Director, Scientific Publications
2 weeks ago
**The Position**
The Publications Director will deliver on all aspects of biomedical publications development, with mínimal supervision.
**Responsibilities**
- Lead end-to-end publications development aligned to therapeutic area strategy across the portfolio and pipeline
- Execute the development of value
- and impact-driven publications (abstracts, posters/orals, primary and secondary manuscripts, review articles).
- Contribute to strategic publication planning activities and tactics via active participation in relevant subcommittees.
- Vendor oversight and KPI assessments.
**Tasks**:
- Develop publication content (abstracts, posters, orals/slides, primary and secondary manuscripts, review articles, enhanced content/publication extenders) for high-complexity and/or high priority projects.
- Review publication content developed by vendors/junior staff, providing constructive feedback; ensure execution of tactics/monitor timelines.
- Participate in publication planning meetings/subcommittees for assigned products/therapy areas, and advise on strategy and tactics.
- Lead publication kickoff meetings with internal and external stakeholders to achieve strategic and scientific alignment.
- Train cross-functional colleagues on the publication process and ensure publications are developed per SOP.
Competencies:
- Understands the current publications landscape and applies this expertise to develop strategic, value-driven publications for small-molecule, biologic, and device assets from pipeline to market.
- Ability to prioritize to deliver on multiple ongoing projects with the appropriate sense of urgency and sound judgement for issue resolution/escalation.
**Required Education, Experience and Skills**
- A health, life science, or medical science degree (Masters, Doctorate, PharmD, or MD) and fluent in English (written and spoken).
- Professional certification, preferred.
- International Society for Medical Publication Professionals Certified Medical Publication Professional (ISMPP CMPP) credential.
- American Medical Writer’s Association (AMWA) Medical Writer Certified (MWC®) credential.
- Demonstrated competency in writing/editing/reviewing/managing complex publications for various audiences across the product lifecycle.
- Experience advising teams on target journal selection/congress identification and when to leverage enhanced digital content/publication extenders.
- Understands different study designs and evidence-generation platforms, e.g., RCTs, observational research, real-world evidence (RWE), claims databases, health economics & outcomes research (HEOR).
- Soft skills to manage internal/external author/stakeholder interactions independently.
- Experience writing in multiple TAs and aptitude to quickly learn new Therapeutic Areas (TAs).
- Proficiency with Microsoft Office (Word, Excel, PowerPoint) and publication management software (e.g., Datavision, Veeva Vault).
- Developing publications/strategic plans across the product lifecycle - pipeline to market access (small molecules/biologics/devices).
- Eight years relevant biopharmaceutical experience; experience in women’s health desired.
- Proficient in interpreting guidelines, influencing strategy, and managing author and vendor interactions.
**Who We Are**:
Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women’s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.
**US and PR Residents Only**
For more information about personal rights under Equal Employment Opportunity, visit:
EEOC Poster
EEOC GINA Supplement
OFCCP EEO Supplement
OFCCP Pay Transparency Rule
Organon proudly embraces diversity in all of its manifestations and is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity, or gender expression, national origin, disability, veteran status or any other characteristic protected by state or federal law.
**Search Firm Representatives Please Read Carefully**
**Applicable to United States Positions Only**:Under various U.S. state laws, Organon is required to provide a reasonable estimate of the salary range for this job. Final salary determinations take a number of factors into account including, but not limited to, primary work location, relevant skills, education level, and/or prior work experience. The applicable salary range for this position in the U.S. is stated below. Benefits offered in the U.S. include a retirement savings plan, paid vacation and holiday time, paid careg
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