от компании (организации): Kelly Services в городе (населённом пункте): Москва, Россия
в отрасли экономики "Медицина, фармацевтика" → "Клинические исследования"
с заработной платой: по договоренности
Вакансия № 11979553 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Среда, 2 октября 2024 года.
Дата обновления вакансии № 11979553 на сайте Работа в Москве и Московской области (МО, Подмосковье): Четверг, 14 ноября 2024 года.
Обращаем Ваше внимание, что на момент обращения к работодателю вакансия № 11979553 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: Clinical Project Manager
Primary activities:
- Takes overall responsibility for the study delivery in Russia
- Provides project’s milestones and deliverables oversight for up to 10 clinical studies with different types of funding depending on incoming study workload
- Provides functional oversight for contract CRAs during validation, initiation, routine, close-out monitoring activities; review of monitoring visits reports, proposes and follow-up the implementation of corrective and preventive actions by CRAs, provides feedback on performance if required
- Ensures that studies are performed in compliance with ICH/GCP, Company global standards, local SOPs, laws and regulations. Conduct quality co-monitoring visits
- Maintains a therapeutic area investigators database
- Continuously participates in relevant training courses to improve personal/professional skills, provides study- and GCP-specific training to CRAs, CTCs and/or relevant Company staff
- Participates in local, regional and global non-protocol related activities
- Cooperates with colleagues from other departments to support local product registration and approved promotion activities
- Reports on fraud or scientific/ethical misconduct as appropriate
- Contributes to development and improvement of departmental procedures and processes in the scope of the company’s effort towards continuous quality improvement
- Provides timely input and update of relevant clinical study databases depends on study period
- Serves in clinical trials as point of contact for internal and external stakeholders. Works internally with PV, Regulatory, and Global Medical Affairs to align on key decisions
- Works with external investigators, vendors, and contractors to ensure consistency across organization. Participates in knowledge generation across industry
The successful candidates will meet the following requirements:
- Master's Degree preferably in Medicine or equivalent Health Care related experience
- It is desirable that the candidate has not less than 5-6 years of experience in CR, including monitoring and project management
- Strong scientific and clinical knowledge, an understanding of clinical trial planning and management
- Fluency in English language
- Superior oral and written communication in an international environment
- Excellent project management and organizational skills
- Strong leadership skills (scientific and business), ability to lead across several dimensions simultaneously
- Ability to think strategically and objectively and with creativity and innovation
Company offers:
- Competitive compensation and benefit program
- Salary rate is under discussion
- Medical insurance
Откликнуться на эту вакансию: Clinical Project Manager
Предыдущая вакансия:
Вакансия № 11979552 на должность Специалист по логистике от компании АО «ОТИСИФАРМ» в городе (населенном пункте) Долгопрудный