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ManpowerGroup Ukraine

Опубликовано 3 дня назад

Contracts & Grants Analyst

cityКиев

contactOlena Yurchenko

phone+38xxxxxxxxxx показать

sitehttp://www.manpowergroup.com

  • полная занятость
  • английский

Особенности вакансии

Знание языка

Английский язык

Вид занятости

Полная занятость

Специализация в медицине

Клинические исследования

International pharmaceutical company which conducts research and development activities related to a wide range of human medical disorders, including mental illness, neurological disorders, anesthesia and analgesia, gastrointestinal disorders, fungal infection, HIV/AIDS, allergies and cancer is looking for Contracts Grants Analyst

PRINCIPAL RESPONSIBILITIES:

  • support of the clinical research department
  • managing the end-to-end contract paperwork process
  • creation of requests and submission of the agreements on the appropriate authorization/ filling/ archiving tools
  • contract process quality control and sending executed contracts as appropriate to third parties
  • data entry and pull reports from tracking databases
  • collection and processing of information for determining the scope of services provided
  • work with financial documents, record keeping
  • communication with representatives of medical institutions, communication in centers (correspondence, calls, distribution, collection of documents)
  • work with calculations related to research, processing of accompanying financial documentation

POSITION SUMMARY:

  • Responsible for managing the end-to-end contract paperwork process
  • Responsible for contract process quality control and sending executed contracts and amendments as appropriate to third parties
  • Perform data entry and pull reports from tracking database(s)
  • Contact third parties to follow-up on contract and amendment execution
  • File and update on-site paper files as needed
  • Responsible for assuring the site, investigator and vendor payments are made as listed on the clinical trial agreement and in compliance with appropriate laws and guidelines
  • Responsible for creation of requests and submission of the agreements on the appropriate authorization/ filling/ archiving tools

EDUCATION AND EXPERIENCE REQUIREMENTS:

  • Bachelor's degree as minimum, at least 3 years' experience in clinical research/trials (SM/CRA, Clinical Trial Assistant, Start-up Specialist)
  • Experience in contracting (and in payments as a plus) in clinical research/trials
  • Excellent communication skills (both oral and written)
  • Fluency in English
  • Legal background is a plus, but not mandatory
  • Candidate also must have working knowledge of PCs (MS Office suite at a minimum)

If you are interested in our offer, please send in your CV in English.

Please note that we will contact only selected candidates.

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