
Senior Director – Strategy & Delivery, Alzheimer's/Neurology
Posted May 2

Posted May 2
• Delivers comprehensive strategy and guidance for clinical trials, processes, and procedures.
• Serves as a Scientific Director or consultant as dictated by project needs.
• Functions as the primary senior-level liaison for clients.
• Engages in customer proposals, Requests for Information (RFIs), presentations, proposal defenses, and Steering Committees.
• Offers scientific and regulatory oversight along with project and therapeutic training to project teams.
• Collaborates with the Medical Writing department to prepare clinical development plans, protocols, investigator brochures, and medical/clinical reports as necessary.
• Coordinates the gathering of essential medical and scientific input from external experts, consultants, and advisors.
• Represents the company by attending industry events, delivering presentations, and participating in exhibition booths.
• Contributes to the creation of Standard Operating Procedures (SOPs), medical/scientific tools, training, and staffing requirements.
• Engages with senior management while providing scientific and medical insights to other departments as needed.
• Develops and implements strategic client engagement plans to foster long-term partnerships and promote organizational growth.
• Leads executive governance, addressing high-impact escalations and providing innovative solutions.
• Establishes and supervises the strategic direction for the execution of a complex and varied portfolio of clinical research projects.
• Maintains responsibility for the financial stability of a complex and high-value portfolio.
• Cultivates and leads a culture of innovation, accountability, and collaboration throughout the organization.
• Proven experience in delivering overall strategy and direction for clinical trials, processes, and procedures.
• Ability to act as a Scientific Director or consultant based on project requirements.
• Experience as a primary senior-level contact for clients.
• Involvement in customer proposals, Requests for Information (RFIs), presentations, proposal defenses, and Steering Committees.
• Capable of providing scientific and regulatory oversight along with project and therapeutic training to project teams.
• Skilled in collaborating with the Medical Writing department for the preparation of clinical development plans, protocols, investigator brochures, and medical/clinical reports.
• Responsible for coordinating the necessary acquisition of medical and scientific input from external experts, consultants, and advisors.
• Experience representing a company at industry events, speaking engagements, and exhibitions.
• Participation in the development of Standard Operating Procedures (SOPs), medical/scientific tools, training, and staffing requirements.
• Ability to interact with senior management and contribute scientific and medical insights to other departments.
• Serve as the senior-most operational leader and strategic advisor for top-tier clients.
• Develop and execute strategic client engagement plans for sustained partnerships and organizational growth.
• Oversee and influence high-stakes proposal development and bid defense strategies.
• Define and manage the strategic direction for the delivery of a complex and diverse portfolio of clinical research projects.
• Maintain accountability for the financial health of a complex and high-value portfolio.
• Inspire and lead a culture of innovation, accountability, and collaboration across the organization.
• Company car or car allowance.
• Health benefits including Medical, Dental, and Vision coverage.
• Company match for 401k contributions.
• Eligibility to participate in the Employee Stock Purchase Plan.
• Opportunity to earn commissions and bonuses based on individual and company performance.
• Flexible paid time off (PTO) and sick leave.
• Compliance with all applicable federal, state, and municipal paid sick time regulations.
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