от компании (организации): АстраЗенека в городе (населённом пункте): Москва, Россия
в отрасли экономики "Производство, сельское хозяйство" → "Главный инженер"
с заработной платой: по договоренности
Вакансия № 27928370 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Вторник, 27 августа 2024 года.
Дата обновления вакансии № 27928370 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 № 27928370 может быть уже занята. Администрация сайта Работа в Москве и Московской области (МО, Подмосковье) приносит извинения за доставленные неудобства.
Требования к опыту работы:
1–3 года
Тип занятости:
полная занятость
График работы:
удаленная работа
Дополнительные сведения о вакансии: Study Safety Physician (Clinical Development Scientist)
Key responsibilities
- Develop scientific expertise on the clinical development for assigned compounds
- Lead or contribute strategic input to the clinical development plan
- Act as the clinical representative on Study Conduct Teams to ensure the clinical/scientific integrity of the study, and that trials are conducted effectively within budget- and time-constraints in order to deliver submission-quality data
- Develops and writes relevant sections of clinical documents such as study protocols, study procedure manuals, patient informed consent, written responses to IRB/Ethics Committees, clinical study reports and scientific publications
- In partnership with the Medical Monitor, provides clinical protocol training to internal and external groups (including at Investigator Meetings)
- Support of regulatory interactions (e.g. contributing to the creation of regulatory documents such as Investigational New Drug / Clinical Trial Applications, Regulatory Briefing Documents, and Investigational Brochures, support/attendance at regulatory meetings as required)
- Key contributor to the review of study data, interpretation of results and internal / external communication of study conclusions
- Work with and provide clinical support to the local teams, including late stage clinical development, regulatory and commercial experts, to deliver the overall needs of the medicine development strategy
- Must be able to interface seamlessly with other functions and groups, as well as external regulatory agencies to advance clinical assets effectively
Education and Experience
- BA/MS/PhD in Life Sciences with 3+ years relevant career experience
- If no degree in Life Sciences, must have significant experience in clinical development (>5 years)
- Therapeutic Area (Oncology) specific experience beneficial
Skills – General
- Strong written and verbal communication skills
- Excel and PowerPoint (PP) experience required
- Excellent organizational skills, including the ability to efficiently evaluate, prioritize and handle multiple changing projects and priorities
- The candidate should have experience in medical writing, enjoys troubleshooting, and has a problem solving mindset
- Ability to summarize complex information and present to varied audiences
Откликнуться на эту вакансию: Study Safety Physician (Clinical Development Scientist)
Предыдущая вакансия:
Вакансия № 27928369 на должность Руководитель проекта логистики от компании АО СмартРейс в городе (населенном пункте) Москва