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Naujas produktas žmonėms po insulto!

Lietuvos, Latvijos ir Baltarusijos rinkose įvestas naujausios kartos poinsultiniam periodui skirtas produktas NurAiDII MLC901. Efektyvumas įrodytas klinikinias tyrmais. Daugiau informacijos www.nuraid.lt

 

 

DOMINA NAUJI DARBO PASIŪLYMAI, NAUJI IŠŠŪKIAI IR GALIMYBĖS?!

 

KVIEČIAME PRISIJUNGTI PRIE MŪSŲ KOMANDOS!

 

 

ŠIANDIEN MES IEŠKOME:

 

               Pozicija: Medicinos atstovas

 

Pastoviai reikalingi medicinos atstovai su ne mažesne kaip vienerių metų patirtimi visuose Lietuvos regionuose. Darbas su etinių ir generinių farmacijos kompanijų OTC ir Rx produktais.

Gyvenimo aprašymą siųsti: info@armedika.lt

 

 

 

               Pozicija: Klinikinių tyrimų vadybininkas:

 

1. Šalis: KAZAKSTANAS, BALTARUSIJA

    Vieta: Nesvarbu


2. Šalis: RUSIJA
    Vieta: Nesvarbu

 

Job Description:


We are focused on the education, training, medical and pharmaceutical skills, bringing new outcomes for clinical trials.

 

This position plays an essential role in the company’s Clinical Operations Department. We are focused on multi-site Clinical Study management (Observational Studies, Phase I, II, III and IV trials) including start-up activities, project full management, interaction with Clinical contractors and/or vendors.
This person will be responsible for ensuring studies are performed in compliance with company procedures and all applicable GCP regulatory requirements and represents Quality in project teams in support of corporate development objectives. This person will also responsible for collaborating and supporting internal and external auditing plans and activities, training of employees and other staff as needed and in the development/maintenance of GCP related quality systems.
 

Duties and Responsibilities:

1. Ensuring compliance of clinical development activities and initiatives to applicable quality and regulatory requirements;
2. Developing, revising or assisting with study start-up activities, according quality system SOPs for GCP QA and Clinical Operations in compliance with applicable regulatory requirements;
3. Support outgoing project management activities for assigned studies/projects;
4. Participating in budget forecasting, planning for assigned project activities;
5. Providing expert GCP QA advice to Clinical Operations based on analysis and interpretation of updates to GCP regulations to assure best Clinical/QA practices;
6. Reporting significant and/or serious ongoing quality deficiencies to QA and Clinical Operations Management, Quality and Contracting Department (QCD) Management;
7. Develops, coordinates, conducts or supervises targeted training to Clinical Operations (e.g.: on SOPs), homecare/investigators/site staff (e.g.: GCP presentations for investigator meetings) and others at the company (e.g.: Regulatory Affairs);
8. Assists with oversight and management of consultants/vendors on as needed basis;
9. Assists with the organization, preparation, coordination, and documentation of regulatory inspections of investigator sites or Clinical Operations sponsor inspections;
10. Oversee, report study progress to the Clinical Operations Management and to the Sponsors;
11. Available as scheduled for customers and vendors questions during on-call hours;
12. Other assignments as directed by Clinical Operation Management.


Qualifications:

* Bachelor's in a scientific or health related field, Register Nurse licensed preferred;
* 2+ years experience in the Pharmaceutical or Biotechnology Industry;
* 5+ years in home care industry;
(Education and experience can be equivalent and negotiable).


Additional qualifications include:
• Excellent verbal and written communication skills, ability to work well in teams or independently and able to prioritize work, manage multiple projects while maintaining quality and advocate for compliance;
• Ability to deal with ambiguity, creative and pragmatic approach to problem solving and keeping things simple;
• Proven management skills, prioritize multiple projects and experienced QA advocate;
• Knowledge of medical and statistical practice/techniques, tools and terminology;
• Sensitivity of position requires a highly diplomatic and tactful individual with exceptional critical reasoning skills who is detail oriented;
• International clinical trial experience is preferred;
• This position also may require travel approximately 25-40% of the time.

If you would be available for this exclusive opportunity, please send your current CV at career@armedika.lt



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