Expire in: 22 days
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)
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