FAQs
What is the primary responsibility of the Therapeutic Area Knowledge Transfer Director, Rare Diseases?
The primary responsibility is the design and delivery of all aspects of therapy area scientific training and knowledge assessment for a suite of rare disease products.
What qualifications are required for this position?
A relevant qualification ideally with a post-graduate degree e.g. MSc, PhD, MD, PharmD, or MBA, coupled with a proven track record in Medical Affairs or significant experience within a Medical Communications Agency working in Specialty Care.
Who does the Therapeutic Area Knowledge Transfer Director report to?
The Therapeutic Area Knowledge Transfer Director reports to the Head of Training and Capabilities.
Will I need to collaborate with other teams or departments?
Yes, you will collaborate with internal and external partners/providers, as well as cross-functional teams to assess therapeutic area and scientific knowledge.
Is experience in data analysis important for this role?
Yes, prior experience in data analysis and statistics for understanding clinical study results and in developing and delivering training is essential.
What types of training will I be responsible for overseeing?
You will oversee training related to clinical fluency and scientific expertise for all medical functions.
Will I be involved in identifying local training needs?
Yes, identifying local training needs, implementing solutions, and assessing outcomes will be part of your responsibilities.
How will I ensure that the training remains current?
You will ensure sustainability by developing training updates and revisions in a timely manner, in relation to new scientific updates.
What kind of work environment can I expect?
You can expect a dynamic and fast-moving organization that is focused on innovation and specialty care, with a strong emphasis on employee growth and development.
Is there an emphasis on compliance in this role?
Yes, compliance and collaboration are integral aspects of this role, ensuring all training aligns with company and regulatory standards.