CrawlJobs Logo

Scientific Content Lead

arena.ai Logo

Arena Intelligence, Inc.

Location Icon

Location:
United States , Bay Area

Category Icon
Category:
-

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided

Job Description:

Arena is seeking a Scientific Content Lead to define and defend the scientific credibility of the world’s most trusted AI evaluation platform. You’ll ensure that Arena’s methodology, data quality practices, and evaluation results are understood clearly by researchers, labs, policymakers, analysts, and enterprises. This role is deeply technical and highly cross-functional. You’ll work directly with our research team to translate evaluation science into rigorous public communication and content, anticipate methodological critiques, and uphold Arena’s commitment to transparency and neutrality.

Job Responsibility:

  • Own Arena’s scientific communications strategy, ensuring that our evaluation methodology, benchmarks, and data quality practices are clearly understood and accurately represented externally
  • Lead Arena’s proactive data quality narrative, defending against common critiques and mischaracterizations through transparency, evidence, and high-integrity storytelling
  • Develop canonical explanations of Arena’s measurement approach, including Bradley-Terry-Luce-style ranking, confidence intervals, and uncertainty-aware interpretation
  • Ensure that Arena’s leaderboards are communicated responsibly: rankings are statistical estimates, small differences are often noise, and uncertainty must be preserved in public interpretation
  • Anticipate, track, and respond to methodological critiques, especially around contamination, overfitting, gaming, distribution shift, and evaluation validity
  • Partner closely with researchers to translate technical work into rigorous public materials, including methodology documentation, research posts, and open-source releases
  • Support Arena’s Academic Partnerships Program, strengthening scientific connectivity through collaborations, citations, and peer-reviewed credibility
  • Create briefing materials for high-stakes audiences, including frontier AI labs, policymakers, analysts, and enterprise partners, ensuring that technical nuance survives external scrutiny
  • Serve as a scientific editor and reviewer across external communications, stress-testing claims before they become public narratives

Requirements:

  • 8-10 years of experience in AI/ML, evaluation, research, or scientific communications, with deep familiarity in how frontier model performance is measured and debated
  • Strong technical background in machine learning, benchmarking, or model evaluation, with the credibility to engage directly with leading labs and researchers
  • Exceptional writing and communication skills, especially the ability to explain complex methodology clearly without oversimplifying or overstating conclusions
  • Track record of producing scientifically rigorous external-facing work, such as technical publications, evaluation reports, methodology documentation, or research translation
  • Deep comfort operating in ambiguity, where uncertainty, tradeoffs, and limitations must be communicated transparently rather than smoothed over
  • High editorial judgment and the ability to identify where scientific nuance is most likely to be misunderstood or weaponized
  • Collaborative mindset and experience partnering across research, product, policy, and communications teams

Nice to have:

  • Direct experience working with large-scale human preference data, evaluation platforms, or benchmarking systems
  • Familiarity with common failure modes in AI evaluation, including contamination, overfitting, gaming, and distribution shift
  • Experience contributing to open source scientific tooling or methodology transparency efforts
  • Existing relationships within the AI research, safety, or evaluation community
  • Experience engaging with academic institutions, research alliances, or scientific journals
  • Comfort operating within neutrality and integrity constraints required of an independent evaluation platform
What we offer:
  • Comprehensive health and wellness benefits, including medical, dental, vision, and additional support programs
  • The opportunity to work on cutting-edge AI with a small, mission-driven team
  • A culture that values transparency, trust, and community impact

Additional Information:

Job Posted:
February 20, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
Job Link Share:
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 Scientific Content Lead

R&D Knowledge and Learning Manager (Content Development)

As a Senior Manager – TA/Product Knowledge & Learning (Content Development), you...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree with 10+ years of clinical/scientific affairs experience
  • Master's degree with 12+ years of experience
  • Bachelor's degree with 15+ years of experience
Job Responsibility
Job Responsibility
  • Partner with U.S.-based global Senior Managers within the Knowledge & Learning organization who serve as the product and Therapeutic Area learning leads
  • Develop high-quality, scientifically accurate, and engaging learning content that supports TA and product knowledge initiatives, including congress-related trainings
  • Act as a content execution and design partner, transforming strategic direction provided by U.S. Senior Managers into impactful learning assets
  • Support U.S. Senior Managers (Product/TA Learning Leads) by developing learning content aligned to product strategy and learning objectives
  • Work closely with the global K&L Sr Managers to create new learning materials while also refreshing and updating existing content to reflect new clinical data and scientific evidence, product strategy updates and insights and learnings from medical congresses
  • Design and develop a wide range of learning materials, including slide decks, facilitator guides, participant materials, infographics, visual summaries, quick-reference tools, and content to support congress-related trainings
  • Translate complex scientific, clinical, and product information into clear, concise, and visually engaging content
  • Apply adult learning principles and instructional design best practices
  • Incorporate interactive elements to support learning calls and virtual learning sessions
  • Manage content development timelines, version control, review cycles, and documentation
Read More
Arrow Right

Director, Global Content Design and Delivery, Oncology

The Director, Global Content Design and Delivery, Oncology in the Global Scienti...
Location
Location
United States; Switzerland; United Kingdom , Collegeville; Baar; Durham; London; Philadelphia; Upper Providence
Salary
Salary:
Not provided
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree in science, medicine, pharmacy, communications or a related field
  • 7+ years of related experience in scientific communications, medical content design and delivery, or a related field within the pharmaceutical or healthcare industry
  • Experience in leading cross-functional teams and driving strategic communication plans
  • Mastery developing and executing innovative communication tools, including digital and social media strategies
  • Project management expertise with multiple projects simultaneously, meeting deadlines
  • Experience in developing and delivering medical training materials
  • Proficiency in digital content creation and management tools with solid technical capabilities in Excel, PowerPoint, and Team sites
  • Interpreting, analyzing, organizing, and presenting complex data to a broad range of audiences required
Job Responsibility
Job Responsibility
  • Chair the Global Integrated Medical Communication Teams (GIMCT) for assigned assets/therapeutic areas to drive the development of Integrated Medical Communication Plans (IMCP), inclusive of content, channel, and congress plans/tactics
  • Drive key asset deliverables including the Scientific Communication Platform (SCP), Scientific Narratives, Content and Channel plans, Congress Plans and all associated tactics
  • Serve as a key partner to therapeutic area medical leaders, global publications, R&D, Global Medical Team (GMT), and priority markets and regions
  • Collaborate with internal stakeholders on the development and execution of innovative tools for internal and external communication, including digital/social medical delivery
  • Drive timely execution of all deliverables within the IMCPs for assigned assets, ensuring they are scientifically accurate, evidence-based, and comply with relevant regulations, industry guidelines, and ethical standards
  • Accountable for aligning with key stakeholders and for the input of the IMCP framework and related engagement planning elements within the asset annual business planning process
  • Lead annual scope of work development with procurement for IMCP deliverables with agencies of record, and provide continuous oversight and feedback to drive effective collaboration and partnership
  • Ensure content development follows all relevant codes and system requirements (e.g. ABPI code of practice, GSK Code, and use of Content Lab), particularly with respect to the delivery of promotional versus non-promotional information
  • Participate in initiatives on Gen AI platforms being leveraged for content creation and personalization/adaptation to ensure broader scalability and use
  • Gather and share best practices across Global to ensure consistency, high standards, and excellence are maintained across the organization
What we offer
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
  • Fulltime
Read More
Arrow Right

Scientific Medical Writer

We are seeking a Scientific Writer to serve as a critical bridge between our Res...
Location
Location
Denmark , Københavns Kommune
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD in life sciences, biomedical sciences, pharmacology, immunology, hematology, or related field
  • Demonstrated experience in scientific writing, including peer-reviewed publications as first author or significant contributor
  • Strong understanding of clinical drug development processes and regulatory requirements
  • Excellent written and verbal communication skills with the ability to translate complex scientific concepts for diverse audiences
  • Meticulous attention to detail and commitment to scientific accuracy
  • Strong organizational skills and ability to manage multiple projects simultaneously
  • Proven ability to work collaboratively in a fast-paced, team-oriented environment
Job Responsibility
Job Responsibility
  • Lead the preparation of scientific manuscripts for peer-reviewed publications, demonstrating our research and preclinical findings
  • Lead the preparation of patent filings
  • Develop and write regulatory documentation including: Technical reports, Investigator's Brochures and briefing documents
  • Investigational New Drug (IND) applications and Clinical Trial Applications (CTAs)
  • Regulatory responses and agency communications
  • Create high-quality abstracts, posters, and presentations for scientific conferences
  • Collaborate with Medical Affairs to develop scientifically accurate medical communications materials
  • Prepare scientific brochures, data summaries, and disease-state educational content
  • Support the creation of materials for advisory boards and key opinion leader (KOL) engagements
  • Contribute to medical information responses and scientific exchange materials
What we offer
What we offer
  • Opportunity to make a meaningful impact on patients living with rare bleeding disorders who have few or no treatment options
  • Collaborative, mission-driven culture with a commitment to scientific excellence
  • Work at the forefront of innovation in bleeding disorder therapeutics
  • Professional development opportunities and growth within a rapidly expanding organization
  • Fulltime
Read More
Arrow Right

R&D Knowledge and Learning Senior Manager (Content Development)

As a Senior Manager – TA/Product Knowledge & Learning (Content Development), you...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Doctorate degree with 10+ years of clinical/scientific affairs experience
  • Master’s degree with 12+ years of experience
  • Bachelor’s degree with 15+ years of experience
  • Strong experience in learning content development, visual storytelling, and instructional design
  • Proven ability to create infographics and visually compelling learning assets
  • Excellent scientific writing, editing, and presentation skills
  • Experience supporting global stakeholders in a matrixed environment
  • Strong project management and attention to detail
Job Responsibility
Job Responsibility
  • Support U.S. Senior Managers (Product/TA Learning Leads) by developing learning content aligned to product strategy and learning objectives
  • Work closely with the global K&L Sr Managers to create new learning materials while also refreshing and updating existing content
  • Design and develop a wide range of learning materials, including: Slide decks, facilitator guides, and participant materials, Infographics, visual summaries, and quick-reference tools, Content to support congress-related trainings
  • Translate complex scientific, clinical, and product information into clear, concise, and visually engaging content
  • Apply adult learning principles and instructional design best practices to enhance learner engagement
  • Incorporate interactive elements to support learning calls and virtual learning sessions
  • Manage content development timelines, version control, review cycles, and documentation
  • Review and edit content to ensure scientific accuracy, consistency, compliance, and alignment with Amgen standards
  • Incorporate feedback from U.S. Senior Managers and learners to continuously improve content quality
  • Maintain organized repositories of approved learning content and updates
Read More
Arrow Right

Medical Content Operation Manager

The Medical Content Operation Manager will be responsible for managing several p...
Location
Location
China , Hangzhou
Salary
Salary:
Not provided
pfizer.de Logo
Pfizer
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • At least 5 years of experience writing/editorial position or similar roles within online medical media environment
  • Experience in the pharmaceutical industry is a huge plus
  • Exceptional writing & editing skills and experience with multiple content formats and digital tools to facilitate efficient content production, analysis, and management
  • Deep understanding of content reader’s behavior insights & needs, with growth mindset
  • Demonstrated experience in developing high-quality content, preferably with a portfolio of published content, intended to drive customer acquisition
  • Great attention to detail and an ability to work within tight deadlines
  • Have strong esthetics taste and ability to understand the products / Therapeutic Area position and creative vision
  • Foundational knowledge of content SEO principles
  • Experience in at-scale production preferred
  • Acts decisively in complex and fast-moving environment
Job Responsibility
Job Responsibility
  • Work closely within Innovation Center with BU Digital Leads, Patient Leads and MKT, understand companywide and BU-level innovative GTM strategies, and content strategy for designated TA
  • Develop best fit HCP-facing online content plan based on business objectives and content strategy to provide exceptional medical content experience, thus making every touch point with HCP count
  • Develop patient-facing online content plan based on patient solution’s objective and content strategy to provide best contest experience to fulfill patient’s needs
  • Continuously understand reader insights and adjust content plan accordingly, ensure the agile content delivery best match with reader’s needs & industry changing trend
  • Lead and manage the agencies and editors and unify content from various contributors to ensure every piece of content lines up with content strategy, and deliverables are on time, and within budget
  • Establish end-to-end process of content production in multiple types (incl. articles, graphic, videos, etc.) to ensure excellent execution
  • Build a built-in quality control system and manage the key points of content production, as a high-level pair of eyes on each piece of content ensure accuracy and consistency
  • Monitor and plan relevant content based on certain industry-spreading topics, including topic selection and material collection and extraction, and engage with key stakeholders to drive customer acquisition
  • Participate in content operation strategies and keep evolving content processes/standards to reflect latest learnings or changes, keeping the light-speed & high-quality competency level
  • Explore innovative next-generation content production models
  • Fulltime
Read More
Arrow Right
New

Director, Medical Information

Beam is seeking a driven and scientifically rigorous Director of Medical Informa...
Location
Location
United States , Cambridge
Salary
Salary:
210000.00 - 260000.00 USD / Year
beamtx.com Logo
Beam Therapeutics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced scientific degree required: PharmD, MD, PhD, or equivalent in life sciences, pharmacy, or a related field
  • Minimum 7 years of experience in Medical Information, Medical Affairs, or Medical Communications within the pharmaceutical or biotechnology industry
  • Experience contributing to or building Medical Information capabilities, including SOP development and content library management
  • Solid working knowledge of medical review processes (MRC/PRC) and promotional/non-promotional content review, with familiarity with applicable FDA and EMA regulations
  • Strong scientific writing skills with experience developing SRDs, medical information responses, and clinical content for internal and external audiences
  • Ability to work effectively cross-functionally in a fast-paced, pre-commercial biotech environment with lean teams and evolving priorities
  • Interest in or exposure to rare disease therapeutic areas, including the scientific and operational challenges of small patient populations
  • Experience in cell and gene therapy, gene editing, or other advanced therapy medicinal products, preferred
  • Exposure to AI/ML applications in Medical Affairs or Medical Information, including prompt engineering, LLM evaluation, or AI governance, preferred
  • Familiarity with medical information platforms (e.g., Veeva Vault, Salesforce Health Cloud, MedAnswers) or emerging AI-powered MI solutions, preferred
Job Responsibility
Job Responsibility
  • Establish the Medical Information department from the ground up, including defining the operating model, staffing plan, technology infrastructure, and standard operating procedures (SOPs)
  • Develop and maintain the MI quality framework to ensure all scientific content meets regulatory, compliance, and scientific integrity standards
  • Serve as the internal subject matter expert on medical information best practices, regulatory expectations (FDA, EMA), and industry benchmarks for rare disease and advanced therapies
  • Build and oversee the medical review process for promotional and non-promotional materials, ensuring scientific accuracy and alignment with label and clinical data
  • Partner in the establishment of a Medical Review Committee (MRC) / Promotional Review Committee (PRC), collaborating closely with Regulatory Affairs, Legal, and Commercial teams
  • Create and maintain a comprehensive library of standard response documents (SRDs), custom responses, and medical FAQs covering the company's cell and gene therapy pipeline across rare disease indications
  • Author and review medical information letters, disease education materials, clinical summaries, and scientific dossiers for internal and external use
  • Ensure all MI content reflects the most current evidence base, including clinical trial data, real-world evidence, and peer-reviewed literature
  • Partner with Medical Science Liaisons (MSLs), Clinical Development, and Commercial teams to develop scientifically rigorous training materials, slide decks, and internal reference tools
  • Lead the development of pipeline and disease area resources that enable cross-functional teams to communicate accurately about the science of cell and gene therapies
  • Fulltime
Read More
Arrow Right

Team Lead - Clinical Affairs

At the forefront of health technology for over 35 years, Munich-based Brainlab d...
Location
Location
Germany , Munich
Salary
Salary:
Not provided
brainlab.com Logo
Brainlab
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced scientific, medical or technical degree (PhD, MD, or equivalent preferred)
  • Extensive experience in Clinical Affairs, Clinical Research within the medical device industry
  • Strong background in clinical and regulatory requirements for Class I–III medical devices
  • Demonstrated leadership experience, including managing international or cross-functional teams
  • Several years of experience in Clinical Affairs, Clinical Research and/or R&D within the medical device industry
  • Clinical and regulatory background for Class I to Class III medical devices
  • In-depth knowledge of EU MDR, FDA regulations and Good Clinical Practice
  • Hands-on experience in clinical studies, clinical evaluations and regulatory submissions for medical devices
  • Ability to translate clinical research into scientific marketing content
  • Excellent stakeholder management, communication, and project leadership skills
Job Responsibility
Job Responsibility
  • Define and lead the global Clinical Affairs strategy for Brainlab’s global surgery portfolio, ensuring alignment with product, regulatory and commercial objectives / teams
  • Lead and develop an international Clinical Affairs team responsible for clinical evaluation, clinical research and scientific marketing communication
  • Ensure clinical compliance with EU MDR, FDA and other regulatory requirements
  • Build and maintain a strong clinical network of investigators, key opinion leaders and research partners
  • Act as Process Owner for clinical evaluation and validation, training authors and evaluators to ensure regulatory compliance
  • Partner closely with R&D, Product Management, Marketing, Sales and Quality Management on the strategy and to translate clinical insights into product innovation and market differentiation
  • Bridge clinical research and scientific marketing by translating evidence into credible, high-impact scientific and educational content
  • Ensure GDPR compliance in clinical collaborations
  • Define and manage clinical studies and investigations to support product innovation and regulatory approvals
  • Represent the company in communications with regulatory authorities related to clinical strategy, investigations and submissions
What we offer
What we offer
  • 30 vacation days, plus December 24th and December 31st
  • Flexible working hours
  • Hybrid work model within Germany
  • Bike leasing via cooperation partner "BikeLeasing"
  • Parking garage and safe underground bike storage
  • Award-winning subsidized company restaurant and in-house cafes
  • Variety-rich fitness program in our ultra-modern 360m2 company gym
  • Regular after work, team, and company events
  • Comprehensive training and continuing education opportunities
  • Fulltime
Read More
Arrow Right

Director, Creative + Content Marketing

The Director of Creative + Content Marketing at 10x Genomics spearheads the stra...
Location
Location
United States , Pleasanton
Salary
Salary:
228300.00 - 308900.00 USD / Year
10xgenomics.com Logo
10x Genomics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 7 years in content/creative/marketing roles (science writing/editorial, copywriting, or content leadership
  • 2 years in a content or creative production team leadership role
  • Bachelor’s in scientific discipline, English, Marketing/Communications, or related field
  • Proven background in life sciences or deep technology content marketing—comfortable translating technical/scientific concepts for diverse, expert-to-nonexpert audiences
  • Strong editorial and copywriting expertise across marketing collateral, campaigns, and digital content, matched by hands-on experience creating or editing detailed science content
  • Demonstrated ability to oversee visual creative and digital production workflows (including video, graphics, and layout)
  • Excellent project management
  • able to prioritize, delegate, and deliver across multiple initiatives
  • Advanced collaboration with creative, product, and technical teams
  • able to guide concept-to-delivery for high-impact creative and written assets
Job Responsibility
Job Responsibility
  • Define and evolve the brand’s narrative, voice, and visual identity in collaboration with VP of Integrated Marketing Communications and executive leadership ensuring alignment with corporate strategy
  • Set and own the vision for all content marketing, balancing scientific rigor with creative storytelling and strong visual identity
  • Develop a multi-channel editorial and creative calendar that supports strategic campaigns, demand generation, and thought leadership
  • Collaborate with Sr. Visual Designer to guide visual/graphic design for content assets and ensure a cohesive brand experience
  • Personally take on or assign the drafting, reviewing, and refining of core content: thought leadership articles, technical blogs, whitepapers, and educational resources
  • Ensure outstanding scientific accuracy, clarity, and engagement—partnering with product, segment marketing, and internal subject matter experts
  • Lead creation and review of campaign copy, web pages, social posts, and sales collateral for consistency, clarity, and brand tone of voice
  • Oversee end-to-end production of digital (web, email, video, infographics), print, and multimedia content
  • Manage a hybrid team of in-house specialists, writers (copy and science), editors, and external agencies or freelancers
  • Own timelines, resource allocation, creative workflow, and final delivery—ensuring content is on-brand, high-quality, and on-deadline
What we offer
What we offer
  • Equity grants
  • Comprehensive health and retirement benefit programs
  • Annual bonus program or sales incentive program
  • Generous time off
  • Competitive and comprehensive health benefits package
  • Competitive easy-to-use benefits that promote wellbeing and make your life easier
  • Family friendly policies like parental leave, and other benefits
  • Fulltime
Read More
Arrow Right