Director, Global Publications Lead, Gastroenterology
The Director, Global Publications Lead, Gastroenterology, is a key strategic partner of the Gastroenterology and Immunology Medical Affairs teams, responsible for dynamically driving the strategic planning and tactical execution of the comprehensive publication plan. location: Cambridge, Massachusetts
job type: Contract
salary: $130 - 143 per hour
work hours: 9 to 5
education: Masters responsibilities:
In partnership with cross-functional stakeholders, the Global Publications Lead, Gastroenterology will:
- Own and lead the Scientific Publications Team meeting and annual workshops to drive the development of the strategic global publication plan for the assigned programs with the ability to lead and collaborate effectively across numerous and diverse internal and external stakeholders
- Provide and lead high level strategic thinking for innovative strategies in developing and disseminating the company's scientific and medical data at the Global level, including the integration of AI-enabled tools and digital platforms to enhance publication planning, data dissemination, and stakeholder engagement.
- Ensure and communicate regular updates to relevant key stakeholders to facilitate ongoing functional and regional planning and inform dependencies
- Collaborate with external authors and journals for the planning, integration, and execution of all publication activities
- Create a spirit of cooperation and collaboration and foster diversity of opinion and an environment of psychological safety and open communication in the establishment and execution of annual program strategies, objectives, tactics and priorities
- Bring deep subject matter expertise on innovative and compliant publication strategies, tactics and policies
- Ensure that all of the company's publication related activities are conducted according to company's standards, SOPs, applicable working instructions and, industry standards and educate on these policies as necessary
- Ensure high scientific quality, alignment with medical strategy and adherence to compliance/legal requirements
- Manage 3rd-party vendors to ensure delivery of quality publications on time and on budget
- Utilize and champion the use of AI and digital technologies to optimize publication workflows and processes, including applications in literature review, plain language summary creation, and innovative approaches to data synthesis and visualization
- Create, review and oversee the publication budget and serve as a financial steward in the creation of publication deliverable approaches and in the use of external vendors
- Ensure that vendors are properly trained to and comply with the company's standards, on SOPs, company systems and tools while managing all vendor partners to execute the tactical plan effectively and efficiently for their assigned publication projects
qualifications:
Qualifications
- A higher education degree (M.D., Pharm.D., Ph.D.), or master's degree in biomedical discipline or equivalent with demonstrated experience in publication management
- 8-10+ years of pharmaceutical industry experience, at least half of which is in Medical Affairs
- 5-8+ years' experience in medical publications/communications, or other related areas within the biopharmaceutical industry, preferably within a matrix structure, in Medical Affairs or Clinical Development (e.g. clinical scientist, medical information, medical communications, medical information, publications).
- CMPP certification preferred
- Prior experience in immune-mediated inflammatory diseases is preferred, especially in psoriasis or Gastroenterology
- Demonstrated experience in leveraging AI tools and/or digital technologies in scientific communications and publication planning.
- Understanding of the pharmaceutical drug development process, clinical trial design and execution, statistical methods, and clinical trial data reporting requirements.
- Deep knowledge of scientific publication planning processes and industry standards for reporting scientific studies including but not limited to GPP, ICMJE, COPE, CONSORT, STROBE, PRISMA
- Experience and knowledge of publication management software/systems
- Ability to foster diversity of opinion and an environment of open communication and trust
- Demonstrated ability in coordinating and implementing simultaneous projects within a complex global matrix and align region and country-specific priorities into a unified approach that meets multiple stakeholder needs
- Proactive, enterprise thinker with multicultural outlook, and the ability to work effectively in a geographically and functionally diverse organization.
- Experience in vendor and budget management
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 [email protected].
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.
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