Associate Director Pharmaceutical Affairs BeNeLux
BeiGene, Ltd., Sauk Trail Beach, Wisconsin, United States
* Organization of trainings on pharmaceutical and compliance processes* Review of training material for commercial and medical teams* Evaluation of skills* Overseeing the training of medicinal representatives visiting doctors, pharmacists, and other healthcare professionals.**Prevention advisor role****:*** Fulfill the role of the employer designated Prevention advisor in line with the Belgium regulation* Overview
the legally required, repeated risk analysis to advise the employer on preventive protective measures* A minimum of 10 years of pharmaceutical industry/biotech in regulatory affairs in Belgium (and Lux is a plus)* Certified Prevention Adviser Level III* Fluent in English, French or Dutch (trilingual is a plus)* Oncology market experience strongly preferred* Experience in working in a dynamic, lean environment is preferred* In depth knowledge and understanding of the regulatory system and challenges and opportunities* Hands-on experience and successful track record in contacts with regulatory authorities* Demonstrated success and experience supporting product pre-launch, launch and post-launch* Demonstrate deep scientific knowledge* Demonstrated ability to translate strategic insights into practical, well-designed processes* Demonstrated ability to operate in matrix environment* Demonstrated cross-functional collaboration and out-of-the-box thinking* Agile, strategic thinking and ability to develop innovative global reimbursement/pricing strategies* Highly skilled in influencing cross-functional teams, including interfacing with key internal and external stakeholders and with scientific and commercial teams* Excellent interpersonal, oral and written communication skills, including ability to synthesize data and deliver a clear overview of market access strategy, opportunity and risks #J-18808-Ljbffr
the legally required, repeated risk analysis to advise the employer on preventive protective measures* A minimum of 10 years of pharmaceutical industry/biotech in regulatory affairs in Belgium (and Lux is a plus)* Certified Prevention Adviser Level III* Fluent in English, French or Dutch (trilingual is a plus)* Oncology market experience strongly preferred* Experience in working in a dynamic, lean environment is preferred* In depth knowledge and understanding of the regulatory system and challenges and opportunities* Hands-on experience and successful track record in contacts with regulatory authorities* Demonstrated success and experience supporting product pre-launch, launch and post-launch* Demonstrate deep scientific knowledge* Demonstrated ability to translate strategic insights into practical, well-designed processes* Demonstrated ability to operate in matrix environment* Demonstrated cross-functional collaboration and out-of-the-box thinking* Agile, strategic thinking and ability to develop innovative global reimbursement/pricing strategies* Highly skilled in influencing cross-functional teams, including interfacing with key internal and external stakeholders and with scientific and commercial teams* Excellent interpersonal, oral and written communication skills, including ability to synthesize data and deliver a clear overview of market access strategy, opportunity and risks #J-18808-Ljbffr