от компании (организации): Parexel International в городе (населённом пункте): Москва, Россия
в отрасли экономики "Медицина, фармацевтика" → "Клинические исследования"
с заработной платой: по договоренности
Вакансия № 3094921 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Вторник, 24 сентября 2024 года.
Дата обновления вакансии № 3094921 на сайте Работа в Москве и Московской области (МО, Подмосковье): Среда, 25 сентября 2024 года.
Обращаем Ваше внимание, что на момент обращения к работодателю вакансия № 3094921 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:
полный день
Дополнительные сведения о вакансии: Associate Clinical Site Manager ii
At PAREXEL, we believe that the power to work independently and intelligently should be yours every day. Your ability to understand our clients’ needs and achieve quality results is critical to our reputation as one of the best clinical research organizations (CROs) in the world.
As a Clinical Site Manager (CSM) / Clinical Research Associate (CRA) within PAREXEL's Global Monitoring Operations Group, we support you with leading-edge technology, the highest caliber team members, and managers who know your strengths. If you're looking for flexibility and work-life balance, we're here to listen and help you move forward with your individual career path.
Responsibilities:
- Perform and arrange on-site observational visits (Qualification, Initiation, Monitoring and Termination) with appropriate support; apply judgment and knowledge to independently resolve site issues, questions and concerns.
- Help the local team in completing Clinical Trial Management Systems (CTMS) and study specific trackers
- Track, scan, code and apply naming convention and send documents to the relevant study e-CF Work In Progress (WIP) area and Central File (CF) area of PMED as per the Central File Maintenance Plan
- Learn to work in compliance with ICH-GCP Guidelines, applicable international and local regulations, PAREXEL SOPs, other PAREXEL and study specific procedures and requirements
- Learn to build relationships with investigators and site staff, including participation in calls with sites
- Understand the submission process for Site Regulatory Package (SRP) documents collection and follow-up
- Being involved in issue identification, follow-up and resolution.
- Be able to identify and evaluate potential quality issues.
Requirements: - Ability to interact professionally within a client organization with the support of manager or team members
- Flexible and positive attitude with respect to work assignments and new learning
- Ability to manage multiple and varied tasks with enthusiasm
- Attention to detail
- Willingness to work in a matrix environment and to value the importance of teamwork
- Strong computer skills including the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word
- Sound interpersonal, verbal, and written communication skills
- Sound proactive and problem solving skills
- Sense of urgency in completing assigned tasks and ability to assist others to meet study/ country deliverables
- Effective time management in order to meet daily metrics, team objectives, and department goals
- Shows commitment to and performs consistently high quality work
- Able to accommodate travel time requirements, according to tasks allocation/phase of the study assigned
- Willing and able to travel locally and internationally occasionally
Knowledge and Experience:
- Previous relevant work experience valuable
- Proficient in written and oral English and fluent in Russian
Education: - Educated to degree level (biological science, pharmacy or other health-related discipline preferred) or equivalent nursing qualification
Откликнуться на эту вакансию: Associate Clinical Site Manager ii
Предыдущая вакансия:
Вакансия № 3094919 на должность Администратор (инспектор службы безопасности) от компании Агентство ЛУКОМ-А в городе (населенном пункте) Москва