Associate Director

Remote working opportunity for an Associate Director with Pharmaceutical Experience

Project management under the supervision of Research Directors, from setup to closure according to SOPs, including:

• Support Senior team members in preparing and contribute to writing proposals


• Build and maintain strong relationship and close collaboration with colleagues/peers in cross-country project teams and supervising third parties on a day-to-day basis within the study framework


• Management of external suppliers in line with negotiated quotes, incl. budget monitoring and update of internal hours and external costs


• Contribute proactively and knowledgeably to client project meetings to support the RD


• Day-to-day management of production including internal and external partners, and anticipating PM related issues, ensuring on-time delivery to internal and external clients


• Day-to-day client management in accordance with the Research Director


• Writing of study materials (screeners, guide / questionnaire, stimuli etc.) based on briefing


• Moderation of pilots/pre-tests, and interviews / focus groups


• Develop analysis plan based on briefing and prepare report templates


• Analyse qualitative and quantitative data


• Contribute to spotlight sessions with own perspective (brainstorms)


• Perform data quality checks (scripts testing, data, tables & reports) and provide useful and constructive feedback


• Write engaging and insightful reports including executive summary and recommendations based on spotlight session, join presentation to clients and demonstrate expertise


• Support RD/ sales team with business development activities, including client reach-outs, creds development and attending creds meetings


• Responsible for project compliance to Healthcare MR industry guidelines and Pharmacovigilance requirements, both industry-level and client-specific
  
  
  
  • Ensure that all staff on the project are currently compliant & up-to-date with all certification
  
  
  • Comply with internal and client compliance guidelines (e.g. AE, MR forms)
  
  
  • Ensure all AE reporting / special situation reporting in the course of the research, in line with client’s compliance
  
  
  
  


• Ensure document confidentiality and storage as per Clients’ requirements


• General knowledge sharing (not project specific) and participating in internal initiatives (e.g. innovation, training)