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About the Role

The Executive Medical Director (EMD) will be responsible for building and directing the United Kingdom Medical Affairs (MA) strategy for a product or group of products, as well as developing and implementing the overall Medical Affairs strategy for dedicated Autolus products. The EMD will lead the implementation of the MA strategy including scientific communications, publications, congress planning, KOL engagement, advisory boards, and Investigator Initiated Trials (IIT) within the United Kingdom. The role focuses on optimizing patient access and outcomes by providing compound and disease area medical expertise, acting as a key expert in the relevant therapeutic area, and leading across functions to address stakeholder needs.

Responsibilities

Establish and lead the Medical Affairs for specific product(s) to provide strategic medical input to support pre-, peri- and post-launch activities.
Support commercial business plans, including product communications, and final signatory for all promotional materials and activities.
Develop and maintain the relevant KOL and other HCP relationships.
Develop a KOL/advisor network to leverage opportunities for the product portfolio.
Ensure regular contact as required with the UK and Ireland KOLs by the medical affairs team.
Leverage KOLs to support non promotional brand activities including market access, educational programs and publications.
Speaker decks for P2P meetings are reviewed and approved by the medical team in accordance with IPHA codes as appropriate.
Collaborate with market access steam to facilitate national and local reimbursement.
Ensure all employees in the UK and Ireland have the appropriate level of scientific knowledge.
Develop economic valuation and health outcomes research studies.
Develop and execute the medical communications plan in close coordination with Global medical affairs and the commercial organization.
Represent medical affairs at relevant UK, IRL and EU/Global Meetings and communicate outputs, engage with internal and external stakeholders.
Provide Quality Systems support for any activities which are connected to impact/investigation assessments for cell collection centres.
Establish scientific communication with KOLs and Scientific Health authorities.
Leading the development and management of Medical Affairs SOPs.
Development and implementation of country medical plan.
In collaboration with UK management team develop brand plans incorporating medical activities.
Maintain a high level of knowledge and appropriately implement current local pharmaceutical regulation, ensure implementation of Autolus policies and procedures, and enhance cross-functional understanding of compliance requirements.
Manage compliance of promotional materials with necessary regulations such as Blue Book, Human Medicines regulations 2012, PAGB code, IPHA Code and Statutory requirements and to provide input on compliance with the regulations to Medical and Marketing Departments.
Be the final Medical Signatory for materials, in compliance with the IPHA code and other regulations.
Be the point of contact for resolution of complex matters as needed.
Support and partner on training activities to Commercial, Clinical Research Associates (CRAs), Clinical Study Managers (CSMs), etc.
Support Drug Regulatory Affairs (DRA) team on regulatory documents, filing and health authorities’ interactions.

Requirements

Solid industry experience in medical affairs in hematology, cell therapy or oncology.
Breadth of experience in the biotechnology or pharmaceutical industry in United Kingdom.
Track record of working cross functionally on strategic planning, as well as creation of a Life Cycle Management plan.
Experience with full lifecycle development and medical support of successfully marketed biotechnology or pharmaceutical products.
Breadth of knowledge on ABPI Code and UK regulatory environment.

Skills

Expertise in establishing, coordinating, and chairing Advisory Boards with an established network of KOL in Oncology in England.
Working knowledge of regulatory and health economic requirements.
Focus on Results: Works to meet business goals set by management and leaders.
Builds Trust and Relationships: Ensures trust with internal and external partners by delivering on commitments.
Resilience: Has the capacity to recover quickly from difficulties; toughness.
Communicates and Collaborates: Builds partnerships and works collaboratively with others to meet objectives.

Location

London (hybrid)
United Kingdom

Work Type

Full Time
Hybrid

Experience Level

Estimated travel approx. 30%
Experience in the design real world evidence protocols and conduct of clinical trials in hematology/oncology a plus.
Disease expertise and knowledge of the treatment landscape for the disease area a plus.
Experience in hematology/oncology, gained through industry experience or with relevant specialty training in hematology or solid tumours (P).
Experience developing and/or launching a new pharmaceutical product/biologic product, CAR-T experience is preferred. (P).

Education Level

Degree in Bpharm or MD ( E)
The individual will ideally have appropriate professional certification in both medicine and pharmaceutical medicine (P).

Salary/Compensations

competitive salary
performance related bonus

Benefits

comprehensive benefits package

About the Company

Autolus is a biopharmaceutical company, advancing innovative therapies at both clinical and commercial stages of development, focused on next-generation, programmed T cell therapies for the treatment of cancer.
Using a broad suite of proprietary and modular T cell programming technologies, the company is engineering precisely targeted, controlled, and highly active T cell therapies designed to better recognize cancer cells, break down their defence mechanisms, and eliminate these cells.
Autolus has a pipeline of product candidates in development for the treatment of haematological malignancies, solid tumours, and autoimmune diseases.
Our team is passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and autoimmune diseases to deliver life-changing treatments to patients.
Whilst working at Autolus you will enjoy a flexible, diverse, and dynamic working environment which actively promotes creativity, leadership and teamwork.
Autolus is developing complex, breakthrough therapies for a globally diverse market and equally recognises that diversity amongst our people is critical to our mission.
As we draw on our differences, what we’ve experienced, and how we work, we celebrate diversity and are committed to creating an inclusive environment for all employees.
Autolus is committed to the protection of the personal information that we collect & process and we are fully compliant with General Data Protection Regulations (GDPR).
Autolus’ success is driven by equality and inclusion; we believe all voices are of equal value and must be heard.
Whilst operating with focus and integrity, we are committed to improving diversity and inclusion within our business and our industry.

Equal Opportunity

We are an equal opportunity employer and do not discriminate on the basis of race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected characteristic.
We also provide reasonable accommodations throughout the recruitment process.