QUALIFICATIONS

Medical/scientific communication:

Planning and managing all kinds of medical/scientific projects according to GxP
Medical/scientific content production to any target audience including authorities
Marketing and communication planning and stakeholder analyses
Medical translations (lay or professional, between English, Danish and Swedish)

Medical publishing

News letters
Annual reports
Various other creative solutions

Scientific literature and research information

Understanding, gathering and translating complex scientific information to the defined target groups
Preparation of protocols, synopses, manuscripts and reports
Preparation and reviewing of authority documents
Translating complex scientific information to understandable "punch-lines"
A large number of peer-review articles in top medical journals
Over 50 medical compendia covering most therapeutic areas

Stakeholder management – the four step plan

Stakeholder identification (followed by a project initiation plan)
Stakeholder analysis (followed by a project plan)
Stakeholder matrix (followed by a project execution plan)
Stakeholder engagement (get the project done!!!)

Planning and teaching special courses and workshops at specialist and postgraduate levels

2500 hours of teaching at Medical University level
Planning and teaching special courses and workshops at specialist and postgraduate levels
6 years as course leader about pharmaceutical development at the The Danish Association of the Pharmaceutical Industry (Lif)
Countless presentations and lectures for R&D, sales, marketing, RA, pharmacovigilance etc.
Specific conference materials (e.g. posters, abstracts)

Regulatory affairs, quality affairs and drug safety

Regulatory affairs, quality affairs and pharmacovigilance guarantee the safety of the patients
Regulatory affairs is crucial in communication, marketing and advertising in the pharma industry
Knowing the "regs", how to interpret and follow them is a great advantage in every aspect of lifecycle management