Associate Director, Clinical Process Learning

Desired Skills: LMS management,GCP/ICH,FDA/EMEA,and GCP-standards.

PE Global is currently recruiting for an Associate Director, Clinical Process Learning for a leading multinational pharma client based in London.

This is an initial 12 months contract position.

£550-£650/day depending on experience via Umbrella

Duties of the role/Responsibilities

• Collaboration with the CD process owners, responsible for leading and developing the learning strategy and training curriculum for CD processes and systems.
• Owns, designs and implements learning strategy for CD processes (e.g. Concept Sheet/Protocol and Amendments, Protocol Deviations, IB, CDP, Clinical Data Review, Medical Devices) and systems (e.g. protocol AI & authoring, protocol complexity, data review tools).
• Conducts needs analyses and assessments in collaboration with stakeholders to develop the role specific learning strategy for CD processes and systems.
• Partners with the CD Process Owner and other CD stakeholder to provide effective learning strategy for CD processes and systems.
• Closely collaborates with the Clinical Development Capability and Engagement team and the GCO Process, Training and GCP Compliance team in case of cross-functional processes and systems.
• Develops and deploys learning interventions in alignment with the overall learning strategy, integrating latest innovative learning methods and technology.
• Participates in and/or leads multidisciplinary teams to support continuous process learning improvement
• Facilitates and works on mechanisms for best practice sharing and continuous improvement efforts.
• Accountable for learning effectiveness measures and continuous improvement of learning effectiveness for CD processes and systems.

Education/Experience

• 7+ years’ working experience in (i.e. planning/executing/managing and/or monitoring clinical trials).
• Profound understanding of drug development process, including expert knowledge of international standards (GCP/ICH), health authorities (e.g. FDA/EMEA), and GCP-standards.
• Excellent project management capabilities with demonstrated ability to problem solve, manage stakeholders and work effectively in a matrix environment.
• Significant experience as training manager, facilitator and/or course curriculum developer with proven experience in LMS management, instructional design and adult learning.
• Strong facilitation skills, cross-functional and cross-cultural communication skills, stakeholder engagement and ability to lead without formal authority.
• Excellent interpersonal and communication skills
• Needs to be able to work independently

Interested candidates should submit an updated CV.

Please click the link below to apply, alternatively send an up to date CV to anett@peglobal.co.uk

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***