от компании (организации): АстраЗенека в городе (населённом пункте): Москва, Россия
в отрасли экономики "Информационные технологии, интернет, телеком" → "Аналитик"
с заработной платой: по договоренности
Вакансия № 28881473 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Понедельник, 29 апреля 2024 года.
Дата обновления вакансии № 28881473 на сайте Работа в Москве и Московской области (МО, Подмосковье): Понедельник, 6 мая 2024 года.
Обращаем Ваше внимание, что на момент обращения к работодателю вакансия № 28881473 может быть уже занята. Администрация сайта Работа в Москве и Московской области (МО, Подмосковье) приносит извинения за доставленные неудобства.
Требования к опыту работы:
3–6 лет
Тип занятости:
полная занятость
График работы:
полный день
Дополнительные сведения о вакансии: Biostatistician
Major Duties and Responsibilities (including supervising others):
- Provides critical clinical programming support to projects.
- Interacts directly and independently with Data Management, Programmers, Clinical Development staff and management as a fully functioning member of the clinical programming team.
- Proactively keeps the manager updated on the status, programming accomplishments and criticality of any issues impacting the quality and timely delivery of statistical Programming outputs.
- Collaborates with external partners, ensuring partners have thorough understanding of expectations.
- Provide oversight for programming deliverables performed by service provider.
- Works independently, with minimal supervision from the manager.
- Actively solcits feedback from manager to address any issues and/or complex problems
- Provides accurate estimates on timelines.
- Leads in the development of analysis data set specifications.
- Independently implements and champions the use of standards and TA specific data listings, summary tables, and figures as specified in statistical analysis plan in the clinical study report.
- Develops robust, flexible SAS macro programs or modules that generate standard outputs and/or facilitate CDISC implementation.
- Ensures compliance of standards for all statistical programming assignments.
- Reviews and provides feedback on eCRF designs, eCRF annotations, DB structures, edit checks, SAPs and SPPs.
- Proactively offers and provides statistical programming and analytical skills that support clinical trial and/or TA projects and programs.
Requirements/Qualifications:
- Education: Degree with concentration in Life Sciences, Computer Science, Mathematics, Statistics or a quantitative/analytical field. Advanced degree preferred.
- Experience: A minimum of 5 years of clinical trial programming experience using SAS within pharmaceutical, biotechnology, and/or contract research organization industries.
- Special Skills/Abilities:
- Has acquired advanced SAS programming skills with proficiency in Base SAS, SAS/STAT and SAS/Graph. Able to develop standard SAS macros.
- Good working knowledge of CDISC guidelines. Good working knowledge of FDA regulations and GCP/ICH guidelines as related to clinical programming processes.
- General knowledge of medical terminology and clinical trials methodology.
- Excellent verbal, written, interpersonal and communication skills.
- Sound negotiation skills. Ability to mentor junior Statistical Programmers
- Fully understands data interoperability across and amongst the Clinical Data Management
- Application and all externally collected data.
Откликнуться на эту вакансию: Biostatistician
Предыдущая вакансия:
Вакансия № 28881472 на должность Аналитик торгового пространства / Мерчендайзер от компании Четыре Лапы в городе (населенном пункте) Жуковский