Работа и карьера
Открыть поиск
Закрыть поиск
Pharmacovigilance Scientist
20 Февраль 2020
Provision of Training Services
17 Март 2026
Senior Consultant, CBD COP17 Preparations
18 Март 2026
Head of Revenue & Promotion System
03 Март 2026
Rental Driver With/Without Vehicle
16 Март 2026
Translator/Interpreter – Farsi-Armenian
16 Март 2026
Intern for GIZ Armenia Country Office
18 Март 2026
Ֆինանսական մասնագետ
10 Март 2026
Administrative Assistant/Employment OR Service Contract
16 Март 2026
Logistician/Employment OR Service Contract
16 Март 2026
M&E Assistant /Employment OR Service Contract
16 Март 2026
Project Officer/Employment OR Service Contract
16 Март 2026
Թափքի Վերանորոգման և Ներկման Մասնագետ
16 Март 2026
Project Facilitator/Employment OR Service Contract
16 Март 2026
Տպագրիչ
27 Март 2026
Driver
06 Март 2026
Press and Public Information Officer
06 Март 2026
Security Assistant
06 Март 2026
ՀԱՐԹԱԿԻ ԲՈՎԱՆԴԱԿՈՒԹՅԱՆ ԲԱՐԵԼԱՎՄԱՆ ԾԱՌԱՅՈՒԹՅՈՒՆՆԵՐ ՄԱՏՈՒՑՈՂ ԸՆԿԵՐՈՒԹՅԱՆ ՆԵՐԳՐԱՎՈՒՄ
18 Март 2026
Cybersecurity Engineer
27 Февраль 2026
Interpreter
06 Март 2026
Բովանդակության Տարածման և Լսարանի Ներգրավման Մասնագետ
10 Март 2026
Store Manger
20 Февраль 2026
Concept Note and Call for Applications Research Academy on Human Rights Research in Armenia (April–October 2026)
03 Март 2026
Վարորդ-առաքիչ
03 Март 2026
Call for Proposals - Open Call for Ideas by Women-led NGOs
16 Февраль 2026
Team Assistant – Expert Services (f/m/d)
24 Февраль 2026
Բժշկական Ներկայացուցիչ
16 Февраль 2026
Հայտերի Ներկայացման Հրավեր "Բաց Գաղափարների Մրցույթ Կանանց Կողմից Ղեկավարվող Հասարակական Կազմակերպությունների Համար"
16 Февраль 2026
Բանվորուհի
03 Март 2026
Pharmacovigilance Scientist
| Компания: | FMD K&L |
|---|---|
| Локация: | Yerevan, Армения |
| Крайний срок: | 19 March 2020 |
ОПИСАНИЕ ДОЛЖНОСТИ:
FMD K&L Europe is seeking an enthusiastic candidate with medical background to fill the position of Pharmacovigilance Scientist within Pharmacovigilance Department. The basic function is to support different pharmacovigilance activities upon client request. All the candidates will be initially trained and supervised by their team leads for the first period of recruitment to be ready to start to work with a client.ОБЯЗАННОСТИ:
Product Literature Reviews- Perform routine Literature Review for detection of safety signals;
- Perform ad hoc comprehensive Literature Review for designated safety signal as requested;
- Review, analyze and develop conclusions based on sound scientific and medical knowledge and with reference to the existing product label;
- Provide a summary report of the review to the relevant SRL.
Case/ Case Series Reviews
- Review, analyze, synthesize Individual Case Safety Report (ICSR) and narrative line listing data, and/ or develop conclusions relative to:
a) Risk Management Plans (RMPs);
b) Scheduled Reports/Safety Updates (i.e. PSURs/PBRERs, DSURs).
Ad-hoc Requests/ Reports
- Post-submit Advisory Committee briefings.
Labeling Updates
- Review the AE data relative to a potential manufacturing deviation;
- Aggregate data reviews;
- Support signal evaluation and data review;
- Review safety database, including a detailed review of relevant individual records in support of signal evaluation;
- Search and summarize the background information required for signal evaluation from internal and external domain e.g. history of the issue, label, registration status, class effect, epidemiology data knowledge of disease;
- Prepare a summary slide stating outcome of routine literature;
- Where appropriate, prepare slides highlighting key aspects of relevant literature articles as related to potential signals;
- Prepare slides summarizing details of individual record report narratives with highlighted aspects relevant to potential signals;
- Prepare a summary slide stating whether as a result of review a signal has been detected and what the recommended action will be.
ТРЕБУЕМАЯ КВАЛИФИКАЦИЯ:
- Higher medical degree (Medical Doctor or Dentist);- At least 2 years of clinical work experience;
- English skills, including excellent reading and writing skills, advanced speaking skills;
- Ability to work full-time;
- Attention to details;
- Ability to multi-task;
- Knowledge of pharmacovigilance field and research is a plus.
ПРОЦЕДУРА ПОДАЧИ ЗАЯВОК:
Interested candidates are welcome to send their CV to: ***.**@******.*** indicating the position title ("Pharmacovigilance Scientist") in the subject line of the email. The Company appreciates all the interested candidates, however only the shortlisted candidates will be contacted for the upcoming interviews.Пожалуйста, четко укажите в своем заявлении, что вы узнали об этой возможности через Career Center, и укажите URL-адрес нашего веб-сайта - www.careercenter.am. Спасибо.
