job summary: We are seeking a REMOTE Senior Manager, Global Medical Affairs Resource, to work with a leading biopharmaceutical company based out of Thousand Oaks, CA. This is a great opportunity to make a global impact! You with be responsible for creating and maintaining Medical Affairs slide decks. The Medical Writer will collaborate with Medical Affairs stakeholders to create high-quality, evidence-based medical content for use in internal training, external scientific exchange and digital platforms. This is a remote-based role with no direct reports. location: Telecommute job type: Contract salary: $72.28 - 85.03 per hour work hours: 9 to 5 education: Masters responsibilities: Under the leadership of the Associate Director, Global Resource Lead, collaborate cross-functionally to develop scientific resources, including scientific/clinical slide decks, field resources and digital content for external use by Global Medical Affairs. Liaise with Global Publication Planning Leads and monitor the medical literature and conference abstracts for new reports in the therapeutic area for inclusion in Medical Affairs resourcesIncorporate insights into medical resource development and ensure alignment with Medical strategyConduct literature searches and analyze results to identify scientifically robust supporting references for Medical Affairs resourcesCoordinate resource development with internal subject matter expertsWork with Medical Affairs colleagues to develop project timelines and ensure on-time delivery of resources; effectively communicate project timelines and project status to stakeholdersAnticipate and mitigate risks to on-time deliveryDevelop and maintain slide deck templates, including layouts, formats, colors, and style guides, working with or managing vendors as neededEvaluate and interpret medical insights, medical strategy, and stakeholder expertise to identify, develop, and update materials appropriatelyMedical/scientific content development to support omnichannel and digital initiativesCollaborate with Global Medical Affairs stakeholders to ensure global resources meet regional needs and develop local or country-specific resources as needed Ensure that key data statements and conclusions are consistent across related assetsManage all technical aspects of Medical Review Committee (MRC) reviews and approvals for new or updated Medical Affairs slide decks, including annotations, referencing, and comment adjudication, in collaboration with clinical subject matter experts and MRC members and administratorsContribute to annual content planning cycles and support the development of global training projects and initiativesAdhere to Company SOPs, work instructions, and quality standardsApply legal, regulatory, and compliance requirements to all Medical Affairs activities qualifications: MS degree or higher (PhD or Pharm.D) with 3-5 years' experience in pharmaceutical or agency medical affairs experience requiredMinimum of 3-5 years of experience creating scientific resources in a pharmaceutical, biotech, or agency/vendor setting for delivery to healthcare professionals and payorsComputer Skills Expert working knowledge of Microsoft Office SuiteExpertise in Adobe Creative Suite including Illustrator preferredExperience in Veeva strongly preferredFamiliarity with SharePoint and project management software preferred #LI-CV1 skills: Medical Publications, Veeva Vault Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.