PLG is a global service provider in Life Sciences, dedicated to supporting patient access to safe and effective healthcare solutions. We deliver worldwide consulting and outsourcing services through the entire product life cycle. Our team is diverse, entrepreneurial, and committed to continuous improvement and innovation, and now we are looking for a Programme Director in the Regulatory Affairs and Operations Department to ensure a Global Regulatory Strategy for our clients.

Group 10
Responsibilities

  • Establish and Communicate Long-Term Strategy for clients’ programmes at PLG: Review high-level financial information and complete strategic reviews of resource capacity and capabilities to avoid delays, improve efficiency, ensure accuracy and timeliness of filings, and help the business stay in compliance.
  • Ensure a Global Regulatory Strategic Lead for our clients: Align regulatory activities with business or marketing strategies to provide overall direction to the client. This involves identifying important regulatory elements and describing specific steps and actions required to meet the regulatory strategy objectives. The strategy ensures regulatory compliance, business alignment, and operational efficiency, enhancing market competitiveness.
  • Manage and Lead the Team at PLG: Provide leadership and direction to the regulatory affairs team, ensuring clear definitions of required resources, both human and financial. Foster a collaborative and productive work environment.
  • Manage Client Relationships: Build and maintain strong relationships with clients, acting as the primary point of contact. Ensure client projects are handled efficiently and meet client expectations and deadlines.
  • Solve Client Issues: Proactively identify and resolve client issues, ensuring high standards of service and client satisfaction.
  • Review and Optimize Processes: Continuously review and optimize regulatory processes to enhance market competitiveness and ensure compliance.

Group 12
Experience

  • Bachelor’s degree or more in a Life Sciences-related field. A Pharmacy degree would be a plus.
  • 10+ years of experience in the role with references available from previous employers.
  • Experience in global RA strategies.
  • Good understanding of data and document management systems.
  • Proficiency in MS Office applications.
  • Organizational skills to help in managing multiple client accounts and ensuring the timely delivery of services.
  • Interpersonal skills are crucial for building strong relationships with clients and fostering trust.
  • The ability to work well within a team and autonomously ensures that client projects are handled efficiently.
  • Prioritizing different workloads and multi-tasking capabilities are necessary to meet client expectations and deadlines.
  • Attention to detail and process orientation help in maintaining high standards of service.
  • Flexibility and adaptability are important for responding to changing client needs and market conditions.
  • Knowledge of French and English.

Programme Director - Regulatory Affairs (RA) Department - VAF260

Apply