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description de la société
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.
description de la fonction
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
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
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