|
|
Реклама
|
|
|
(Senior) Clinical Research Associate
Career.ru
[+1]
- 29 апреля -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
International company is looking for Clinical Research Associate/Senior Clinical Research Associate. Responsabilities: Perform monitoring visits in accordance with the GCP/ICH Guidelines Initiating sites and observing recruitment, performing monitoring at... |
|
|
Clinical Research Associate
Career.ru
- 13 апреля -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
... of communication between Novartis and investigators for all clinical trail related activities to assure trials are conducted on time... ...medical and business knowledge Working experience in clinical research desired, or having demonstrated adequate level of proficiency within... |
|
|
Clinical Research Associate
Career.ru
[+1]
- 29 апреля -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
... and qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance to Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Ensure quality of data... |
|
|
Clinical Research Associate
Career.ru
[+1]
- 28 апреля -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
...Requirements: Degree in Medicine or a life science, nursing qualification or relevant experience; Preferably 1 year experience in clinical trials; Very good communication and presentation skills; Ability to take initiative and work independently; Competent English; Good... |
|
|
Clinical Research Associate
Career.ru
[+1]
- 19 мая -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
Our client-American Biotechnology Company is looking for Clinical Research Associate . Summary/Scope: Manage Investigative Site activities to ensure that subject safety is protected and that timely high quality data are collected in compliance with regulations... |
|
|
Clinical Research Associate
Career.ru
[+1]
- 12 мая -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
The world's leading pharmaceutical services organization is looking for people to position of Clinical Research Associate We are looking to recruit committed individuals to work in a busy clinical research department providing essential monitoring support... |
|
|
Clinical Research Associate (CRA)
Career.ru
[+1]
- 29 апреля -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
Global Pharmaceutical company is looking for specialist of clinical trials Requirements: Medical/Pharmaceutical/Similar education; minimum experience in clinical trials within CRO or Pharma company; good command of English; understanding of ICH GCP, FDA regulations, phases... |
|
|
Clinical Research Associate
Career.ru
[+1]
- 25 апреля -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
В настоящее время Исследовательская Группа Сервье занимает одну из лидирующих позиций в мире в области научных и клинических исследований (более 25 % оборота вкладываются в исследования). Наша приверженность исследованиям и открытиям является основой нашей деятельности... |
|
|
Clinical Research Associate
Career.ru
[+1]
- 28 апреля -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
..., lab certification etc.) • Coordinate study material (e.g. CRFs Clinical Trial Material {CTM}) shipment and receipt by study site • Accurately... ... Pharmacy degree, etc.); • 1-1,5 years experience as a Clinical Research Associate Level I; • Travel required; • Valid current passport required; • Fluent... |
|
|
Clinical Research Associate
Career.ru
[+1]
- 28 апреля -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
What are the most important duties? Periodically review clinical research sites, as directed by a project manager, and produce written reports in... ... and query resolution) Management and training of junior research associates What is the background of the ideal candidate (educational experience... |
|
|
Clinical Research associate
Career.ru
[+1]
- 25 апреля -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
Responsibility: The Clinical Research Associate for bioequivalent studies (CRA for BE) is responsible for all aspects of study management for assigned BE studies. These studies are conducted within the applicable standards, according to Good Clinical Practices... |
|
|
Clinical Research Associate, Moscow
Career.ru
[+1]
- 9 мая -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
PPD is a leading global contract research organization providing drug discovery, development and lifecycle management... ... is suitable for CRAs who have at least 1 year of experience. As a Clinical Research Associate your main duties will be: Perform and coordinate all aspects of the clinical... |
|
|
In-house Clinical Research Associate (IHCRA)
Career.ru
[+1]
- 18 мая -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
PRA International is a global leader in providing clinical research services to the pharmaceutical and biotechnology industries. With a reputation... ... in development today. Responsibilities: As an In-house Clinical Research Associate you will be working closely with the Lead CRAs and CRAs by providing support... |
|
|
Clinical Research Associates I - II
Career.ru
[+1]
- 12 мая -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
... of millions of people all over the world. Our current growth of Clinical Development Services (CDS) in Eastern European countries brings new... ... career development. At the moment we are looking for: Clinical Research Associates I - II. Location: Moscow As CRA you will be responsible for all aspects... |
|
|
Clinical Research Associate
Career.ru
[+1]
- 4 мая -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
Responsibilities: Initiate, monitor, close study sites in Russia and CIS countries according to Good Clinical Practice guidelines, Astellas’ standard operating procedures and local laws Ensure that study timelines are kept and that studies proceed according to agreed plans... |
|
|
Clinical Research Associate for bioequivalent studies
Career.ru
[+1]
- 3 мая -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
Responsibility: The Clinical Research Associate for bioequivalent studies (CRA for BE) is responsible for all aspects of study management for assigned BE studies. These studies are conducted within the applicable standards, according to Good Clinical Practices... |
|
|
Специалист по клиническим исследованиям / Clinical Research Associate (CRA)
Career.ru
[+1]
- 11 мая -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
Специалист по клиническим исследованиям (Clinical Research Associate). На контрактной основе. Требования к кандидату: Образование – высшее (медицинское или фармацевтическое) Опыт работы в области надлежащей исследований от одного года Знание Правил надлежащей... |
|
|
Clinical Research Associate
Career.ru
[+1]
- 19 мая -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
Clinical Research Associate Description: As a key member of the clinical operations team you will be at the forefront of clinical trials practice, implementing and monitoring trials, ensuring that sponsor and investigator obligations are met, and overseeing... |
|
|
Clinical Research Associate
Career.ru
[+1]
- 19 мая -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
Clinical Research Associate based in Moscow Clinical Research Associate with 2 years minimum monitoring experience in Oncology or Neurology. Based in Moscow, Russia PRA International is one of the best clinical development organizations in the world. We work... |
|
|
CRA/Clinical Research Associate
Career.ru
[+1]
- 29 апреля -
[ Сохранить ]
Сохранено
-
[ Подробности ]
[ Сохраненные вакансии ]
|
Москва
|
|
...GCP, company’s SOPs and applicable regulations.The responsibilities will also include negotiations with the investigator sites of clinical trials agreements and study budgets, obtaining and review of required documents from investigator sites. This position presumes full... |
|
|
Реклама
|