № 19470149 добавлено в базу данных: Четверг, 13 февраля 2025 года.

Дата его обновления на этом интернет-ресурсе: Воскресенье, 16 марта 2025 года.

☑ Статистика предложения работы № 19470149:

Прочитано соискателями - 40 раз(а);
Отправлено откликов - 0 раз(а);

☑ Репутация компании "IQVIA":

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☑ Подробности о вакантном месте:

Dear candidates, please apply with CV in English.

Join us on our exciting journey!

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.

At IQVIA, we know that meaningful results require not only the right approach but also the right people. Regardless of your role, you’ll have the opportunity to play an important part in helping our clients improve patient healthcare. You can drive your career at IQVIA and choose the path that best defines your development and success. With exposure across diverse geographies, capabilities, and vast therapeutic and information & technology areas, you can seek opportunities to change and grow without boundaries.

Do you want to contribute to the improvement of the global healthcare? Are you looking for a starting point in clinical research?

This is why Clinical Trials Assistant role is here for you!

WHAT WOULD BE YOUR ROLE:

Act as a central contact for the team for assigned project communications, correspondence and associated documentation.
Assist colleagues with accurately updating and maintaining systems that track site compliance and performance within project timelines.
Support the preparation, handling, distribution, filing, and archiving of clinical documentation and reports.
You may accompany Clinical Research Associates on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.

WHAT SKILLS & KNOWLEDGE ARE IMPORTANT TO HAVE:

Background: Bachelor or Masters Degree in Life Science will help you to deal with specific language of clinical trials and medical terminology. We appreciate awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
English language: fluent English is essential for communication within international environment at IQVIA.
PC skills: You should be able to work with Microsoft Word, Excel and PowerPoint and quickly get familiar with specialised software of IQVIA.
Working experience: previous experience in clinical trials area or general administrative role will be an asset.
Planning & multitasking: we will assign you with several projects at a time. Therefore, you will have a lot of urgent tasks to do.
Attention to detail & accuracy: behind each document is a real patient. You should keep a sharp eye on every detail of the document to ensure compliance with all procedures and regulations.
Collaboration: we do expect you to establish and maintain effective working relationships with coworkers, managers and clients.

Equivalent combination of education, training and experience would be also sufficient for the role.

WHAT WE HAVE TO OFFER:

We put special emphasis in offering the best training opportunities and fostering personal development. Our culture is based in improving the well-being of our employees, both at professional and personal levels. We offer flexibility, recognition and rewards as well as an attractive salary.

Please, submit your CV in English.