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<h3>Job Description</h3>
Summary:
Entry-level Lab Scientist role within an Immunology team, ideal for recent graduates with a background in biology, immunology, or biotechnology. The position supports hands-on experimental work involving immune cell isolation, sterile cell culture, differentiation, flow cytometry, and functional immune assays.
 
Key responsibilities include isolating primary immune cells, maintaining and differentiating cell cultures, preparing and analyzing flow cytometry samples, and conducting immune cell–based functional and cytotoxicity assays. The role requires strong attention to detail, adherence to SOPs and biosafety practices, and effective collaboration within a research team.
 
Preferred candidates have exposure to immune assays, flow cytometry data analysis, and are eager to learn advanced immunology techniques in a collaborative research environment.

Biologist

<h3>Job Description</h3>
About the Role
Our client - one of the most ambitious AI research labs is hiring ML Research Scientists, Cheminformatics! With offices based in California and New York, this team is unlocking groundbreaking therapies for patients with severe diseases. They work at the intersection of machine learning, physics, and computational chemistry to advance the development of small molecule drug discovery. Backed by top investors and founded by ex-Google/Stanford Scientists, they are scaling their Cheminformatics team.
 
 
Why Join?
<ul>
<li>World-Class Research - Work alongside AI pioneers from the most elite institutions and industry labs - Google/Meta/OpenAI/Stanford/Harvard/MIT</li>
<li>Massive Compute - Unparalleled access to cutting-edge infrastructure</li>
<li>Research - this is about making fundamental advances in deep learning, representation learning, and generative models. Developing SOTA models within active drug programs, taking the lead on model validation, deployment to drive the discovery of new medicines</li>
<li>Real-World Impact - Your work won’t sit in a paper; it will be deployed in groundbreaking AI systems</li>
</ul>
 
 
Who We're Looking For:
We’re seeking top-tier ML research scientists, Cheminformatics with a strong track record of applying machine learning methods to advance small molecule drug discovery.
 
 
Your Responsibilities:
<ul>
<li>Cheminformatics expert skilled in molecular data and tools like RDKit and OpenEye.</li>
<li>Experienced in experimental drug discovery assays and CADD workflows, from docking to ADME prediction.</li>
<li>Proficient data scientist and applied ML engineer, fluent in Python, scikit-learn, and PyTorch.</li>
</ul>
 
 
What We’re Looking For:
<ul>
<li>PhD in Cheminformatics, Computational Chemistry, Computer Science</li>
<li>Expert in advanced modelling techniques, including GNNs, multitask modelling, active learning, and Bayesian optimisation.</li>
<li>Experienced in large-scale data management, SQL, data pipelines, and robust approaches to molecule featurisation and model validation.</li>
</ul>
 
 
Locations:
San Francisco, New York City
 
 
Package:
Salary up to $350,000K + benefits and equity options.
 
 
Ready to shape the future of AI? Apply now and join a team redefining intelligence.

ML Research Scientist

<h3>Job Description</h3>
Job Title: Research Assay Data Product Analyst
Location: WFH/Remote/Rahway, NJ, USA 
Duration: 11` months+ Contract
 
Notes:
Details of the request include: • Must-have skill requirements of the role: Partner with scientists and lab teams to model the assay lifecycle (design, optimization, feasibility, qualification). Understand scientific workflows—spanning assay development, validation, and configuration—into clear, actionable requirements and drive delivery with product and engineering teams. • Location / Travel – Onsite Requirements: Limited travel to Rahway, NJ; Week 1 onsite • Work Arrangement: Primarily remote after initial onsite week • Business case for Hiring Request: Need a Product Analyst experienced in R&amp;D Assay Data to translate scientific workflows into actionable requirements and collaborate with product and engineering teams. Cost efficiency is a factor. 
 
Contract description:
<ul>
<li>Collaborate with scientists and lab teams to model the assay lifecycle (design, optimization, feasibility, qualification).</li>
<li>Translate scientific workflows into clear, actionable requirements for product and engineering teams.</li>
<li>Drive delivery of data solutions that support assay development, validation, and configuration.</li>
<li>Ensure data integrity and compliance across assay-related systems and processes.</li>
<li>Monitor and optimize product performance with a focus on cost efficiency and scalability.</li>
</ul>
 
Qualifications:
<ul>
<li>Bachelor’s degree in Life Sciences, Bioinformatics, Data Science, or related field; advanced degree preferred.</li>
<li>Proven experience with R&amp;D assay data and scientific workflow modeling.</li>
<li>Strong understanding of assay development, validation, and configuration processes.</li>
<li>Ability to communicate effectively with cross-functional teams, including scientists and engineers.</li>
<li>Experience in cost analysis and delivering cost-conscious product solutions.</li>
</ul>

Research Assay Data Product Analyst

<h3>Job Description</h3>
Research Technician II — Hall Lab
 
Are you fascinated by the bizarre world of small, wiggly, often regenerative invertebrates? 
The Stowers Institute for Medical Research is seeking a Research Technician II to join the Hall Lab.
 
Our lab is motivated by the simple premise that we shouldn’t be limited to studying biology only in established “model” organisms. We are developing a suite of molecular and imaging tools to enable genetic engineering in diverse emerging model organisms, with the goal of understanding how stem cells support regeneration across the tree of life.
 
Roles &amp; Responsibilities
The selected candidate will work closely with the PI to support the lab’s research efforts by:
<ul>
<li>Developing and refining techniques to maintain and expand an array of emerging model invertebrates (with a strong emphasis on flatworms).</li>
<li>Contributing to molecular cloning that support transgenesis and gene editing strategy development.</li>
<li>Performing experiments to characterize regeneration, life history traits, and phenotype variation across species.</li>
<li>Maintaining thorough documentation (protocols, experimental records, colony/line tracking) and contributing to lab organization and best practices.</li>
</ul>
 
The ideal candidate is curious, creative, and resilient in the face of experimental setbacks. They work independently when needed, communicate clearly, and consistently incorporate feedback to improve.
 
What You’ll Be Doing
<ul>
<li>Animal husbandry to maintain several species of emerging model flatworms and related invertebrates.</li>
<li>Working with the Invertebrate Culture Facility to develop and implement more automated, standardized husbandry workflows.</li>
<li>Characterizing life-cycle traits and regenerative capabilities across diverse flatworm species (including phenotyping with immunohistochemistry and in situ hybridization, and performing genetic perturbations with CRISPR and RNAi).</li>
<li>Performing molecular cloning using techniques such as bacterial transformation, minipreps, PCR, gel electrophoresis, restriction digestion, Golden Gate assembly, and Gibson assembly.</li>
</ul>
 
 
What We Offer
<ul>
<li>Close mentorship and support to help you meet your scientific and professional goals.</li>
<li>The opportunity to work with unusual and exciting emerging model organisms in the field of regenerative biology.</li>
<li>The opportunity to work closely with our fantastic technology centers while gaining important leadership skills.</li>
<li>Professional development opportunities (lab meetings, institute seminars, and conference attendance as appropriate).</li>
<li>Competitive compensation and benefits (medical, dental, vision, 403(b)), and relocation assistance as applicable.</li>
<li>Campus perks including café access, and fitness facilities.</li>
</ul>
 
 
Minimum Qualifications
<ul>
<li>BS or MS in a relevant field (e.g., Molecular Biology, Bioengineering, Synthetic Biology, Biophysics, Chemical Biology, Ecology, Microbiology, or related discipline).</li>
<li>3+ years of laboratory experience.</li>
</ul>
 
 
Preferred Qualifications
<ul>
<li>Hands-on experience with molecular biology and/or genetics (cloning, PCR, gel electrophoresis, etc.).</li>
<li>Comfort with careful organization and recordkeeping (tracking cloning projects, animal lines, and experimental details).</li>
<li>Familiarity with sequence/plasmid design tools (e.g., Geneious, Benchling, SnapGene).</li>
<li>Imaging experience (widefield fluorescence, confocal, or similar).</li>
<li>Strong attention to detail and observational skill (e.g., recognizing “happy worms,” regeneration phenotypes, and subtle health changes).</li>
<li>A love and excitement for the organisms we work with.</li>
</ul>
 
 
How to Apply
 
Please compile the following materials into a single PDF and name the file using the format:
LastName_2026_HallLab_RTechII.pdf
 
Submit applications to: <a href="mailto:careers@stowers.org" target="_blank">careers@stowers.org</a>
 
Application materials:
<ol>
<li>Cover letter</li>
<li>Statement of career goals and research interests (1 page max)</li>
<li>Summary of prior research experience</li>
<li>CV</li>
<li>Unofficial college transcripts</li>
<li>Contact information for up to three professional references</li>
</ol>
 
We look forward to reviewing your application!

Research Technician II

<h3>Job Description</h3>
Job Description
Contact: Neisha Camacho/Terra Parsons - No 3rd party candidates Job Summary: The Biostatistician II is responsible for having a working knowledge of all related processes with the ability to independently lead a study, support analysis, and provide high-quality documents to support sponsors' research programs. The ideal candidate is a Biostatistician with strong applied SAS skills (including TFLs, inferential analyses, and randomization) who can collaborate cross-functionally with the programming team, while also independently contributing to statistical deliverables and quality review. Experience working on Phase 1 clinical trials is highly desirable, particularly with first-in-human and dose-escalation studies, including PK/PD data and early safety endpoints. Key Responsibilities
<ul>
<li>Follow department and company standard operating procedures (SOPs), forms, templates, and policies.</li>
<li>On occasion, may act as senior Biostatistician for simple to complex studies and be the central point of contact for the assigned Biostatistics team, extended internal project team, and the client.</li>
<li>Provide input for Biostatistics portion of project timelines.</li>
<li>Review protocols for simple to complex studies.</li>
<li>Generate randomization schedules using SAS or randomization-specific software.</li>
<li>Develop and QC statistical analyses for simple to complex studies.</li>
<li>Develop or assist in developing the Statistical Analysis Plans (SAPs) and related table, figure, and listing (TFL) shells.</li>
<li>Develop tables of summary statistics and graphics for clinical trials.</li>
<li>Assist in answering deficiency letters from regulatory agencies, as required.</li>
<li>Utilize SAS to validate statistician programs and results.</li>
<li>Perform QC review of analyses and documents prepared by others.</li>
<li>Oversee nonclinical projects, work with line manager to direct activities of other Biostatisticians.</li>
<li>Coordinate with internal teams to deliver quality documents on time.</li>
<li>Represent Biostatistics in client and inter-departmental meetings.</li>
<li>Conduct all work in compliance with SOPs, GCP, and regulatory guidelines.</li>
<li>Maintain familiarity with client/internal expectations and ensure aligned analyses and documentation.</li>
<li>Stay current on global regulatory requirements (FDA, EMA, ICH, GCP).</li>
<li>May participate in or lead quality improvement initiatives.</li>
<li>Other duties as assigned.</li>
</ul>

Education: Master's Degree in Statistics or a related field required.
Core Competencies
<ul>
<li>Excellent verbal and written communication</li>
<li>Ability to communicate proactively and clearly with cross-functional teams to ensure alignment on study timelines, deliverables and issues.</li>
<li>Professional attitude and strong interpersonal skills</li>
<li>Collaborative, client-focused mindset</li>
<li>Flexible with work assignments and learning</li>
<li>Strong organizational and prioritization skills</li>
<li>High attention to detail</li>
<li>Understanding of clinical research life cycle and regulations</li>
<li>Proficient in Microsoft Word, Excel, PowerPoint</li>
</ul>
Statistical &amp; Technical Skills
<ul>
<li>Own statistical deliverables from design through analysis (e.g., SAPs, TFLs)</li>
<li>Moderate SAS programming proficiency, including the ability to perform inferential statistical analyses</li>
<li>Review programming output for accuracy and alignment with SAP</li>
<li>Protocol review</li>
<li>Review of aCRF / eCRF</li>
<li>Creating and reviewing SAPs</li>
<li>Creating and writing TFL specs and shells</li>
<li>Understanding of CDISC standards (SDTM, ADaM)</li>
<li>SDTM specifications and domain review</li>
<li>ADaM specification writing and domain review</li>
<li>ADRG (Analysis Data Reviewer’s Guide) creation and review</li>
<li>Pinnacle 21 review and input</li>
</ul>

Biostatistician - Remote

<h3>Job Description</h3>
Job DescriptionSalary: $48K-$52K, depending upon experience 
Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. We can offer you the chance to build on your skills and knowledge while working among experts in their fieldsand with cutting-edge instrumentation.

Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment.We aim to recruit the best people who stand out among their peers and embody our Core Values:

<ul>
<li>Client Focused: We only succeed when our clients succeed.</li>
<li>Outstanding: We deliver meticulous results through outstanding performance.</li>
<li>Good: We act ethically and morally.</li>
<li>Employee-Centric: We honor and support our employees.</li>
<li>Nimble: We are prepared to adapt in an ever-changing industry.</li>
<li>Team-Oriented: We collaborate with each other and with our clients.</li>
</ul>
 
We currently have a role available for a Bioanalytical Chemist with industrial pharma lab experience.
 
Job duties include, but are not limited to, the following:
 
<ul>
<li>Perform routine &amp; non-routine LC/MS analyses.
<ul>
<li>Sciex/Analyst experience preferred.</li>
</ul>
</li>
<li>Develop and optimize LC/MS analytical methods.</li>
<li>Consistently produce standard curve and QC data that meet established validated assay criteria.</li>
<li>Operate and perform basic, routine maintenance and diagnostics on HPLC and mass spectrometers.</li>
<li>Use the LC/MS software to perform routine data processing.</li>
<li>Accurately prepare and label laboratory reagents, solutions and samples.</li>
<li>Consistently utilize data file nomenclature and organizational conventions.</li>
<li>Track study submissions on the analyst/customer collaboration site.</li>
</ul>
 
Job requirements include, but are not limited to:
 
<ul>
<li>BS-Chemistry (or related field) with 0-2 years of industrial experience.</li>
<li>Proactively maintaining productivity with strong attention to detail.</li>
<li>Excellent communication skills verbal and written. Ability to communicate issues as they occur.</li>
<li>Works well both as a team and as an individual.</li>
<li>Strong safety focus and willingness to assist with general lab housekeeping.</li>
<li>Ability and willingness to adapt to changing project needs and timelines.</li>
</ul>
 
This job posting will close by 2/28/2026 or when a candidate is identified, whichever comes first.

Bioanalytical Chemist

<h3>Job Description</h3>
Who we are
For 35 years, GD Barri &amp; Associates has been a trusted workforce solutions partner, delivering highly skilled engineering, technical, and professional talent to some of the nation’s most critical industries, including power, utilities, nuclear, and infrastructure. Candidates choose Barri because we offer steady opportunities, strong client relationships, and a team that truly advocates for your success. We prioritize compliance, safety, integrity, and a personalized approach that matches you with roles where your expertise is valued and your impact strengthens performance and project success from day one.
 
About the role
 
We are looking for a Chemistry Technician for a long-term contract at a power plant in Tonopah, AZ.
 
This person will provide technical, analytical and operational support to the Chemistry program. Responsible for unit operations support, instrumentation assistance, and central laboratory functions. Requires knowledge of general chemical and radiochemical principles, concepts and laboratory techniques and practices. Ability to collect, handle, and analyze environmental samples such as water, soil, and air is a plus. Must have Analytical experience.
 
Must have 2-4 years' experience as a Chemistry Technician. HS diploma required.
 
Must be able to pass the background and drug test.
 
G.D. Barri &amp; Associates, inc. is an Equal Opportunity Employer

Chemical Technician

<h3>Job Description</h3>
Job DescriptionLCMS Lead Scientist
Job Description
As a LC-MS Lead Scientist, you will play a pivotal role in overseeing bioanalytical studies, ensuring that all methods meet regulatory and client requirements. You will not be working directly in the lab but will be responsible for reviewing data, signing off on reports, and acting as the primary scientific point of contact. Your expertise will guide the bioanalytical study work, and you will coordinate with regulators and stakeholders, both internally and externally.
Responsibilities
<ul>
<li>Oversee studies and ensure all methods are prepared, validated, executed, and documented to meet regulatory and client requirements.</li>
<li>Sign off on reports and approve raw data.</li>
<li>Act as the primary scientific point of contact for studies.</li>
<li>Coach and indirectly guide a team of up to 20 members.</li>
<li>Coordinate across internal and external stakeholders, including discussions with regulators for clinical or pre-clinical studies.</li>
<li>Travel up to 10% for cross-site or client visits.</li>
</ul>
Required Skills
<ul>
<li>B.S. or Masters in Life Sciences (Chemistry, Biology, Biochemistry, etc.).</li>
<li>2-3 years of LCMS experience.</li>
<li>Experience as a Lead Scientist with 1-5 years (LS1) or 7-9 years (LS2) of experience.</li>
<li>Must have experience as a Lead Scientist/Responsible Scientist/Principle Investigator in the Bioanalytical sector (GLP or GCP regulations).</li>
<li>Full responsibility over the study, with experience in BioA CRO regulated space.</li>
<li>LBA (Ligand Binding Assay) experience, including data review/approval, protocol/sample analysis plan development, and method validation readiness.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with Sciex Mass Spec and analysis software.</li>
<li>Familiarity with LIMS, Nautilus, and Analyst software.</li>
<li>Knowledge of ICH or 28BMV regulatory guidance protocols and FDA internal standards.</li>
</ul>
Work Environment
The role is based in a lab setting within the Bioanalytical team, consisting of approximately 100 employees, including 60 chemists. This is a hybrid position, requiring 2-3 days onsite per week, with flexibility on the days but consistency each week. The role involves indirect reporting from method development chemists, validation chemists, sample analysis, and report writing. The work is workload-based rather than project-based, with a varying number of projects depending on client needs. The team is expanding, with current plans to increase from 16 to 18 members in Madison. Travel is limited, with a maximum of 10% required for client visits or conferences.
Job Type &amp; Location
This is a Permanent position based out of Madison, WI.
Pay and Benefits
The pay range for this position is $85000.00 - $110000.00/yr.
Medical Plan* No Charge Laboratory Testing Benefit and physical therapy Dental Plan Vision Plan Flexible Spending Accounts (FSAs) Health Care FSA Dependent Care FSA Disability Plan Short Term Disability (STD) Long Term Disability (LTD) Life and Accidental Death and Dismemberment (AD&amp;D) Insurance Plans Basic Life Optional Life Dependent Life Optional AD&amp;D Employee Stock Purchase Plan (ESPP)
Workplace Type
This is a hybrid position in Madison,WI.
Application Deadline
This position is anticipated to close on Jan 26, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

LCMS Lead Scientist

<h3>Job Description</h3>
PRODUCT DEVELOPMENT EPOXY CHEMIST, Rocky Hill, CT @ Henkel
YES we can assist with relocation.
 
Ideal candidate will have UV stability/ Epoxy chemistry experience.
 
What you´ll do
<ul>
<li>Design, develop, execute, and support on-time commercialization of new adhesive formulations and products.</li>
<li>Prepare and deliver presentations on research projects for internal teams, management, customers, and technical conferences.</li>
<li>Understand state-of-art technology advancement and apply it to product development. Generate new intellectual properties.</li>
<li>Perform all laboratory work in a safe manner and comply with all regulations, safety precautions, PPE requirements, and 5Sprocesses.</li>
<li>Guide and mentor junior chemists as needed.</li>
</ul>
What makes you a good fit
<ul>
<li>Master’s or PhD degree in Chemistry, Chemical Engineering, Polymer Sciences, Materials Science, or in any other related scientific areas, is highly preferred.</li>
<li>Candidate with B.S. degree and a strong track record of &gt;10 years of successful Product Development in the relevant area may be considered.</li>
<li>Proven track record of on-time product development delivery from idea generation to completion is required.</li>
<li>Minimum 5 years of experience in the areas of UV/Light stable Epoxy (1K &amp; 2K) resin for outdoor applications.</li>
<li>Strong oral and written communication skills, and excellent interpersonal skills are essential.</li>
<li>The ability to work autonomously on multiple projects is needed.</li>
<li>Traveling of up to 10% will be required.</li>
</ul>
Some perks of joining Henkel
<ul>
<li>Flexible or hybrid work model</li>
<li>Diverse national and international growth opportunities</li>
<li>Global wellbeing standards with health and preventive care programs</li>
<li>Gender-neutral parental leave for a minimum of 12 weeks</li>
<li>Employee Share Plan with voluntary investment and Henkel matching shares</li>
<li>Annual performance bonus</li>
<li>Comprehensive healthcare; mental health support &amp; 401(k) plan matched by employer</li>
<li>Family benefits including fertility support, fully paid parental leave, caregiver services</li>
<li>Paid time off: Vacations days, sick leave, holidays, volunteer time off &amp; more</li>
</ul>
 
The salary for this role is $120,000.00- $145,000.00. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range and this range. This salary range may also be modified in the future.
 
Henkel does not accept unsolicited resumes from search firms or employment agencies. Unsolicited referrals and resumes are considered Henkel property and therefore, Henkel will not pay a fee for any placement resulting from the receipt of an unsolicited referral.
 
Henkel is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information, and other legally protected categories.

Product Development Epoxy Chemist

<h3>Job Description</h3>
Analytical Chemistry- Senior Research Chemist
Exemplify BioPharma, Inc. a Symeres Company, is a global partner research organization (PRO) based in New Jersey, USA.&nbsp;We are a team of biopharma industry experts focused on delivering end-to-end Chemistry, Manufacturing and Controls (CMC) throughout the drug development and regulatory market application processes. Using a unique combination of program management, coupled with our New Jersey based process development laboratories we are ideally positioned to deliver CMC success to partner organizations.&nbsp;We are talent based team and our key asset is our experience, multidisciplinary expertise and proven track record.&nbsp;We strive to bring tangible value to our partners through provision of strategic, tactical and technical leadership to solve complex problems focused on reducing program timelines and costs.
&nbsp;
Position &amp; Responsibilities
 Exemplify BioPharma is seeking a scientific leader to serve as Senior Analytical Chemist at our R&amp;D laboratory located in Cranbury, New Jersey. The ideal candidate will have 0-3 years’ experience and a proven record of sustained laboratory achievement and innovation.
&nbsp;
The professional in this position will lead analytical development for high priority drug candidates. You will identify and characterize key physical and chemical properties of pharmaceutical materials (e.g., active drug substances) and/or formulated drug products (e.g. tablets, injectable solutions).
&nbsp;
As an innovator, you will develop, validate and implement new analytical methods to guide product development and solve challenging technical problems related to purity, stability, packaging, and manufacturing.
&nbsp;
You will define strategies to address quality-related objectives, and will recommend the methods and specifications used to monitor pharmaceutical materials and/or the formulated product. You will then lead the transfer of these technologies to CRO, CMO manufacturing sites.
&nbsp;
This professional will lead and/or participate on multi-disciplinary product development teams and will supervise the studies and professional development of one or more laboratory professionals. You will develop new scientific ideas, methods and technologies that contribute to the responsibilities described above.
&nbsp;
Other responsibilities include statistical data analysis, compliance with pharmaceutical good manufacturing practices and the completion of technical reports and external publications (as appropriate). This visible and business-critical role demands excellent oral and written communication skills.
&nbsp;
This is an exceptional opportunity for motivated candidates who wish to be exposed to all aspects of CMC drug development in a fast moving, collaborative and learning environment.
&nbsp;
Qualifications 
 A Ph.D. degree in analytical chemistry or a related discipline is preferred. The candidate must have a demonstrated ability to conduct independent research, solve scientific problems, and lead other professionals in a highly collaborative environment.
&nbsp;
 
Application
If you are interested in applying for this exciting opportunity at Exemplify BioPharma please e-mail a cover letter and resume to <a href="mailto:careers@exemplifybiopharma.com" target="_blank">careers@exemplifybiopharma.com</a>.

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