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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.
Interested? Apply by sending your resume to email@example.com.
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 the review and approval of promotional activities and materials for multiple pharmaceutical companies in Benelux and contribute in pharmacovigilance projects.
Promotional material & activities:
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
Local Literature Review for the MAHs medicinal products
Risk Minimisation Acvtivities: agree with authorities and distribute RMA material
PV quality system set-up or maintenance: PV SOP's, gap analysis, compliance checks
Act as (back-up) Local Contact Person for pharmacovigilance
Provide PV awareness training to MAHs employees
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
what do we offer?
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