Description
My client, a global biopharmaceutical business are actively recruiting for an Associate Director, Clinical Development to join on a 12 month contract working remotely.
Key responsibilities include
- Program manager of various late stage oncology studies (including but not limited to oversight, issue management, and helping prepare business case around new studies)
- Leverage subject matter expertise to set up the operational plan for study in a strategic manner (i.e. what’s the best strategy for doing a study in new disease space)
- Partner closely with clinical development team to look at study design with foresight and strategic thinking, coming up with options and recommendations
- Manage stakeholders effectively through clear, concise communication
Experience required
- Subject matter expert of late stage oncology studies
- 3 – 5+ years as Global Study Lead
- Demonstrating desire for program management
- Experience in multi-dimensional role (role expands to more than just leading a study)
- Innovative thinking – demonstrates ability to think outside of the box and bring in new ways of working
- Strong partnership with stakeholders
- Ability to deliver key updates to senior leaders
- Effective oversight of Global Study Leads
- Capable of delivering complex story in simple, concise, digestible manner
- Clear, effective presentation style
- Effectively convey options to problems in order to efficiently identify a resolution

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