от компании (организации): PRA International в городе (населённом пункте): Москва, Россия
в отрасли экономики "Медицина, фармацевтика" → "Клинические исследования"
с заработной платой: по договоренности
Вакансия № 2967643 добавлена в базу данных сайта Работа в Москве и Московской области (МО, Подмосковье): Воскресенье, 22 сентября 2024 года.
Дата обновления вакансии № 2967643 на сайте Работа в Москве и Московской области (МО, Подмосковье): Пятница, 15 ноября 2024 года.
Обращаем Ваше внимание, что на момент обращения к работодателю вакансия № 2967643 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: Senior Contracts and Grants Analyst
As a top five CRO, we have worked on 100+ marketed drugs across several therapeutic areas and conducted the pivotal or supportive trials that led to FDA and/or international regulatory approval of 45+ such drugs.
At PRA Health Sciences, providing innovative solutions for our clients is what we do. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.
At PRA, borders do not create boundaries. PRA’s success is dependent upon our ability to attract and retain a talented team of diverse professionals. Our growing workforce is comprised of over 10,000 employees, spanning 13 time zones across six continents and who speak more than 30 languages – yet operate in unison as one worldwide PRA community.
Summary:
Responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials. Provide support to the clinical team in the pricing, planning, execution and control of grants and contracts.
Responsibilities:
- Responsible for analyzing contract requests/needs from operating companies and translating into appropriate contracts/budgets for company sponsored and investigator initiated clinical trial agreements and other relevant legal documents as they relate to various clinical projects.
- Provide specialized support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required
- Analyze investigator grants for fair market value aligned with regional knowledge and grant pricing guidelines, and based on adequate scope of work, clinical trial protocol and other clinical trial information. Participate in and/or lead the approval escalation of grants as appropriate.
- Determine potential needs for contract amendments and manage amendment lifecycle.
- Ensure that contractual terms and provisions are in compliance with corporate process, systems, and strategies.
- Work with the global team as necessary to review and analyze contractual terms and conditions in order to reach acceptable language. Assess risks of budget and legal provisions in conjunction with members of the global team and support functions and communicate such to stakeholders. Liaise with global management, Healthcare Compliance, Risk Management, Privacy and other stakeholders to obtain guidance and escalate issues as appropriate.
- Assume responsibility for all aspects of legal document and metrics tracking.
- Adhere to SOPs, ethics and departmental compliance as determined by CDO management as well as operating companies, corporate and QA guidelines. Ensure familiarity with departmental and corporate processes including but not limited to the relevant processes associated with contracts and grants and operating companies
- Work proactively to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites.
- Comply with requests from QA and auditors.
- Mentor and train new contract coordinators and analysts
Qualifications:
• Bachelor’s degree in appropriate scientific or business disciplines
• 3- 5 years experience and/or equivalent competencies in legal/ pharmaceutical industry/clinical research
• Must have a working knowledge of the clinical development process with 2 years of negotiation and contract experience
• Excellent communication skills (both oral and written| Russian and English)
• Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, etc.
• Familiarity with clinical research processes
• Ability to work effectively in cross function teams
Откликнуться на эту вакансию: Senior Contracts and Grants Analyst
Предыдущая вакансия:
Вакансия № 2967640 на должность Офис-менеджер от компании АБ-МАРКЕТ в городе (населенном пункте) Москва