About Acadia Pharmaceuticals
Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinsons disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimers disease psychosis and Lewy body dementia psychosis along with earlier-stage programs that address other underserved patient needs. At Acadia were here to be their difference.
Please note that this position can be based inSan Diego CA OR San Francisco CA OR Princeton NJ. Acadias hybrid model requires this role to work in our office three days per week on average.
Position Summary
The Director will lead Translational Sciences operations to support nonclinical toxicology and pharmacology/pharmacometrics clinical functions. The role will own and manage systems to facilitate clinical and nonclinical activities within the Translational Science department including internal and external vendor and contract management oversight and due diligence of agreements management and oversight of budgets and timelines. Interfacing with internal and external stakeholders is central to the role to ensure smooth and timely operational execution across Acadia programs.
Primary Responsibilities
Oversees the operational management of Translational Science project activities partnering with functional representatives to ensure delivery to plan and budget and in accordance to Program Team plans/commitments
Provides Translational Science team cross-functional project support to ensure seamless progress of activities across programs and with adjacent functions (CMC Clinical Development)
Identifies and manages vendors and consultants needed to complete Translational Science studies including associated contracts and budgets. Key partner for Finance Legal Vendor Management and Project Management Functions
Provides guidance to team members to objectively assess and resolve operational project issues to improve project effectiveness
Owner of operational Translational Science group meetings to ensure budgetary compliance across programs and co-ordination with CMC to ensure compound supply is met for seamless program progression
Partners with Head of Translational Sciences to maximize group efficiency and coordination anticipating potential hurdles and developing mitigation strategies
Other responsibilities as assigned
Education/Experience/Skills
Bachelors degree in life sciences or a related field. Targeting 10 years of progressively responsible experience in project operations and/or project management preferably supporting earlystage drug development. Experience managing team resources budgets and external vendors or consultants. preferably in a pharmaceutical or biotech environment. An equivalent combination of relevant education and experience may be considered.
Key Skills:
Experience managing cross-functional project activities and deliverables across complex programs
Strong understanding of the drug development process including pharmaceutical project management principles and GxP regulations (GLP GCP and related guidelines)
Deep experience managing operational aspects of early-stage drug development including academic and CRO-based contracts timelines and execution
Demonstrated operational management of Toxicology and Clinical Pharmacology activities
Proven experience overseeing vendors and consultants including performance and deliverables management
Ability to manage multiple priorities in a fast-paced cross-functional environment
Demonstrated experience in budget and resource planning tracking and management
Strong interpersonal negotiation and problem-solving skills with the ability to work effectively with business partners and leadership
Advanced proficiency in Microsoft Project Word Excel and reporting/tracking tools; ability to lead management of Translational Sciences systems and represent the function across tools
Self-motivated team player who thrives in dynamic environments with willingness to travel domestically and internationally
Physical Requirements
This role involves regular standing walking sitting and the use of hands for handling or operating equipment. The employee may also need to reach climb balance stoop kneel crouch and maintain visual verbal and auditory communication in a standard office environment and while working independently from remote locations. The employee must occasionally lift and/or move up to 20 pounds. This position requires the ability to travel independently overnight and/or work after hours as required by travel schedules or business needs.
#LI #SL-1
Required Experience:
Director
About Acadia PharmaceuticalsAcadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinsons d...
About Acadia Pharmaceuticals
Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinsons disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimers disease psychosis and Lewy body dementia psychosis along with earlier-stage programs that address other underserved patient needs. At Acadia were here to be their difference.
Please note that this position can be based inSan Diego CA OR San Francisco CA OR Princeton NJ. Acadias hybrid model requires this role to work in our office three days per week on average.
Position Summary
The Director will lead Translational Sciences operations to support nonclinical toxicology and pharmacology/pharmacometrics clinical functions. The role will own and manage systems to facilitate clinical and nonclinical activities within the Translational Science department including internal and external vendor and contract management oversight and due diligence of agreements management and oversight of budgets and timelines. Interfacing with internal and external stakeholders is central to the role to ensure smooth and timely operational execution across Acadia programs.
Primary Responsibilities
Oversees the operational management of Translational Science project activities partnering with functional representatives to ensure delivery to plan and budget and in accordance to Program Team plans/commitments
Provides Translational Science team cross-functional project support to ensure seamless progress of activities across programs and with adjacent functions (CMC Clinical Development)
Identifies and manages vendors and consultants needed to complete Translational Science studies including associated contracts and budgets. Key partner for Finance Legal Vendor Management and Project Management Functions
Provides guidance to team members to objectively assess and resolve operational project issues to improve project effectiveness
Owner of operational Translational Science group meetings to ensure budgetary compliance across programs and co-ordination with CMC to ensure compound supply is met for seamless program progression
Partners with Head of Translational Sciences to maximize group efficiency and coordination anticipating potential hurdles and developing mitigation strategies
Other responsibilities as assigned
Education/Experience/Skills
Bachelors degree in life sciences or a related field. Targeting 10 years of progressively responsible experience in project operations and/or project management preferably supporting earlystage drug development. Experience managing team resources budgets and external vendors or consultants. preferably in a pharmaceutical or biotech environment. An equivalent combination of relevant education and experience may be considered.
Key Skills:
Experience managing cross-functional project activities and deliverables across complex programs
Strong understanding of the drug development process including pharmaceutical project management principles and GxP regulations (GLP GCP and related guidelines)
Deep experience managing operational aspects of early-stage drug development including academic and CRO-based contracts timelines and execution
Demonstrated operational management of Toxicology and Clinical Pharmacology activities
Proven experience overseeing vendors and consultants including performance and deliverables management
Ability to manage multiple priorities in a fast-paced cross-functional environment
Demonstrated experience in budget and resource planning tracking and management
Strong interpersonal negotiation and problem-solving skills with the ability to work effectively with business partners and leadership
Advanced proficiency in Microsoft Project Word Excel and reporting/tracking tools; ability to lead management of Translational Sciences systems and represent the function across tools
Self-motivated team player who thrives in dynamic environments with willingness to travel domestically and internationally
Physical Requirements
This role involves regular standing walking sitting and the use of hands for handling or operating equipment. The employee may also need to reach climb balance stoop kneel crouch and maintain visual verbal and auditory communication in a standard office environment and while working independently from remote locations. The employee must occasionally lift and/or move up to 20 pounds. This position requires the ability to travel independently overnight and/or work after hours as required by travel schedules or business needs.
#LI #SL-1
Required Experience:
Director
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