Director of Scientific Publications Job at Life Science Talent (San Francisco Bay Area)

Senior Director Public Health

The Senior Director, Public Health provides scientific and strategic leadership ...

Location

United States , Washington, DC

Salary:

150000.00 - 165000.00 USD / Year

American Cleaning Institute

Expiration Date

Until further notice

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

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

Director of Scientific Publications

The Director of Scientific Publications operates at the intersection of medical ...

Location

United States , New York

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

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

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

Director of Scientific Publications

The Director of Scientific Publications operates at the intersection of medical ...

Location

United States , Massachusetts

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

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

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

Senior Manager, Evidence Generation Lead

The medical Director, evidence generation is responsible for supporting strategi...

Location

Belgium , Mechelen

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

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

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

We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development

Medical Director, Global Evidence Generation Lead

The medical Director, evidence generation is responsible for supporting strategi...

Location

Belgium , Mechelen

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

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

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

We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development

Director, Medical Affairs - Osteoporosis

As an Associate Director / Director, Global Medical Affairs at Theramex, you wil...

Location

United Kingdom , London

Salary:

Not provided

Theramex

Expiration Date

Until further notice

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

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

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

Nephrology Transplant Physician Scientist

Hackensack Meridian Health is seeking a Nephrology Transplant Physician Scientis...

Location

United States , Hackensack

Salary:

198930.00 USD / Year

American Society of Transplantation

Expiration Date

Until further notice

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

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

health, dental, vision, paid leave, tuition reimbursement, and retirement benefits

New

Senior Director, Respiratory Innovation, VID Global Epidemiology & RWE

The Senior Director, Respiratory Innovation, Vaccines and Infectious Disease, Gl...

Location

United States; Belgium; United Kingdom; Netherlands , Collegeville, Pennsylvania; Amsterdam, Netherlands; Wavre, Belgium; Rockville, Maryland; London, United Kingdom

Salary:

224400.00 - 374000.00 USD / Year

GSK

Expiration Date

Until further notice

Requirements

PhD, DrPH, MD, or other doctoral degree in epidemiology, public health, biostatistics, or a closely related quantitative discipline
At least 8 years of experience conducting pharmacoepidemiology or real-world evidence (RWE) studies
Experience designing and conducting observational studies (e.g., post-approval studies, real-world evidence generation)
Experience leading epidemiology programs supporting clinical development and/or regulatory decision-making
Experience within the pharmaceutical, biotechnology, vaccine, or related research environment
Experience building and managing or leading teams of scientific or technical professionals
Experience authoring or contributing to scientific publications or regulatory documents

Job Responsibility

Provide strategic leadership in epidemiology and real-world evidence across multiple programs and assets
Lead and develop a team of epidemiologists, ensuring high-quality scientific output and delivery
Oversee the design and execution of epidemiologic studies, including observational and post-approval studies
Partner with cross-functional teams (e.g., clinical sciences, safety, regulatory) to support research and development programs and evidence generation
Contribute to governance and strategic decisions at an above-asset level
Oversee scientific dissemination, including publications, conference presentations, and regulatory documents
Build and maintain external collaborations with academic institutions, consortia, and research organizations

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes
Health care and other insurance benefits (for employee and family)
Retirement benefits
Paid holidays, vacation
Paid caregiver/parental and medical leave

Fulltime

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Director of Scientific Publications

Job Description

Job Responsibility

Requirements

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Director of Scientific Publications

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