Medical affairs associate

22-10-2019 kampenhout
bedrijfsprofiel

IN2Pharma is a consulting company passionate about offering solutions in Medical, Regulatory Affairs and Quality Assurance projects to pharmaceutical and healthcare industry in Benelux. Our offices are located at “Hof ter Loonst” in Kampenhout.

They are looking to expand the team with a Medical Affairs colleague who has the ambition and potential to grow in our organization. All projects within IN2Pharma are worked on in small teams of 2-5 people and for some projects, you also work on site at the clients’ offices for 1 or 2 days per week.


jobomschrijving

Medical Affairs Associate with the ambition and potential to grow in a challenging organization? Take a look here!

As a Medical Affairs Associate, you will support the Qualified Person Responsible for Information and Publicity (QP RIP) in in establishing compliant promotional activities and materials for multiple pharmaceutical and healthcare companies in Benelux and contribute in medical writing projects:

  • Advice the Marketing departments of several MAHs in developing strong but compliant promo materials
  • Review and approve promotional activities in compliance with legislation on advertising and promotion
  • Obtain approval from Authorities for advertising to the general public, incl. TV or radio commercials
  • Install or improve local Healthcare Compliance SOPs
  • Upload or facilitate the preparation of the transparency file for betransparent.be or transparantieregister
  • Apply for Mdeon visum when inviting Healthcare Professionals (HCP) to a congress
  • Support in the establishment of contracts with HCPs and Healthcare Organizations (HCO)
  • Provide training on medicinal or healthcare products to sales representatives
  • Medical writing: expert reports, clinical evaluations, literature study
  • Answer medical questions on the MAH’s (medicinal) products

jouw aanbod

What do you need to be successful?

  • Level of education: Master degree in life sciences
  • A first experience with the review of promo material/activities, Sunshine Act, transparency disclosure
  • Familiar with good documentation practices and project management
  • Good communication skills in Dutch and English (both written and verbal)
  • Proficient with computer and Microsoft Office


Competencies that are an asset

  • Strong initiative, pragmatic and problem solver
  • Experience in other domains: medical writing, Regulatory Affairs or Pharmacovigilance
  • Accurate & efficient: concern for quality, compliance and consistency
  • Good communicator & team player

wat bieden wij?

  • A permanent full-time position with a competitive package and supplementary benefits
  • Challenging and alternating work environment at an exclusive location
  • Personal development opportunities by working closely together on challenging projects in different situations and for several pharmaceutical companies

overzicht
functie
technisch laborant (m/v)
jobtype
voltijds
contracttype
onmiddellijke vaste indienstname
referentie
CXRSP-85774
contact informatie
Anneleen Vanbuggenhout
anneleen.vanbuggenhout@cx.ausy.be 03 369 65 88
03 369 65 88