Acadia Pharmaceuticals Inc. logo

Director, Clinical Operational Excellence

Acadia Pharmaceuticals Inc.
Full-time
Remote friendly (San Diego, CA)
United States
$191,000 - $238,800 USD yearly
Operations

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Role Summary

Director of Clinical Operational Excellence will lead strategic initiatives that optimize and standardize clinical operations across global programs. This role drives continuous improvement, ensures regulatory compliance, and fosters a culture of quality and efficiency. The Director will design and implement process improvements, oversee training and SOP management, and apply data-driven insights to enhance clinical trial execution.

Responsibilities

  • Develop, lead and implement process optimization strategies for clinical operations to enhance efficiency, reduce costs, and ensure regulatory compliance through strategic leadership, process management and change enablement.
  • Lead Clinical Operations strategic planning sessions to align process improvement goals with long-term business objectives.
  • Establish mechanisms to identify, prioritize and resolve process issues/gaps within Clinical Operations; prioritize and implement process improvements through collaborative problem solving and effective communication.
  • Identify opportunities for improvement within existing operational processes and lead continuous improvement programs, applying methodologies such as Lean Six Sigma to drive measurable outcomes.
  • Track and report performance metrics to demonstrate impact of improvements.
  • Lead the production and reporting of operational excellence metrics to the Clinical Operations Leadership Team and key internal stakeholders, driving decisions based on data and analysis.
  • Ensure GCP compliance and data integrity through data-driven insights.
  • Oversee creation, maintenance and obsolescence of Clinical SOP/WI/Forms/Templates; direct work related to new process creation, training and rollout.
  • Manage QMS CAPAs, Deviations, and Document Change Controls (DCCs); support and manage audit findings and resolutions.
  • Monitor Clinical Operations training compliance; manage processes for ensuring that clinical operations and related CSPs using ACADIA processes are current with training and training documentation; may conduct training for small groups and participate in training sessions for CSPs
  • Manage the Clinical Operations Training Curricula; align curricula with applicable SOPs and ensure standardization across functions.
  • Serve as SME on regulatory requirements and industry best practices related to Clinical Operations processes and training compliance.
  • Collaborate with cross-functional teams to address training gaps and develop training materials; lead and conduct training sessions.
  • Drive change management initiatives to support adoption of new processes and systems; promote a culture of continuous improvement and quality mindset across Clinical Operations.

Qualifications

  • Bachelor’s degree in Life Sciences, Business, Engineering, or a related field; Master’s degree preferred.
  • Targeting 10 years of relevant progressive experience in clinical operations, with a focus on operational excellence and process improvement.
  • Demonstrated experience in leading process optimization initiatives and driving operational efficiencies in a global clinical trial setting.
  • Strong clinical operations and project management skills with expertise in process improvement methodologies (e.g., Lean, Six Sigma).
  • Previous management experience with demonstrated leadership capabilities.
  • Excellent communication and interpersonal skills, with the ability to work effectively across teams and with external vendors.
  • Proficiency in clinical operations systems and tools such as CTMS, eTMF, Veeva Vault platforms (Quality Docs, Clinical, Safety, RIM, Change Control, CAPA, Audits, Complaints, QRM, Supplier Management) and related platforms.
  • Must be able to travel on occasion.

Skills

  • Process optimization leadership in global clinical trials
  • Lean Six Sigma and other process improvement methodologies
  • Clinical operations systems proficiency (CTMS, eTMF, Veeva Vault, etc.)
  • Cross-functional collaboration and stakeholder management
  • Data-driven decision making and performance metrics

Education

  • Bachelor’s degree required; Master’s preferred (Life Sciences, Business, Engineering or related field)

Additional Requirements

  • Must be able to travel on occasion.
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