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The Director Process Management will be accountable for overseeing and optimizing clinical trial supply management and protocol deviation management processes within Global Clinical Operations (GCO). The Director of Process Management will be a senior leader with expertise in process design leading complex projects and operating effectively within a matrix organization.
The responsibilities listed below outline the scope of the position. The application of these tasks may vary based upon evolving business needs.
As the Global Process Owner for assigned processes lead the design maintenance and continuous improvement of end-to-end clinical processes. Ensure these processes are well defined comply with regulatory requirements are aligned with GCOs strategies implement innovative approaches being developed in the industry and support effective work. Ensure that written standards are developed and maintained as needed to support the process and that written standards can be clearly understood by end-users. Provide necessary information and training to help users understand and implement these processes effectively.
Define and implement process oversight strategy with key performance indicators in-process controls management monitoring and end-user feedback. Establish benchmarks and conduct periodic review of performance metrics to ensure effectiveness efficiency and compliance. Report process health and compliance to the relevant stakeholders proactively and take appropriate measures where deficiencies are identified.
Influence and engage with the organization by building a strong network with stakeholders partners and subject matter experts to understand their drivers and needs along with broader organizational goals. Use these insights to craft alignment drive meaningful change and improve end-user experience.
Define and manage process change roadmaps aligning priorities with system updates and innovations to address evolving business needs manage risks or interdependencies and implement improvements at scale.
Lead strategy planning execution and implementation of process change projects ensuring improvements are achieved through a combination of process-people-system solutions. Partner with subject matter experts and support roles to deliver a comprehensive solution package that includes the end-to-end process itself written standards training communication change management implementation and monitoring plans.
Maintain current knowledge of global regulations and guidance global regulatory expectations regulation intelligence and industry standards pertaining to the assigned processes. Proactively assess impact of any new regulations on assigned process and ensure ongoing compliance.
Proactively educate themselves in evolutions and innovations across the industry and evaluate how they could positively benefit the effectiveness efficiency or compliance of the process. Develop and align proposals with the appropriate stakeholders to drive process innovation that is aligned with GCOs strategic priorities and stakeholder needs.
Maintain personal readiness to respond to internal audits and regulatory inspections be the point of contact and interact with inspectors and provide expert advice to respond to audit observations.
Represent GSK in external forums to influence the external ecosystem in shaping industry-leading practices and development of innovative methodologies
Bachelors degree in Scientific discipline.
Extensive experience in Pharmaceutical or Biotech industry working in Clinical Operations Operational Excellence or a related field.
Proven experience in designing and managing clinical operations processes such as clinical trial supply management and protocol deviation management and knowledge of ICH/GCP and global regulatory guidelines for drug development and approval processes.
Experience leading major projects to completion and driving cross-functional improvements.
Experience in strategic and critical thinking problem solving influencing and decision-making.
Demonstrated a forward-thinking and visionary approach to modernizing clinical processes and leveraging technology to drive efficiency and innovation
Demonstrated experience in matrix team leadership to deliver results.
Demonstrated cross-functional collaborator with experience in building networks of partners and stakeholders and broadly engaging with expert communities.
Experience in effective communication with ability to communicate and influence.
Advanced degree in Scientific discipline
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Why GSK
Uniting science technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.
People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.
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