Responsibilities:
• Develop a comprehensive offering to support Allucent customers with DCT design from ideation through to protocol finalization that includes at least the following:
o Global regulatory and implementation strategy
o KPIs and results focused metric setup
o Roadmap and lead enterprise adoption models for design support o Endpoint selection amp; eCOA/eDRO strategy
o Incorporation of Patient and KOL Insights
o Protocol Design and Writing services
o Support with site identification and feasibility
o Maintain a library DCT-specific templates
o Develop/license/deploy tools and technologies to support DCT Design objectives
Requirements
• 10+ years of experience within life sciences consulting and/or clinical trial design (pharmaceutical, medical device, biotech, eClinical technology or contract research organization [CRO])
• BA or BS Degree, preferably in a life sciences discipline
• MD, MPH or PhD is preferred
• Proven track record of achieving or exceeding revenue goals and/or creating and implementing successful market offerings
• Knowledge of MS Office and business development software tools
• Experience with Customer Relationship Management (CRM) tools
• Experience with healthcare, mHealth and/or clinical research is desired
• Experience working in contracts/proposals/procurement at a eClinical, biopharma or CRO organization