от компании (организации): Docs в городе (населённом пункте): Москва, Россия
в отрасли экономики "Медицина, фармацевтика" → "Клинические исследования"
с заработной платой: по договоренности
Вакансия № 14280829 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Среда, 21 августа 2024 года.
Дата обновления вакансии № 14280829 на сайте Работа в Москве и Московской области (МО, Подмосковье): Суббота, 21 сентября 2024 года.
Обращаем Ваше внимание, что на момент обращения к работодателю вакансия № 14280829 может быть уже занята. Администрация сайта Работа в Москве и Московской области (МО, Подмосковье) приносит извинения за доставленные неудобства.
Требования к опыту работы:
не требуется
Тип занятости:
полная занятость
График работы:
полный день
Дополнительные сведения о вакансии: Clinical Trial Assistant Moscow
Responsibilities:
Performs the role of Clinical Trial Assistant (CTA) supporting the Local Trial Manager and Site Manager to ensure optimal management of all documents with logistical and administrative tasks related to trial start-up, execution and closing of clinical trials .Performs regulatory document review and approval, including site specific Informed Consents.Ensures trial related activities are in compliance with GCO SOPs, policies and local regulatory requirements. May contribute to process improvement, training and mentoring of other CTA’s
Requirements: Partners with the LTM and Site Manager to ensure overall site management and adherence to internal SOPs, policies and local regulatory requirements.
2. Supports the local study team in performing site feasibility and/or country feasibility.
3. Maintains site level protocol information in Trial Management Systems (e.g. CTMS).4. In liaison with the LTM, ensures current versions of the required trial documents, trial-related materials and supplies are provided to the investigational site within required timeframes.
5. Where applicable, works with investigational site staff to ensure accurate/complete regulatory documents are in place to expedite IEC/IRB or Health Authority (if applicable) approval process.
6. Supports the LTM or, where applicable the SM, in providing the current and complete documents requested by the IEC/IRB and HA.
7. Supports the SM/LTM in collecting and maintaining all documents throughout the trial and post trial in both eTMF (i.e., IF/LAF sections) and paper files.
8. Distributes, collect, review, and track regulatory documents, agreements and training documentation.
9. Collects and tracks Financial Disclosure information at appropriate time points.
10. May contribute to process improvement including, but not limited, to representing functional area in process initiatives and contribute to optimization of daily processes.
11. May be assigned as a coach and mentor to a less experienced CTA.
12. Complies with relevant training requirements???????
Terms:A minimum of a BA/BS degree is preferred. Skills set corresponding with preferentially 2+ years relevant clinical trial experience or equivalent. Proficient in English language. Strong knowledge with MS Office (Word, Excel, Access, Outlook , Explorer and PowerPoint), Strong interpersonal and negotiating skills. Excellent organizational skills and the ability to collaborate and handle multiple priorities within a matrix environment. Perform activities in a timely and accurate manner. Proficient in the English language??????????????
Откликнуться на эту вакансию: Clinical Trial Assistant Moscow
Предыдущая вакансия:
Вакансия № 14280828 на должность Врач-кардиолог от компании ГБУЗ МО Раменская центральная районная больница в городе (населенном пункте) Котельники