AstraZeneca
Director, Scientific Publications
AstraZeneca, Gaithersburg, Maryland, us, 20883
Are you ready to take the lead in the development of high-quality clinical publications and reviews for investigational pipeline products in Oncology R&D? As the Director, Scientific Publications, you will have the opportunity to develop and deliver strategic Publication Plans for pipeline assets, lead cross-functional publication teams, and ensure alignment with project and overall Oncology R&D strategy.
Responsibilities
In this role, you will be responsible for leading the cross-functional team in the publication development process, ensuring compliance with internal and external publication guidelines. You will lead 3rd-party providers in the delivery of defined publications activity, ensuring quality and delivery standards are adhered to. You will also provide on-site support at key scientific congresses and meetings, and mentor others during the flow of work.
Essential Skills/Experience:
PhD, PharmD, MD or advanced scientific degree in a biomedical field with proven scientific and/or publications expertise.
5+ years of demonstrated abilities in medical communications/publications in pharmaceutical/biotech industry, medical communications agency, CRO, publishing, or academic setting with equivalent work experience required.
Consistent record of collaborative and consultative cross-matrix abilities.
Ability to work within a large strategic framework, while maintaining strong attention to detail and compliance with global publication ethical standards and company publication policy and SOPs.
Working knowledge of publication strategy and planning.
Ability to understand and adhere to good publication practices and relevant guidelines on scientific data communication, such as ICMJE, GPP3, company policy and SOPs.
Experience leading contract resources/vendors.
Demonstrated ability and flexibility to prioritize while supporting multiple projects, dealing effectively with change and ambiguity.
Broad understanding of drug development process.
Demonstrated ability to establish and maintain professional relationships with external authorities, investigators, journal editors and publishers, and professional bodies.
Working knowledge of Datavision publication management systems, understanding of publication management databases (iEnvision, Datavision).
Demonstrated ability to mentor others during the flow of work.
Proficiency in Microsoft Office applications (Word, Excel, PowerPoint) required.
Desirable Skills
AMWA, BELS, and/or ISMPP (CMPP) certification.
Background in biologics and/or previous experience in oncology products.
Previous experience writing and editing peer-reviewed clinical publications highly desirable.
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Responsibilities
In this role, you will be responsible for leading the cross-functional team in the publication development process, ensuring compliance with internal and external publication guidelines. You will lead 3rd-party providers in the delivery of defined publications activity, ensuring quality and delivery standards are adhered to. You will also provide on-site support at key scientific congresses and meetings, and mentor others during the flow of work.
Essential Skills/Experience:
PhD, PharmD, MD or advanced scientific degree in a biomedical field with proven scientific and/or publications expertise.
5+ years of demonstrated abilities in medical communications/publications in pharmaceutical/biotech industry, medical communications agency, CRO, publishing, or academic setting with equivalent work experience required.
Consistent record of collaborative and consultative cross-matrix abilities.
Ability to work within a large strategic framework, while maintaining strong attention to detail and compliance with global publication ethical standards and company publication policy and SOPs.
Working knowledge of publication strategy and planning.
Ability to understand and adhere to good publication practices and relevant guidelines on scientific data communication, such as ICMJE, GPP3, company policy and SOPs.
Experience leading contract resources/vendors.
Demonstrated ability and flexibility to prioritize while supporting multiple projects, dealing effectively with change and ambiguity.
Broad understanding of drug development process.
Demonstrated ability to establish and maintain professional relationships with external authorities, investigators, journal editors and publishers, and professional bodies.
Working knowledge of Datavision publication management systems, understanding of publication management databases (iEnvision, Datavision).
Demonstrated ability to mentor others during the flow of work.
Proficiency in Microsoft Office applications (Word, Excel, PowerPoint) required.
Desirable Skills
AMWA, BELS, and/or ISMPP (CMPP) certification.
Background in biologics and/or previous experience in oncology products.
Previous experience writing and editing peer-reviewed clinical publications highly desirable.
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