CrawlJobs Logo

Scientific Content Lead

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:

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

Briefcase Icon

Similar Jobs for Scientific Content Lead

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
New

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

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
New

Graphic Designer

Join Sanofi as Graphic Designer in our team in Barcelona. where we transform com...
Location
Location
Spain , Barcelona
Salary
Salary:
Not provided
sanofi.fr Logo
Sanofi
Expiration Date
March 31, 2026
Flip Icon
Requirements
Requirements
  • Bachelor's or Master's degree in Visual Communications, Mass Communications, Fine Arts, Communications, or related field with focus on graphic design and visualization of scientific content
  • 2-6 years of experience in graphic design, video creation, and new media
  • Proven ability to translate complex information into visual formats (videos and other visual communication methods)
  • Experience following brand guidelines while working on deliverables and preparing templates
  • Strong hands-on experience with Adobe Creative Suite: After Effects, Premiere Pro, Photoshop, Illustrator, and InDesign
  • Proficiency in Microsoft PowerPoint
  • Strong organizational and time management skills to effectively manage work activities
  • Excellent stakeholder management and communication skills (both verbal and written)
  • Ability to work independently and collaboratively within a team environment
  • Creative and aesthetic thinking with knowledge of current graphic and design trends
Job Responsibility
Job Responsibility
  • Design and produce creative deliverables including medical training and educational videos, quarterly insight videos, explainer videos, infographic animations, video publication articles, promotional videos, and animated icons
  • Develop visual materials such as PowerPoint slide decks, scientific posters, infographics, newsletters, e-mailers, flyers, brochures, and handouts following provided guidelines and specifications
  • Create interactive digital deliverables including e-learning modules and patient education materials
  • Maintain effective relationships with the Content Enhancement team, Scientific Writers in SBO, and global stakeholders to ensure scientific communication materials meet requirements
  • Collaborate with graphic designers and Scientific Writers to understand project-specific requirements and deliver requests on agreed timelines with high quality
  • Provide technical support and guidance to other graphic designers when needed
  • Prioritize and manage assigned projects, adhering to defined quality standards and delivering on time
  • Proactively communicate and flag issues to Team Lead regarding project timelines or input challenges
  • Design and set up new templates adhering to brand guidelines and manage continuity
  • Demonstrate flexibility to meet project demands and deliver outputs on time
Read More
Arrow Right

Quality Assurance Specialist, Medical Communications

Location
Location
India
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Experienced Medical Writer (1-2 years)
  • Scientific background and degree (PharmD, MD, PhD or Masters)
  • Knowledge of IT and digital solutions
  • Strong attention to detail and accuracy
  • Ability to manage and prioritize multiple, detailed activities
  • Results-orientated with fast and focused execution
  • Good communication, coordination and time management skills
  • Ability to work within a team or across multiple teams (including remotely) as well as independently
  • Fluent in oral and written English with high level of communication skills
  • Values teamwork, collaboration, and innovation
Job Responsibility
Job Responsibility
  • Cross check scientific information against cited references and ensure medical accuracy (fact check)
  • Ensure consistency with product label where applicable
  • Verify presence of essential information
  • Correct interpretation of scientific data from reference/sources
  • Alignment/formatting of content as per style guides/journal guidelines/congress guidelines
  • Ensure consistency of scientific content across different sections (including text, figures, tables)
  • Accurate bibliography/in-text citation and alignment of figures/graphs as per branding guidelines
  • Confirm that every sentence is source annotated, and each source annotation matches with respective reference and vice versa
  • Ensure that information is presented in a neutral manner without any interpretations and/or author’s conclusion
  • Track work and communicate with client team on job reviews, prioritization etc., through emails and teleconferencing if needed
Read More
Arrow Right

Senior Manager - Clinical Affairs

Define and lead the global Clinical Affairs strategy for Brainlab’s global surge...
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