Qualified person responsible for information and publicity
Local contact person for pharmacovigilance
Regulatory intelligence
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.
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.
He/she organizes a backing-up for the QP RIP role as applicable.
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 intelligence
Promotional and medical material review
Drug safety management
Compliance management
Risk management approach
Nice-to-have
Scientific and business professionals
Highly motivated, collaborative
Passionate interest in fighting cancer
Agile, strategic thinking
Cross-functional collaboration
Out-of-the-box thinking
Key Requirements
Minimum of 10 years pharmaceutical industry/biotech experience
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