CrawlJobs Logo

Director of Scientific Publications

life-science-talent-solutions.dk Logo

Life Science Talent

Location Icon

Location:
United States , New York

Category Icon
Category:
IT - Administration

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided
Save Job
Save Icon
Apply Position

Job Description:

The Director of Scientific Publications operates at the intersection of medical strategy and publication execution, partnering directly with Medical Directors and Scientists at Hemab Therapeutics. This role requires both strategic thinking to assemble evidence generation plans and hands-on expertise to author manuscripts, develop scientific platforms, and manage publication timelines. We do it because we believe when clinicians see better evidence, they change practice—and when practice changes, patients with rare diseases finally get the care they deserve. We are a small team of drug developers advancing novel therapies with elegant science. It's intellectually demanding, it's mission-driven, and if you think you're a good fit we'd love to hear from you.

Job Responsibility:

  • Partner with Medical Directors to translate medical strategies into comprehensive evidence generation plans, identifying high-impact publication opportunities aligned with clinical development milestones and launch objectives
  • Develop and maintain scientific platforms to support evidence generation plans, ensuring consistent disease and product narratives across all publication outputs
  • Lead end-to-end publication execution: author manuscripts and abstracts, develop congress materials, manage timelines from outline to submission, coordinate internal and external review cycles, assess resource needs for each project, implement SOPs and quality standards, and ensure submission excellence across all deliverables
  • Operationally support publication steering committees, identifying evidence gaps, cross-functional alignment, and timely delivery of tactical plan
  • Integrate patient voice through lived experience expert co-authorship and novel publication approaches to elevate patient voice
  • Oversee Medical Communications/Publications agency partnerships, including scope, deliverables, timelines, and budget

Requirements:

  • 5+ years of experience in pharmaceutical/biotech medical affairs, scientific publications, and/or HEOR
  • Track record of successful evidence plan delivery from concept through publication in peer-reviewed journals and conferences
  • Expert knowledge of GPP, ICMJE, and applicable publications guidelines and industry standards
  • Strong scientific writing and editing across publication types (clinical trial manuscripts, real-world evidence, reviews, congress abstracts)
  • Experience using publications management software
  • Understanding of medical communications strategies and omnichannel dissemination approaches
  • Proven project management skills with ability to manage multiple concurrent publications
  • Clinical trial literacy and ability to translate complex data into compelling narratives

Nice to have:

  • Experience at high-growth biotechnology companies across multiple product launches
  • Portfolio demonstrating creative publication outputs (visual abstracts, infographics, patient-led publications)
  • Therapeutic expertise in bleeding disorders
  • Experience with HEOR and real-world evidence publications
  • Fast adopter of technology and artificial intelligence

Additional Information:

Job Posted:
May 03, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Icon
Life Science Talent - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon
PREMIUM
More languages and countries
+ Unlock 31694 hidden job offers
Languages
English Čeština Deutsch Ελληνικά Español Français +15
Countries
United States United Kingdom India Canada Australia +
See plans
Plans from $2.99 / month

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Director of Scientific Publications

Senior Director Public Health

The Senior Director, Public Health provides scientific and strategic leadership ...
Location
Location
United States , Washington, DC
Salary
Salary:
150000.00 - 165000.00 USD / Year
cleaninginstitute.org Logo
American Cleaning Institute
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree required or Doctorate preferred, in public health, or a related field
  • Minimum 5 years of experience in scientific research management, regulatory science, or related public health programs
  • experience with FDA-regulated products strongly preferred
  • Demonstrated experience managing multi-stakeholder research programs or clinical studies under FDA frameworks
  • Comprehensive understanding of FDA rules and regulations, topical antiseptic safety and efficacy requirements, and relevant regulatory guidance
  • Excellent scientific writing and communication skills, including experience preparing manuscripts, white papers, and regulatory submissions
  • Exceptional oral and written communication skills
  • Ability to interact productively with both internal and external stakeholders, including non-scientific audiences
  • Proven ability to manage contractors, academic partners, and collaborations on scientific projects
  • Ability to work within a team environment as well as independently
Job Responsibility
Job Responsibility
  • Lead and oversee ACI’s Topical Antiseptics Program, including clinical and technical research supporting the FDA OTC Monographs and related scientific priorities
  • Keep abreast of emerging science and regulatory policies, monitor technical literature, and write and review technical reports, white papers, and publications for peer-reviewed scientific journals
  • Direct design, execution, and analysis of studies assessing product safety, efficacy, and antimicrobial benefits. Ensure compliance with regulatory and scientific standards
  • Serve as the primary scientific liaison to FDA and other regulatory bodies on antiseptic-related topics
  • interpret and communicate evolving regulatory expectations to ACI leadership and members
  • Coordinate and facilitate scientific work groups, technical committees, and member coalitions advancing antiseptic science
  • Prepare status/progress reports for presentation to ACI’s leadership and members
  • Develop and administer program budgets and deliverables
  • oversee contracts, research partnerships and consultant engagement
  • Develop and deliver scientific messaging for external stakeholders such as at scientific and technical conferences and meetings, and audiences for ACI technical communications
Read More
Arrow Right

Director of Scientific Publications

The Director of Scientific Publications operates at the intersection of medical ...
Location
Location
United States , Massachusetts
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 5+ years of experience in pharmaceutical/biotech medical affairs, scientific publications, and/or HEOR
  • Track record of successful evidence plan delivery from concept through publication in peer-reviewed journals and conferences
  • Expert knowledge of GPP, ICMJE, and applicable publications guidelines and industry standards
  • Strong scientific writing and editing across publication types (clinical trial manuscripts, real-world evidence, reviews, congress abstracts)
  • Experience using publications management software
  • Understanding of medical communications strategies and omnichannel dissemination approaches
  • Proven project management skills with ability to manage multiple concurrent publications
  • Clinical trial literacy and ability to translate complex data into compelling narratives
Job Responsibility
Job Responsibility
  • Partner with Medical Directors to translate medical strategies into comprehensive evidence generation plans, identifying high-impact publication opportunities aligned with clinical development milestones and launch objectives
  • Develop and maintain scientific platforms to support evidence generation plans, ensuring consistent disease and product narratives across all publication outputs
  • Lead end-to-end publication execution: author manuscripts and abstracts, develop congress materials, manage timelines from outline to submission, coordinate internal and external review cycles, assess resource needs for each project, implement SOPs and quality standards, and ensure submission excellence across all deliverables
  • Operationally support publication steering committees, identifying evidence gaps, cross-functional alignment, and timely delivery of tactical plan
  • Integrate patient voice through lived experience expert co-authorship and novel publication approaches to elevate patient voice
  • Oversee Medical Communications/Publications agency partnerships, including scope, deliverables, timelines, and budget
  • Fulltime
Read More
Arrow Right

Director of Scientific Publications

The Director of Scientific Publications operates at the intersection of medical ...
Location
Location
United States , San Francisco Bay Area
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 5+ years of experience in pharmaceutical/biotech medical affairs, scientific publications, and/or HEOR
  • Track record of successful evidence plan delivery from concept through publication in peer-reviewed journals and conferences
Job Responsibility
Job Responsibility
  • Partner with Medical Directors to translate medical strategies into comprehensive evidence generation plans, identifying high-impact publication opportunities aligned with clinical development milestones and launch objectives
  • Develop and maintain scientific platforms to support evidence generation plans, ensuring consistent disease and product narratives across all publication outputs
  • Lead end-to-end publication execution: author manuscripts and abstracts, develop congress materials, manage timelines from outline to submission, coordinate internal and external review cycles, assess resource needs for each project, implement SOPs and quality standards, and ensure submission excellence across all deliverables
  • Operationally support publication steering committees, identifying evidence gaps, cross-functional alignment, and timely delivery of tactical plan
  • Integrate patient voice through lived experience expert co-authorship and novel publication approaches to elevate patient voice
  • Oversee Medical Communications/Publications agency partnerships, including scope, deliverables, timelines, and budget
  • Fulltime
Read More
Arrow Right

Senior Manager, Evidence Generation Lead

The medical Director, evidence generation is responsible for supporting strategi...
Location
Location
Belgium , Mechelen
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 7+ years of experience in evidence generation, clinical development, HEOR, or a related field, with at least 5 years of experience in Epidemiology, Health Economics Outcomes Research (HEOR), or/and Health Systems Research
  • Proven track record of developing and implementing integrated evidence generation plans in the pharmaceutical or biotechnology industry
  • Experience in design, conduct and oversight of real-world evidence studies ranging from protocol writing to project management oversight and data interpretation and communication
  • Solid understanding of the cross functional drug development lifecycle and processes (Business Development, clinical trial design, conduct, & endpoint selection, Clinical Operations, Data Management, Biostatistics, and Regulatory)
  • Demonstrated expertise and experience working with methods for evidence generation using primary and secondary data sources, knowledge of common issues and challenges of implementation, and track-record of successful publications
  • Demonstrated depth of understanding of observational research methods, regulatory standards, and ability to leverage epidemiologic and data science expertise to meet evolving business needs
  • Evidence of technical expertise of applying pharmacoepidemiology evidence and insights at the therapy/product level
  • Ability to explain strengths and limitations of clinical practice datasets — such as electronic health records, claims, clinical data registries, patient generated health data, and other health data sources — in context of designing pharmacoepidemiology study designs
  • Ability to work successfully in a matrix and quick paced environment
  • Ability to multitask priorities to align with program objectives
Job Responsibility
Job Responsibility
  • Collaborate with cross-functional colleagues to Lead the development and execution of Medical evidence generation strategy and tactics supporting products in development as well as those commercially available, with appropriate prioritization and use of resources ensuring alignment with corporate goals, regional needs, and therapeutic priorities
  • Oversee the Design and implementation of Integrated Evidence Generation Plans (IEGPs) that incorporate clinical, real-world, and economic data to support product positioning and value demonstration
  • Scope RWE studies (Regional/National/Academic/Patient/Vendor), selection of new or existing academic (can include: ISR/lIS/NIS)/non-governmental registries (retrospective/prospective), management across various phases from start up, maintenance to final deliverables
  • Translate (early) trial efficacy to real-world comparative effectiveness as part of early and late phase study planning, identification of subpopulations, and for potential risk-sharing purposes
  • Design and implement multiple database and/or de novo (e.g. registries) pharmacoepidemiologic studies, as well as literature reviews, intended to provide insight into background epidemiology, disease state regular care, and/or quantify benefits and/or risks potentially associated with Alfasigma products
  • Project management oversight – ensuring effective design, initiation and implementation of real world evidence studies, while ensuring effective study protocols and plans, managing budget and milestone tracking, and where appropriate contracting with partner organizations
  • keep abreast on new data and developments in the field, key publications of interest, research methodologies and regulatory standards across the EU and New Markets regions and proactively address HOR strategy changes in collaboration with global and regional teams in anticipation of any trends
  • Review and provide relevant RWE/HOR inputs to statistical analysis plans and analysis outputs
  • Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team
  • Establish metrics to evaluate the effectiveness and impact of evidence generation activities on corporate and product-specific objectives
What we offer
What we offer
  • We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development
Read More
Arrow Right

Medical Director, Global Evidence Generation Lead

The medical Director, evidence generation is responsible for supporting strategi...
Location
Location
Belgium , Mechelen
Salary
Salary:
Not provided
it.alfasigma.com Logo
Alfasigma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 7+ years of experience in evidence generation, clinical development, HEOR, or a related field
  • At least 5 years of experience in Epidemiology, Health Economics Outcomes Research (HEOR), or/and Health Systems Research
  • Proven track record of developing and implementing integrated evidence generation plans in the pharmaceutical or biotechnology industry
  • Experience in design, conduct and oversight of real-world evidence studies ranging from protocol writing to project management oversight and data interpretation and communication
  • Solid understanding of the cross functional drug development lifecycle and processes (Business Development, clinical trial design, conduct, & endpoint selection, Clinical Operations, Data Management, Biostatistics, and Regulatory)
  • Demonstrated expertise and experience working with methods for evidence generation using primary and secondary data sources, knowledge of common issues and challenges of implementation, and track-record of successful publications
  • Demonstrated depth of understanding of observational research methods, regulatory standards, and ability to leverage epidemiologic and data science expertise to meet evolving business needs
  • Evidence of technical expertise of applying pharmacoepidemiology evidence and insights at the therapy/product level
  • Ability to explain strengths and limitations of clinical practice datasets — such as electronic health records, claims, clinical data registries, patient generated health data, and other health data sources — in context of designing pharmacoepidemiology study designs
  • Ability to work successfully in a matrix and quick paced environment
Job Responsibility
Job Responsibility
  • Collaborate with cross-functional colleagues to Lead the development and execution of Medical evidence generation strategy and tactics supporting products in development as well as those commercially available, with appropriate prioritization and use of resources ensuring alignment with corporate goals, regional needs, and therapeutic priorities
  • Oversee the Design and implementation of Integrated Evidence Generation Plans (IEGPs) that incorporate clinical, real-world, and economic data to support product positioning and value demonstration
  • Scope RWE studies (Regional/National/Academic/Patient/Vendor), selection of new or existing academic (can include: ISR/lIS/NIS)/non-governmental registries (retrospective/prospective), management across various phases from start up, maintenance to final deliverables
  • Translate (early) trial efficacy to real-world comparative effectiveness as part of early and late phase study planning, identification of subpopulations, and for potential risk-sharing purposes
  • Design and implement multiple database and/or de novo (e.g. registries) pharmacoepidemiologic studies, as well as literature reviews, intended to provide insight into background epidemiology, disease state regular care, and/or quantify benefits and/or risks potentially associated with Alfasigma products
  • Project management oversight – ensuring effective design, initiation and implementation of real world evidence studies, while ensuring effective study protocols and plans, managing budget and milestone tracking, and where appropriate contracting with partner organizations
  • keep abreast on new data and developments in the field, key publications of interest, research methodologies and regulatory standards across the EU and New Markets regions and proactively address HOR strategy changes in collaboration with global and regional teams in anticipation of any trends
  • Review and provide relevant RWE/HOR inputs to statistical analysis plans and analysis outputs
  • Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team
  • Establish metrics to evaluate the effectiveness and impact of evidence generation activities on corporate and product-specific objectives
What we offer
What we offer
  • We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development
Read More
Arrow Right

Director, Medical Affairs - Osteoporosis

As an Associate Director / Director, Global Medical Affairs at Theramex, you wil...
Location
Location
United Kingdom , London
Salary
Salary:
Not provided
theramex.com Logo
Theramex
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Qualified medical professional (Degree in Human Medicine)
  • Proven Medical Affairs knowledge and expertise (ideally in women’s health or related)
  • Leadership experience—preferably at international scale
  • Solid experience in healthcare professional engagement
  • Outstanding communication and collaboration skills
  • Strong business acumen
  • Highest ethical standards with strong command of compliance and international health authority requirements
  • Final ABPI signatory status
  • Strategic, pragmatic, and agile—thriving in fast‑paced, complex environments while delivering measurable outcomes
  • Passionate about women’s health and motivated to create tangible impact through science and education
Job Responsibility
Job Responsibility
  • Own and develop the global medical strategy for a portfolio of pharmaceutical products within the therapeutic area
  • Design and implement Medical Operating Plans in close collaboration with brand/product directors and other cross‑functional teams
  • Plan and supervise evidence generation projects (e.g., real‑world evidence)
  • Review and approve investigator‑initiated studies
  • Lead scientific publications, presentations, and dissemination of medical‑scientific data both internally and externally
  • Establish and maintain relationships with Global key medical experts, Healthcare providers, Academic institutions, Government agencies, Medical‑scientific societies, Advocacy groups
  • Create and implement engagement plans for medical‑scientific experts and patient advocacy groups
  • Lead advisory boards and other strategic scientific forums
  • Act as a senior medical‑scientific consultant to internal stakeholders, including Commercial brand teams, Regulatory Affairs, Market Access, Business Development, Other internal partners
  • Facilitate alignment across functions to ensure medical‑scientific integrity
What we offer
What we offer
  • A fast‑paced environment with broad exposure, where you can grow—even beyond your area of expertise
  • A culture that supports continuous learning, celebrates success, and recognises high performance
  • Opportunities for driven, talented professionals who want to be part of our ambitious, purpose‑led journey
Read More
Arrow Right

Nephrology Transplant Physician Scientist

Hackensack Meridian Health is seeking a Nephrology Transplant Physician Scientis...
Location
Location
United States , Hackensack
Salary
Salary:
198930.00 USD / Year
myast.org Logo
American Society of Transplantation
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • MD or equivalent foreign degree
  • Completion of an Internal Medicine Residency and Transplant Fellowship
  • Consideration for applicants with strong transplant experience during/after a Nephrology Fellowship
  • Minimum 3 years in a funded research program
  • Demonstrated success securing NIH and/or foundation funding
  • Peer-review experience (manuscripts, grants, editorial boards, or review committees)
  • Minimum of 15 scientific publications, with majority as first or last author
  • Board Certified in Internal Medicine
  • Board Certified or Board Eligible in Nephrology
  • Eligible for New Jersey Medical License
Job Responsibility
Job Responsibility
  • Conduct impactful basic or translational research in transplant/immunology
  • Pursue grant funding and philanthropic support to sustain laboratory operations
  • Lead and oversee laboratory processes, research staff, budgeting, and financial management
  • Establish strategic research goals aligned with the clinical goals of the Division of Organ Transplantation
  • Hold regular oversight meetings with the Chief Scientific Officer and Director of Transplantation
  • Develop and implement laboratory policies, procedures, and personnel decisions
  • Mentor and evaluate lab staff performance
  • Participate in professional activities, including consulting, editorial work, training, study sections, seminars, and national/international conferences
  • Evaluate potential living donor and transplant recipient candidates
  • Provide inpatient and outpatient care for pre- and post-transplant donors and recipients
What we offer
What we offer
  • health, dental, vision, paid leave, tuition reimbursement, and retirement benefits
Read More
Arrow Right

Senior Director, Seasonal Vaccines

You will help set scientific strategy for a seasonal viral vaccine program based...
Location
Location
United States , Pearl River
Salary
Salary:
214900.00 - 341100.00 USD / Year
pfizer.de Logo
Pfizer
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD in Virology or a related field
  • 10+ years industry or biotech experience in pre-clinical research and in vaccine technical development, with basic scientific expertise in SARS-CoV-2 research, immunology, serology, RNA vaccine technologies, and synthetic virology
  • Practical knowledge of global SAR-CoV-2 surveillance, recommendation, and regulatory systems
  • Experience providing scientific leadership for projects in the pharmaceutical industry, and proven track record of project advancement and delivery in vaccines
  • Global scientific reputation as evidenced by publication record and interaction with NIH or other established government research agencies
  • Understanding the scientific and non-scientific aspects of vaccines, and viral vaccine scientific, clinical and competitive landscape
  • Demonstrated innovation and experience to applying knowledge, techniques and skills to identify and validate best new technologies
  • Strong communication skills including public speaking experience and scientific writing
  • Experience collaborating cross functionally
  • Scientific analysis experience
Job Responsibility
Job Responsibility
  • Support and enhance the current infrastructure and processes required to enable robust and rapid development and licensure of variant-adapted COVID-19 vaccines
  • Represent Research on the cross-functional Vaccine Product Team, operating at the interface between research and development and coordinating with non-research functions to meet program goals, including life cycle management
  • Establish relationships with and serve as a primary scientific liaison with external alliance partners, including collaborating companies, government agencies and non-governmental organizations
  • Actively manage project risks, devising and implementing appropriate mitigation activities with multidisciplinary teams
  • Lead timely and effective communication of project risks and impact to senior leaders
  • Ensures that intellectual property is appropriately obtained and safeguarded
  • Take a key role in communication about vaccine programs in internal Pfizer documents and external patent applications, regulatory submissions, scientific papers, and conferences
  • Leads a motivated, committed and engaged research team to provide preclinical data to support annual strain change activities as well as exploration of next-generation vaccine technologies, leading direct reports and non-reports, reviewing experimental designs and data
What we offer
What we offer
  • eligibility for participation in Pfizer’s Global Performance Plan with a bonus target of 22.5% of the base salary
  • eligibility to participate in our share based long term incentive program
  • 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
  • paid vacation, holiday and personal days
  • paid caregiver/parental and medical leave
  • health benefits to include medical, prescription drug, dental and vision coverage
  • Relocation Support Available
  • Fulltime
Read More
Arrow Right