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Новые вакансии в Ярославле
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Информация для пользователей и размещающих вакансии компаний » |
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Clinical Research Associate , требуется
Вакансия № 2306 Опубликована 29.04.10 15:00 Просмотров 519
Условия работы |
| Зарплата: |
договорная |
| График работы: |
Полная занятость |
| Место работы: |
На территории работодателя |
Требования к кандидату |
| Возраст: |
от 18 до 60 лет |
| Пол: |
Не важно |
| Образование: |
Не важно |
| Иностранный язык: |
Не важно |
| Опыт работы: |
Не менее 2 лет |
| Опыт работы, навыки, должностные обязанности: |
Responsibilities : Perform feasibility studies as requested Conduct pre-study and study initiation visits Ensure completeness, accuracy and submit regulatory and ethical submission documentation as appropriate Accurately maintain Investigator Site File Report findings at pre-study and initiation visits in site visit report Provide input into the design of protocols CRFs and monitoring plans Assess, monitor and train study site staff if required for protocol adherence Conduct monitoring to include Source Document Verification (SDV), site file maintenance and CTM accountability to a standard that allows mentoring and coaching of other CRAs Frequent and complete communications with study site Generate written correspondence with study sites Prepare concise reports of monitoring visits Provide all site related study documentation for filing into the Trial Master File (TMF) Demonstrate competence in query resolution Complete final study termination visit report Maintain close-out activities in compliance with regulatory requirements Requirements: Excellent oral and written communication skills Good planning and organizational skills with effective time management Excellent interpersonal skills Initiative and problem solving skills Ability to work logically and methodically Through understanding of clinical research principles and process Good understanding of FDA and /or EU Directive regulations, ICH Guidelines and local regulatory requirements Medical Doctor (MD) degree or Pharmacist (MSPH, PharmD, PhD, or equivalent Pharmacy degree, etc.) and with a minimum experience of one year as a Clinical Research Associate Level I, OR A minimum four-year college curriculum with a major concentration in biological, physical or health studies and a minimum experience of two years as a Clinical Research Associate (or one year as a Clinical Trials Associate and one year as Clinical Research Associate), OR Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree preferred) and a minimum experience of two years as a Clinical Research Associate Level I Travel required Valid current passport required Driving license required Fluent in the local languages of the countries under responsibilities and proficient in both spoken and written English Conditions: The company is offering competitive compensation & benefit program Salary rate is under discussion Insurance Opportunity of professional growth |
Контакты работодателя |
| Компания: |
Worldwide Clinical Trials
kazan.hh.ru
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| Контактное лицо: |
Worldwide Clinical Trials |
| Телефон: |
Не указано |
| E-mail: |
Не указано |
| ICQ: |
Не указано |
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