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About the Role

Autolus is passionate about pushing the boundaries of cancer therapy and autoimmune disease to deliver life-changing treatments to patients. We offer a flexible, diverse, and dynamic working environment that promotes creativity, leadership, and teamwork.

Responsibilities

Map cross-functional market needs across global regions to formulate the master Scientific Communication Platform (SCP).
Ensure pull-through of the SCP across all medical content and commercial asset strategies.
Manage the global matrix organization to drive quality planning and timely delivery of medical communications plans and scientific narratives.
Develop and execute global publication plans to support product lifecycle objectives and address data gaps.
Communicate product differentiation to HCPs, payers, and patients.
Align publication plans with clinical trial readouts, market access priorities, and asset commercialization milestones.
Adjust communications plans based on clinical trial results, healthcare landscape changes, and brand strategy.
Lead high-quality journal submissions, publications, congress presentations, and scientific medical content delivery.
Prioritize tactics within budget targets and allocated resources.
Serve as a subject matter expert on the scientific communication landscape, HCP preferences, and data dissemination.
Represent Autolus scientific communications to external investigators, key authors, and journal editors.
Establish strong collaborations with internal and external disease-area experts.
Ensure quality data analysis and interpretation, market-level communication planning, and data disclosure.
Ensure clear, accurate, scientifically rigorous, and timely communication of scientific data.
Promote and reinforce publication principles among authors and internal stakeholders.
Ensure publications are authored, written, and reviewed according to best practices and industry standards.
Evaluate and interpret medical literature and write market-level medical information.
Provide guidance on escalated medical information enquiries.
Demonstrate understanding of legal, regulatory, and compliance frameworks for pharmacovigilance issues.
Communicate trends and contribute to the identification and resolution of unmet medical need.
Serve as the point of contact between Scientific Communications and other matrix partners.
Share scientific communications plans to ensure awareness and connectivity.
Ensure endorsement of scientific communications plans by relevant governance bodies.
Conduct medical surveillance of enquiries and contribute to the identification and resolution of unmet medical need.
Contribute to Medical Information processes for responding to unsolicited enquiries.
Partner with market Medical colleagues to assess, plan, and allocate resources, including budget and biostatistical services.
Partner externally with third-party vendors for work execution.
Liaise with alliance and collaboration partners as required.
Enable and assist the Medical Communications team with the collection and collation of market-specific metrics.
Function as a high-performing partner, emphasizing teamwork, cooperation, accountability, and quality.

Requirements

Three or more years of pharmaceutical industry experience with a focus on scientific publications or medical communications.
Strong knowledge and experience with Good Publication Practice (GPP).
Strong scientific knowledge of therapeutic and disease research areas and familiarity with drug development and product lifecycle.
Experience leading medical communications across all phases of drug development and commercialization.
Ability to analyze and interpret complex clinical trial, real-world, and health economic and outcomes data.
Experience in leadership roles, including line management and people development.
Demonstrated track record of leading and executing in a highly matrixed environment across multiple functional areas, global geographies, and markets.
Ability to manage multiple, complex, and competing priorities and deliver quality work.
Ability to influence and negotiate appropriate solutions and establish strong stakeholder relationships.
Ability to participate flexibly in teleconferences and virtual meetings across different time zones.
Ability to travel domestically and internationally.
Knowledge of external compliance, transparency, and conflict-of-interest regulated work environments.
Knowledge of Good Publication Practices and guidance, including GPP and ICMJE, the Sunshine Act, Pharma Code of Conduct, and other guidance relating to post-marketing practices and scientific data communication.
Knowledge of medical information and medical communication, including the applicable legal, regulatory, and compliance framework.
Understanding of clinical trial design and execution, statistical methods, and clinical trial data reporting requirements.
Knowledge of management information systems, databases, and digital application of information.
Knowledge of the Microsoft suite of applications.

Skills

Scientific Communication Platform (SCP) formulation
Medical content strategy
Commercial asset strategy
Publication planning and execution
Scientific leadership
Data dissemination
Subject matter expertise
Stakeholder engagement
Budget management
Resource allocation
Vendor management
Good Publication Practice (GPP)
Medical Information
Health Economics and Outcomes Research (HEOR)
Clinical trial design and execution
Statistical methods
Data analysis and interpretation
Leadership
Organizational skills
Communication skills (written and verbal)
Interpersonal skills
Time management skills
Negotiation skills
Teamwork
Cooperation
Accountability
Quality commitment

Location

Work Type

Flexible
Full-time

Experience Level

Three or more years of pharmaceutical industry experience
Experience in leadership roles
Experience leading medical communications

Education Level

Advanced scientific degree (e.g., PharmD or PhD)
Certified Medical Publication Professional (CMPP) desired

About the Company

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 is committed to providing an inclusive and fair workplace for all.
Autolus’ success is driven by equality and inclusion; we believe all voices are of equal value and must be heard.
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 where appropriate.
We also provide reasonable accommodations throughout the recruitment process.