{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/at/formation-bio"},"x-facet":{"type":"company","slug":"formation-bio","display":"Formation Bio","count":6},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d9e05746-2aa"},"title":"Associate Director, Bioanalytical Development","description":"<p><strong>Job Title</strong></p>\n<p>Associate Director, Bioanalytical Development</p>\n<p><strong>About Formation Bio</strong></p>\n<p>Formation Bio is a tech and AI-driven pharma company that accelerates all aspects of drug development and clinical trials.</p>\n<p><strong>About the Position</strong></p>\n<p>The Associate Director, Bioanalytical will lead bioanalytical strategy and delivery for assigned programs, working across nonclinical and clinical teams to ensure assays are fit for purpose and support key development decisions.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Lead bioanalytical strategy and delivery for assigned programs across small molecules and biologics, aligned to clinical questions and decision points</li>\n<li>Define assay plans and validation approaches (fit-for-purpose through full validation) for PK/TK, metabolites as applicable, biologics bioanalysis, and immunogenicity</li>\n<li>Manage bioanalytical CROs and specialty labs for assigned workstreams: contribute to partner selection, define scopes, set timelines, and monitor performance, quality, and budget</li>\n<li>Oversee end-to-end bioanalytical execution: protocols, validation reports, sample analysis, data review, and final reports to support program decisions and filings</li>\n<li>Own day-to-day BA operating processes for assigned programs: assay lifecycle tracking, method transfer planning, issue triage, deviation management, and CAPA follow-up with vendors</li>\n<li>Ensure data quality and audit readiness for assigned deliverables through strong documentation practices, traceability, and alignment to regulatory guidance and internal standards</li>\n<li>Partner with Clinical Pharmacology and Clinical Development on study design inputs, sampling strategies, analyte panels, and interpretation of exposure and immunogenicity implications</li>\n<li>Coordinate with Clinical Operations on sample logistics (kits, handling, stability, chain of custody, reconciliation) and resolution of operational issues impacting bioanalysis</li>\n<li>Collaborate with Regulatory Affairs by drafting/reviewing submission components and providing technical input to support IND/CTA and NDA/BLA/MAA activities</li>\n<li>Align with DMPK/Nonclinical on bioanalytical approaches across studies and support translational PK needs</li>\n<li>Work with Biostatistics/Data Science to enable clean data transfers, consistent formats/metadata, and analysis-ready datasets</li>\n<li>Support diligence and asset evaluation by reviewing bioanalytical packages, identifying gaps/risks, and proposing pragmatic remediation plans</li>\n<li>Contribute to Trial Engine scaling by helping standardize templates, workflows, and reporting conventions that improve speed and consistency across programs</li>\n</ul>\n<p><strong>About You</strong></p>\n<ul>\n<li>PhD in a relevant field with 7+ years of bioanalytical experience in biopharma, including clinical-stage support, or a relevant undergraduate degree with 10+ years of experience</li>\n<li>Lead bioanalytical strategy and execution for assigned preclinical and clinical programs across small molecules and biologics</li>\n<li>Deep LC–MS/MS expertise for PK/TK, troubleshooting, and ISR</li>\n<li>Familiar with biologics bioanalysis and immunogenicity (ADA/NAb) approaches and interpretation</li>\n<li>Strong working knowledge of bioanalytical regulatory expectations and submission-quality documentation</li>\n<li>Lead CRO/vendor execution for assigned workstreams; support partner selection and governance as needed</li>\n<li>Comfortable operating in a fast-paced, cross-functional environment with multiple concurrent priorities</li>\n<li>Clear communicator who can translate technical detail into program-relevant recommendations</li>\n<li>Preferred: Experience functioning as part of a clinical study team to integrate tradeoffs between vendor selection, development speed, assay quality and performance, and applicability of method to deliver value to program overall</li>\n<li>Preferred: Familiarity with GCP/GCLP expectations and audit/inspection readiness for clinical bioanalysis</li>\n<li>Preferred: Experience shaping sample logistics (kits, stability, chain of custody) and data flow into filings</li>\n</ul>\n<p><strong>Total Compensation Range</strong></p>\n<p>$177,500 - $232,000</p>\n<p><strong>Compensation</strong></p>\n<p>Individual compensation is determined by several factors, including role scope, geographic location, and skills &amp; experience. Your offer will reflect where you fall within the range based on these considerations. In addition to base salary, we offer equity, comprehensive benefits, and generous perks. If the posted range doesn&#39;t match your expectations, we still encourage you to apply!</p>\n<p><strong>Where We Hire</strong></p>\n<p>Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas, with a hybrid model requiring 3 days per week in office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered. Please apply only if you reside in these locations or are willing to relocate.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_d9e05746-2aa","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Formation Bio","sameAs":"https://www.formation.bio/","logo":"https://logos.yubhub.co/formation.bio.png"},"x-apply-url":"https://job-boards.greenhouse.io/formationbio/jobs/7530453","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$177,500 - $232,000","x-skills-required":["PhD in a relevant field","Bioanalytical experience in biopharma","LC–MS/MS expertise","Biologics bioanalysis and immunogenicity","Bioanalytical regulatory expectations"],"x-skills-preferred":["Experience functioning as part of a clinical study team","Familiarity with GCP/GCLP expectations","Experience shaping sample logistics and data flow"],"datePosted":"2026-04-18T15:58:11.388Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New York, NY; Boston, MA"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"PhD in a relevant field, Bioanalytical experience in biopharma, LC–MS/MS expertise, Biologics bioanalysis and immunogenicity, Bioanalytical regulatory expectations, Experience functioning as part of a clinical study team, Familiarity with GCP/GCLP expectations, Experience shaping sample logistics and data flow","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":177500,"maxValue":232000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_44d992c5-1cf"},"title":"Associate Director, Drug Product Development","description":"<p><strong>About the Position</strong></p>\n<p>The Associate Director, Drug Product, will provide strategic and hands-on operational leadership for all CMC activities related to drug product development and manufacturing, with a primary focus on sterile injectables (lyophilized and liquid) at all stages of development (IND-enabling to commercialization).</p>\n<p><strong>Responsibilities</strong></p>\n<p><strong>Development and Manufacturing Strategy, Operations and Oversight</strong></p>\n<ul>\n<li>Lead drug product manufacturing strategy and execution for programs from preclinical through commercial stages, ensuring alignment with program objectives, timelines, and budget constraints.</li>\n</ul>\n<ul>\n<li>Serve as the primary technical interface with CDMOs and contract manufacturing organizations for drug product manufacturing activities. Establish and maintain strong partnerships, lead technical discussions, and ensure manufacturing excellence across external manufacturing networks.</li>\n</ul>\n<ul>\n<li>Oversee formulation, aseptic fill-finish, lyophilization (if applicable), visual inspection, labeling, and packaging operations for drug products. Ensure manufacturing processes are robust, scalable, and compliant with cGMP requirements.</li>\n</ul>\n<ul>\n<li>Provide technical guidance and oversight for manufacturing campaigns including batch record review and approval, deviation investigations, change control assessments, and resolution of manufacturing issues</li>\n</ul>\n<ul>\n<li>Support scale-up activities from clinical to commercial manufacturing, including process optimization and validation. Identify and implement continuous improvement opportunities.</li>\n</ul>\n<ul>\n<li>Develop comprehensive manufacturing plans and schedules in collaboration with Project Management, Clinical Supply, and Commercial teams. Track manufacturing timelines and proactively manage risks to ensure on-time delivery of drug product for clinical trials and commercial supply.</li>\n</ul>\n<ul>\n<li>Lead technical assessments and qualification of new CDMOs for drug product manufacturing. Conduct site audits and ongoing performance monitoring. Manage relationships with multiple manufacturing partners across different geographic regions</li>\n</ul>\n<p><strong>Additional Core CMC Responsibilities (Quality, Regulatory &amp; Cross-Functional)</strong></p>\n<ul>\n<li>Ensure all manufacturing activities comply with cGMP regulations, ICH guidelines, and internal quality standards. Support regulatory inspections and audits at manufacturing sites. Review and approve batch records, protocols, and manufacturing-related documentation.</li>\n</ul>\n<ul>\n<li>Author and review CMC sections of regulatory submissions (INDs, BLAs, CTAs) related to drug product manufacturing, process validation, and manufacturing site changes. Support responses to health authority questions.</li>\n</ul>\n<ul>\n<li>Partner closely with Drug Substance Manufacturing, Analytical Development, Quality Assurance, Regulatory Affairs, Clinical Supply, and Project Management leads to ensure seamless integration of manufacturing activities into overall program execution.</li>\n</ul>\n<ul>\n<li>Collaborate with procurement to ensure timely contracting for drug product manufacturing.</li>\n</ul>\n<p><strong>About You</strong></p>\n<ul>\n<li>MS or Ph.D. in Chemical Engineering, Pharmaceutical Sciences, Biochemistry, Biotechnology, or related discipline.</li>\n</ul>\n<ul>\n<li>6+ years of experience in the biopharmaceutical industry with hands-on experience in biologics drug product manufacturing, formulation development, and fill-finish operations.</li>\n</ul>\n<ul>\n<li>Demonstrated track record of successfully managing drug product manufacturing campaigns for biologics (proteins, monoclonal antibodies, antibody-drug conjugates, or other large molecules) from preclinical through late-stage clinical or commercial manufacturing.</li>\n</ul>\n<ul>\n<li>Technical expertise in aseptic fill-finish operations, lyophilization processes, formulation development, stability programs, and drug product characterization for biologics.</li>\n</ul>\n<ul>\n<li>Extensive experience working with CDMOs and contract manufacturing organizations, including site selection, technology transfers, manufacturing oversight, and performance management. Proven ability to troubleshoot complex manufacturing issues and drive continuous improvement initiatives.</li>\n</ul>\n<ul>\n<li>Strong knowledge of cGMP regulations, FDA and EMA guidelines, ICH quality guidelines, and regulatory expectations for drug product manufacturing.</li>\n</ul>\n<ul>\n<li>Experience authoring and reviewing CMC sections of regulatory submissions (INDs, BLAs, CTAs) related to drug product manufacturing and validation activities.</li>\n</ul>\n<ul>\n<li>Strong project management skills with demonstrated ability to manage multiple manufacturing programs simultaneously, meet aggressive timelines, and navigate competing priorities.</li>\n</ul>\n<ul>\n<li>Excellent communication and interpersonal skills with ability to influence and build strong relationships with internal stakeholders and external manufacturing partners.</li>\n</ul>\n<ul>\n<li>Willingness to travel domestically and internationally (approximately 20-30%) to manufacturing sites for audits, manufacturing oversight, and technical meetings.</li>\n</ul>\n<p><strong>Total Compensation Range</strong></p>\n<p>$177,000 - $235,000</p>\n<p><strong>Where We Hire</strong></p>\n<p>Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas, with a hybrid model requiring 3 days per week in office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered. Please apply only if you reside in these locations or are willing to relocate.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_44d992c5-1cf","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Formation Bio","sameAs":"https://www.formation.bio/","logo":"https://logos.yubhub.co/formation.bio.png"},"x-apply-url":"https://job-boards.greenhouse.io/formationbio/jobs/7529160","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$177,000 - $235,000","x-skills-required":["biologics drug product manufacturing","formulation development","fill-finish operations","aseptic fill-finish operations","lyophilization processes","stability programs","drug product characterization","cGMP regulations","FDA and EMA guidelines","ICH quality guidelines","regulatory expectations for drug product manufacturing"],"x-skills-preferred":[],"datePosted":"2026-04-18T15:57:56.146Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New York, NY; Boston, MA"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Healthcare","skills":"biologics drug product manufacturing, formulation development, fill-finish operations, aseptic fill-finish operations, lyophilization processes, stability programs, drug product characterization, cGMP regulations, FDA and EMA guidelines, ICH quality guidelines, regulatory expectations for drug product manufacturing","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":177000,"maxValue":235000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_f10f46f0-563"},"title":"Director, Business Development - Search & Evaluation","description":"<p>We are seeking a Director of Business Development, Strategic Sourcing to play a key role in identifying, evaluating, and managing early-stage assets and opportunities for our business development pipeline.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Lead deal-by-deal opportunity/asset teams from asset identification to transaction close</li>\n<li>Collaborate with the BD team to identify target areas for outreach, focusing on strategic alignment with our goals</li>\n<li>Own and manage one or more designated business development outreach areas</li>\n<li>Maximise activity and ensure high-quality deal flow in assigned outreach areas</li>\n<li>Conduct initial triage of opportunities, evaluating potential deals before engaging the broader diligence team to ensure strategic fit</li>\n</ul>\n<p>About You: The ideal candidate will have a strong scientific background paired with business acumen, ideally with experience in search and evaluation, venture, or business development.</p>\n<ul>\n<li>PhD in biological science or MD with laboratory research experience strongly preferred</li>\n<li>3-7 years of post-degree experience, with a combination of scientific and business expertise</li>\n<li>Prior experience of biotech or pharmaceutical business development (search &amp; evaluation), venture capital investing, or life sciences consulting is highly preferable</li>\n<li>Strong network within the biotech and pharmaceutical industries, with the ability to leverage contacts for sourcing early-stage assets</li>\n</ul>\n<p>This role offers the opportunity to help build the pharma company of the future, combining strategic asset acquisition with tech-enabled development capabilities to bring new treatments to patients faster and more efficiently.</p>\n<p>Total Compensation Range: $228,000 - $310,000</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_f10f46f0-563","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Formation Bio","sameAs":"https://www.formation.bio/","logo":"https://logos.yubhub.co/formation.bio.png"},"x-apply-url":"https://job-boards.greenhouse.io/formationbio/jobs/7589988","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$228,000 - $310,000","x-skills-required":["business development","pharmaceuticals","biotechnology","venture capital","life sciences"],"x-skills-preferred":["AI","drug development","clinical trials","networking","relationship building"],"datePosted":"2026-04-18T15:55:33.888Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Boston, MA"}},"employmentType":"FULL_TIME","occupationalCategory":"Business Development","industry":"Pharmaceuticals","skills":"business development, pharmaceuticals, biotechnology, venture capital, life sciences, AI, drug development, clinical trials, networking, relationship building","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":228000,"maxValue":310000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_d5954a0d-cd7"},"title":"Associate Director, Analytical Development & QC","description":"<p><strong>Job Title</strong></p>\n<p>Associate Director, Analytical Development &amp; QC</p>\n<p><strong>About the Position</strong></p>\n<p>We are seeking a highly motivated, self-driven and detail-oriented Associate Director of Analytical Development and Quality Control to join our CMC team.</p>\n<p>This role will provide broad exposure across Formation Bio&#39;s portfolio, requiring the ability to flex between small molecule and biologics programs at different phases of development in an outsourced development model, requiring strong technical skillset, vendor management, and the ability to balance scientific rigor with program timelines.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>In close collaboration with CDMOs and contract testing laboratories, lead development, optimisation and validation of phase-appropriate analytical methods for small molecule and biologics drug substances and drug products.</li>\n<li>Manage testing (in-process, release, stability) at CDMOs and contract testing laboratories.</li>\n<li>Provide technical oversight for method transfers, comparability assessments, and laboratory readiness.</li>\n<li>Lead selection, qualification, and ongoing performance management of external analytical vendors.</li>\n<li>Oversee and manage Formation Bio&#39;s stability studies across all programs, including review and approval of stability protocols and review and trending of stability data to support shelf-life and retest dating. Track and publish stability program metrics. Act as the primary contact for stability-related inquiries.</li>\n<li>Oversee and manage Formation Bio&#39;s critical reagents and reference standards inventory and testing.</li>\n<li>Lead investigations of release and stability OOS and OOT results, deviations, CAPAs and change controls.</li>\n<li>Author and review analytical sections of CMC documents, including protocols, reports, and regulatory submissions.</li>\n<li>Author and review of SOPs and work instructions.</li>\n<li>Closely collaborate with CMC, QA, and Regulatory teams.</li>\n</ul>\n<p><strong>About You</strong></p>\n<ul>\n<li>Analytical Chemistry, Biochemistry, Molecular Biology, or a related discipline Master&#39;s degree with 5+ years or Bachelor&#39;s Degree with 8+ years of relevant small molecule and biologics analytical development and QC experience.</li>\n<li>Proven ability to operate effectively in a fast-paced, virtual, and outsourced development environment.</li>\n<li>Highly organised with a track record of managing multiple priorities across programs in an outsourced development model.</li>\n<li>Strong scientific judgement with the ability to independently assess data quality, identify risks, and recommend mitigation strategies.</li>\n<li>Ability to communicate complex analytical concepts clearly to both technical and non-technical stakeholders.</li>\n<li>Collaborative mindset with a strong sense of ownership and accountability.</li>\n<li>Extensive hands-on experience developing, optimising, and validating analytical methods for release and stability testing of small molecules and biologics.</li>\n<li>Hands-on experience with analytical methods pertinent to bilogics (qPCR, IEF, UHPLC, MS, CE, SDS-PAGE, ELISA, peptide mapping, glycan analysis, etc.) and small molecules (UHPLC, IC, GC, IR, UV, KF, PSD, dissolution, etc.).</li>\n<li>Experience with authoring and reviewing technical documents such as test methods, method development reports, validation protocols, validation reports, specification justification reports, retest and shelf-life memos, and SOPs.</li>\n<li>Experience with designing stability studies and performing stability data trending according to applicable guidances.</li>\n<li>Strong working knowledge of Smartsheet and JMP.</li>\n<li>Thorough understanding of ICH, FDA, EMA guidances and GMP requirements governing process development, manufacturing, and stability.</li>\n<li>Ability to travel domestically and internationally up to 25% of the time.</li>\n</ul>\n<p><strong>Total Compensation Range</strong></p>\n<p>$177,000 - $235,000</p>\n<p><strong>Where We Hire</strong></p>\n<p>Formation Bio is prioritising hiring in key hubs, primarily the New York City and Boston metro areas, with a hybrid model requiring 3 days per week in office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered. Please apply only if you reside in these locations or are willing to relocate.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_d5954a0d-cd7","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Formation Bio","sameAs":"https://www.formationbio.com/","logo":"https://logos.yubhub.co/formationbio.com.png"},"x-apply-url":"https://job-boards.greenhouse.io/formationbio/jobs/7529162","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$177,000 - $235,000","x-skills-required":["Analytical Chemistry","Biochemistry","Molecular Biology","Small Molecule Analysis","Biologics Analysis","Method Development","Method Validation","Stability Testing","Quality Control","Regulatory Compliance","ICH Guidelines","FDA Guidelines","EMA Guidelines","GMP Requirements"],"x-skills-preferred":["Smartsheet","JMP","qPCR","IEF","UHPLC","MS","CE","SDS-PAGE","ELISA","Peptide Mapping","Glycan Analysis"],"datePosted":"2026-04-18T15:54:49.357Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New York, NY; Boston, MA"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Technology","skills":"Analytical Chemistry, Biochemistry, Molecular Biology, Small Molecule Analysis, Biologics Analysis, Method Development, Method Validation, Stability Testing, Quality Control, Regulatory Compliance, ICH Guidelines, FDA Guidelines, EMA Guidelines, GMP Requirements, Smartsheet, JMP, qPCR, IEF, UHPLC, MS, CE, SDS-PAGE, ELISA, Peptide Mapping, Glycan Analysis","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":177000,"maxValue":235000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_54f58a4d-707"},"title":"Senior Data Scientist","description":"<p>As a Senior Data Scientist at Formation Bio, you will be at the forefront of revolutionizing drug development through AI and advanced analytics. In this role, you&#39;ll lead crucial initiatives that directly impact our drug development portfolio, from developing sophisticated models for patient selection to creating AI-powered solutions for clinical trial optimization.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Lead and execute complex data science projects that directly advance our drug development portfolio</li>\n<li>Develop and implement sophisticated models for therapeutic hypothesis evaluation, including patient stratification and biomarker identification</li>\n<li>Design and create AI models for modernizing clinical trial evaluations, including surrogate endpoints</li>\n<li>Aid in the development and training of AI agents to automate and optimize biomedical workflows</li>\n<li>Collaborate cross-functionally with clinical, technical, and research teams</li>\n<li>Present complex analytical findings to senior stakeholders, including executive leadership</li>\n</ul>\n<p>About You:</p>\n<ul>\n<li>Required Qualifications:</li>\n</ul>\n<p>+ PhD in computational sciences or life sciences   + 3+ years of post-academic experience in life sciences (biotech, pharma, consulting)   + Strong programming skills, particularly in Python   + Extensive experience in multi-modal bioinformatics analysis</p>\n<ul>\n<li>Preferred Qualifications:</li>\n</ul>\n<p>+ Proven expertise in cloud computing environments, including proficiency with tabular and/or graph databases   + Strong background in machine learning and deep learning, particularly in biological applications   + Experience with large language models (LLM)   + Demonstrated ability to collaborate effectively with engineering teams on production systems   + Strong communication skills with proven ability to present complex technical findings to senior stakeholders</p>\n<p>Total Compensation Range: $170,000 - $215,000</p>\n<p>Where We Hire:</p>\n<p>Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas, with a hybrid model requiring 3 days per week in office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_54f58a4d-707","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Formation Bio","sameAs":"https://www.formation.bio/","logo":"https://logos.yubhub.co/formation.bio.png"},"x-apply-url":"https://job-boards.greenhouse.io/formationbio/jobs/6623947","x-work-arrangement":"hybrid","x-experience-level":"senior","x-job-type":"full-time","x-salary-range":"$170,000 - $215,000","x-skills-required":["PhD in computational sciences or life sciences","3+ years of post-academic experience in life sciences (biotech, pharma, consulting)","Strong programming skills, particularly in Python","Extensive experience in multi-modal bioinformatics analysis"],"x-skills-preferred":["Proven expertise in cloud computing environments, including proficiency with tabular and/or graph databases","Strong background in machine learning and deep learning, particularly in biological applications","Experience with large language models (LLM)","Demonstrated ability to collaborate effectively with engineering teams on production systems","Strong communication skills with proven ability to present complex technical findings to senior stakeholders"],"datePosted":"2026-04-18T15:53:58.264Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New York, NY; Boston, MA"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Healthcare","skills":"PhD in computational sciences or life sciences, 3+ years of post-academic experience in life sciences (biotech, pharma, consulting), Strong programming skills, particularly in Python, Extensive experience in multi-modal bioinformatics analysis, Proven expertise in cloud computing environments, including proficiency with tabular and/or graph databases, Strong background in machine learning and deep learning, particularly in biological applications, Experience with large language models (LLM), Demonstrated ability to collaborate effectively with engineering teams on production systems, Strong communication skills with proven ability to present complex technical findings to senior stakeholders","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":170000,"maxValue":215000,"unitText":"YEAR"}}},{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_62b851a9-660"},"title":"Data Scientist","description":"<p>Job Title: Data Scientist</p>\n<p><strong>About the Position</strong></p>\n<p>As a Data Scientist on the platform prediction team, you will translate our probability of success predictions into measurable portfolio-level outcomes. You will architect core systems that let us rigorously evaluate signals from our AI-driven predictions in public and private equities and our internal portfolio.</p>\n<p>This role sits at the intersection of quantitative finance, healthcare data, and AI-driven drug development. If you&#39;re excited about applying portfolio construction and risk management fundamentals to one of the most consequential prediction problems in healthcare, this is the role.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Work with the team to implement and maintain core portfolio engine: order management system, execution simulation layer, portfolio construction service, and performance tracking</li>\n<li>Design risk frameworks that quantify exposure across a portfolio of drug development bets with radically different risk profiles, timelines, and failure modes</li>\n<li>Run rigorous backtesting experiments with strict temporal constraints to evaluate Formation strategies against baseline approaches and measure marginal signal from new evidence sources</li>\n<li>Coordinate across the organization to integrate internal Formation data sources (clinical trial data, genomic evidence, real-world data) and proprietary tooling into portfolio analytics pipelines</li>\n<li>Work with product and engineering teams to build dashboards and reporting that communicate portfolio performance, risk metrics, and strategy comparisons to both technical and executive stakeholders</li>\n<li>Collaborate with the broader data science team to ensure portfolio-level evaluation feeds back into model improvement and evidence prioritization</li>\n</ul>\n<p><strong>About You</strong></p>\n<p>We are looking for a highly motivated and experienced Data Scientist to join our team. The ideal candidate will have a strong background in data science, machine learning, and software development, with a proven track record of delivering high-quality results in a fast-paced environment.</p>\n<p><strong>Requirements</strong></p>\n<ul>\n<li>MS or PhD in a quantitative field (statistics, finance, physics, computational science, engineering, or related)</li>\n<li>1-3 years in a quantitative research, data science, or analytics role , finance, healthcare, academic research, or consulting all count; substantive internships qualify</li>\n<li>Strong Python programming skills with experience in data-intensive workflows (pandas, numpy, scipy)</li>\n<li>Solid grasp of core portfolio construction and risk concepts: position sizing, rebalancing, Sharpe ratio, drawdown, volatility, benchmark comparison</li>\n<li>Demonstrated ability to work with messy, real-world datasets , comfortable with data wrangling, deduplication, and quality assessment</li>\n<li>Clear communicator who can present quantitative results to both technical peers and business stakeholders</li>\n</ul>\n<p><strong>Preferred Qualifications</strong></p>\n<ul>\n<li>Experience with backtesting frameworks or portfolio simulation (vectorbt, Backtrader, or custom implementations)</li>\n<li>Exposure to healthcare, pharma, or biotech data (clinical trials, claims data, -omics, real-world evidence)</li>\n<li>Familiarity with alternative data in a research or investment context</li>\n<li>Experience with probability-of-success modeling, drug development decision analysis, or health economics</li>\n<li>Comfort with LLMs or AI/ML pipelines in a production or research setting</li>\n<li>Familiarity with dashboard/visualization tools (Streamlit, Plotly, Dash) and pipeline orchestration (Dagster, Airflow)</li>\n</ul>\n<p><strong>Total Compensation Range:</strong> $154,500 - $202,000</p>\n<p>**Compensation Individual compensation is determined by several factors, including role scope, geographic location, and skills &amp; experience. Your offer will reflect where you fall within the range based on these considerations. In addition to base salary, we offer equity, comprehensive benefits, and generous perks. If the posted range doesn&#39;t match your expectations, we still encourage you to apply!</p>\n<p>**Where We Hire Formation Bio is prioritizing hiring in key hubs, primarily the New York City and Boston metro areas, with a hybrid model requiring 3 days per week in office. Applicants from the Research Triangle (NC) and San Francisco Bay Area may also be considered. Please apply only if you reside in these locations or are willing to relocate.</p>\n<p style=\"margin-top:24px;font-size:13px;color:#666;\">XML job scraping automation by <a href=\"https://yubhub.co\">YubHub</a></p>","url":"https://yubhub.co/jobs/job_62b851a9-660","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Formation Bio","sameAs":"https://www.formation.bio/","logo":"https://logos.yubhub.co/formation.bio.png"},"x-apply-url":"https://job-boards.greenhouse.io/formationbio/jobs/7757667","x-work-arrangement":"hybrid","x-experience-level":"mid","x-job-type":"full-time","x-salary-range":"$154,500 - $202,000","x-skills-required":["Python","pandas","numpy","scipy","portfolio construction","risk management","backtesting","data wrangling","data visualization"],"x-skills-preferred":["backtesting frameworks","portfolio simulation","healthcare data","alternative data","probability-of-success modeling","drug development decision analysis","health economics","LLMs","AI/ML pipelines","dashboard/visualization tools","pipeline orchestration"],"datePosted":"2026-04-18T15:53:29.085Z","jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"New York, NY; Boston, MA"}},"employmentType":"FULL_TIME","occupationalCategory":"Engineering","industry":"Healthcare","skills":"Python, pandas, numpy, scipy, portfolio construction, risk management, backtesting, data wrangling, data visualization, backtesting frameworks, portfolio simulation, healthcare data, alternative data, probability-of-success modeling, drug development decision analysis, health economics, LLMs, AI/ML pipelines, dashboard/visualization tools, pipeline orchestration","baseSalary":{"@type":"MonetaryAmount","currency":"USD","value":{"@type":"QuantitativeValue","minValue":154500,"maxValue":202000,"unitText":"YEAR"}}}]}