Anderen bekeken ook
Solliciteer nu

Country Approval Specialist (Submission Specialist)

  • SolCur
  • Kontich
  • Onbepaalde duur, Voltijds

Country Approval Specialist (Submission Specialist)

Functieomschrijving

Our customer is currently looking for a Country Approval Specialist to join the team in Belgium, working ideally from our office in Belgium however home based may be considered for an experienced candidate. As a Country Approval Specialist, you will:

  • Prepare, review and coordinate, under guidance, local regulatory submissions (EC, additional special national local applications if applicable, e.g. gene therapy approvals, viral safety dossiers, import license) in alignment with global submission strategy
  • Provide, under guidance local regulatory strategy advice to internal clients
  • Provide project specific local SIA services and coordination of these projects
  • May have contact with investigators for submission related activities
  • Key-contact at country level for either Ethical or Regulatory submission-related activities
  • Coordinate, under guidance, with internal functional departments to ensure various site start-up activities are aligned with submissions activities and mutually agreed upon timelines; ensures alignment of submission process for sites and study are aligned to the critical path for site activation
  • May work with the start-up CRA(s) to prepare the regulatory compliance review packages, as applicable
  • May develop country specific Patient Information Sheet/Informed Consent form documents
  • May assist with grant budgets(s) and payment schedules negotiations with sites.
  • Support the coordination of feasibility activities, as required, in accordance with agreed timelines
  • Enter and maintain trial status information relating to SIA activities onto tracking databases in an accurate and timely manner
  • Ensure the local country study files and filing processes are prepared, set up and maintained
  • Maintain knowledge of and understand SOPs, directives, and current regulatory guidelines as applicable to services provided

Profiel

To be considered for the role of Country Approval Specialist you should have:

  • Bachelor's degree
  • 0 - 2 years related experience or equivalent combination of education, training, & experience
  • Effective oral and written communication skills
  • Excellent interpersonal skills
  • Strong attention to detail and quality of documentation
  • Good negotiation skills
  • Good computer skills and the ability to learn appropriate software
  • Fluency in English and either Dutch or French
  • Basic medical/therapeutic area and medical terminology knowledge
  • Ability to work in a team environment or independently, under direction, as required
  • Basic organizational and planning skills
  • Basic knowledge of all applicable regional / national country regulatory guidelines and EC regulation

Aanbod

? Our customer hires only the best, develops ourselves and each other, and?recognises?the power of being one team.?They understand that you will want to grow both professionally and personally throughout your career, and therefore at this customer you will benefit from an award-winning learning and development?program, ensuring you reach your potential.??
? As well as being rewarded a competitive salary, our customer offers a benefits package based around the health and well-being of our employees.
? Our customer has?a?flexible working culture, where they truly value a work-life?balance.?They have grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. They are know as a?global?organisation?but with a local feel.?

Anderen bekeken ook

Kenmerken

Vereisten

  • Professionele Bachelor (Hoger Onderwijs Korte Type)
  • Nederlands, Engels

Aanbod

  • Onbepaalde duur
  • Voltijds
Bron: VDAB
Anderen bekeken ook

Ontvang per mail jobs op maat

Ontvang nieuwe 'Technisch consultancy' jobs in Antwerpen meteen in je mailbox.