In this role, you will be responsible for developing templates, graphics, and audio/visual materials for use in on-line training, interactive web-based, facilitator guides, PowerPoint presentations, participant guides and tests, job aids and other classroom materials.
Develop comprehensive provider specific plans to increase performance and improve outcomes for quality programs. Provide ongoing strategic recommendations, training and coaching providers and groups on program implementation and barrier resolution.
Contribute to design, execution and interpretation of preclinical safety, biocompatibility, analytical chemistry, and toxicological evaluation programs according to relevant regulatory requirements; including review of literature and assessment of compliance.
Ability to write reports, business correspondence, and policy/procedures. Ability to effectively communicate information, develop and deliver presentations in both verbal and written form across all levels of organization.