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ASSOCIATE DIRECTOR (SCIENTIFIC PUBLICATIONS) - Gaithersburg Maryland
Company: AstraZeneca Location: Gaithersburg, Maryland
Posted On: 11/13/2024
Associate Director (Scientific Publications) Introduction to role: Join our Oncology R&D team as an Associate Director, Scientific Publications. In this role, you'll be responsible for the development of high-quality clinical publications and reviews for investigational pipeline products. You'll also collaborate with other team members to develop aspects of a Publication Plan under the supervision of the Publications Director. This is a unique opportunity to collaborate cross-functionally and ensure publication plans align with project strategy. Accountabilities: - Leads the publication development process to deliver high-quality publications, participating as a member of cross-functional teams, effectively collaborating with key partners, and ensuring compliance with internal and external publication guidelines.
- Collaborate cross-functionally to deliver publications plans that are aligned with project strategy.
- Accountable for managing 3rd-party providers in the delivery of defined publications activity, ensuring quality and delivery standards are adhered to.
- Develops and ensures that strategically aligned scientific communication points are delivered and that statements and conclusions in publications are accurate and supported by appropriate data.
- Provide on-site support at key scientific congresses and meetings.
- Ensures the high quality and clarity of publications by maintaining/promoting familiarity with ICMJE, GPP3, CONSORT, AMA, and other external standards as well as AstraZeneca publication policies and procedures. Education & Experience Requirements: Education: PhD, PharmD, MD, or advanced scientific degree in a biomedical field Experience: 3+ years of experience in medical communications/publications in pharmaceutical/biotech industry, medical communications agency, CRO, publishing or academic setting with equivalent work experience Essential Skills & Experience:
- Demonstrated project management, organization, and time management skills
- Knowledge and understanding of GPP3, ICMJE, AMA, and other publication standards
- Knowledge and understanding of publication strategy and planning
- Previous experience with management of contract resources/vendors
- Ability to analyze critically and synthesize scientific information from a broad range of scientific disciplines and clinical therapeutic areas
- Strong communication and leadership skills; ability to work collaboratively with diverse teams Desired Qualifications:
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