Qualified person responsible for information and publicity
Local contact person for pharmacovigilance
Regulatory affairs in belgium
The Pharmaceutical Affairs Associate Director acts as the Qualified Person Responsible for Information and Publicity (QP RIP) and is responsible for medical information and publicity in Belgium and Luxembourg
Job Summary
The Pharmaceutical Affairs Associate Director acts as the Qualified Person Responsible for Information and Publicity (QP RIP) and is responsible for medical information and publicity in Belgium and Luxembourg.
As Pharmaceutical affairs Associate Director, he (she) also steers locally the quality, regulatory and compliance activities within the affiliate and in collaboration with EU departments in accordance with Belgian, Dutch and Luxembourg laws and regulations.
The role involves fulfilling the employer designated Prevention advisor role in line with Belgium regulation and leading BeNeLux Compliance management.
Matching Summary
The Pharmaceutical Affairs Associate Director acts as the Qualified Person Responsible for Information and Publicity (QP RIP) and is responsible for medical information and publicity in Belgium and Luxembourg.
Skills & Requirements
Must-have
Qualified Person Responsible for Information and Publicity
Local contact Person for Pharmacovigilance
Regulatory affairs in Belgium
Medical information management
Promotional and medical material review
Quality assurance and distribution
Drug safety management
Nice-to-have
Scientific and business professionals
Highly motivated and collaborative
Passionate interest in fighting cancer
Experience in dynamic, lean environment
Cross-functional collaboration
Out-of-the-box thinking
Agile and strategic thinking
Key Requirements
Minimum of 10 years of pharmaceutical industry/biotech
Regulatory affairs in Belgium
Certified Prevention Adviser Level III
Fluent in English, French or Dutch
Oncology market experience
PharmD or PhD, or Bachelor of Science, Master’s in Science or Business