The Director of CMC Project Management will be responsible for the creation and execution of multiple complex CMC development and pharmaceutical operations plans. The Director will lead a team of project managers and will work closely with subject matter experts in chemical and formulation development, analytical development, technical operations and supply chain. Director will be responsible for comprehensive communication, including status reporting, risk management and escalation of issues to cross-functional stakeholders and Senior Management. Director will create processes to streamline project management and be accountable for project development and timelines for pharmaceutical development and pharmaceutical operations team members.
Required Skills
- Independently lead sub-teams.
- Work closely with Senior Management and project teams to develop goals, execution plans, budgets.
- Represent CMC on multiple cross-functional teams.
- Regularly interact with the following functions: Chemical Development, Formulation Development, Analytical Development, Technical Operations, Supply Chain, Regulatory, Quality, Clinical Operations.
- Conduct scenario planning and provide analysis and recommendations on development plans and periodically present to management to ensure alignment.
- Based on CMC strategy, (1) prepare and maintain detailed project timelines, (2) track the status of all ongoing development and manufacturing activities and regularly present project status updates, (3) ensure cross-functional alignment within the organization and with global partners
- Develop strong understanding of our strategy, pipeline, and capabilities, and actively leverage this knowledge to inform priorities for activities.
- Manage, develop, and mentor direct reports
Required Experience
BASIC QUALIFICATIONS:
- BS and 8+ years of pharmaceutical development, operations and CMC project management experience
OR
- M.S. and 6+ years pharmaceutical development, operations and CMC project management experience
OR
- PhD and 3+ years pharmaceutical development, operations and CMC project management experience
PREFERRED QUALIFICATIONS:
- Degree in organic, inorganic, analytical chemistry, biochemistry, chemical engineering
- Excellent communication skills, both verbal and written.
- Experience mentoring team members
- Working knowledge of ICH guidelines, module 3 sections, preparation of investigational new drug applications.
- Participation of new drug application preparation is a plus.
- Experience in developing, optimizing tools and systems for project management such as Smartsheet, Tableau, others
- Experience in establishing and leading governance for Portfolio Management to ensure appropriate projects prioritization and ranking.
- Ability to provide resource utilization/constraints overview,
- Financial experience/awareness (ROI calculations, depreciation..)
Akebia Therapeutics, Inc. is a fully integrated biopharmaceutical company with the purpose to better the lives of people impacted by kidney disease. The Company was founded in 2007 and is headquartered in Cambridge, Massachusetts. For more information, please visit our website at www.akebia.com.
Akebia is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.