field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job DescriptionJob Title: Clean Room Operator - $22-24/hrJob Description
Aerotek is hiring immediately! We are looking for a dedicated Clean Room Operator to join our team. The ideal candidate will be flexible with overtime and possess a strong attendance and reliability record. This role requires the ability to stand for the entire shift, work with small hand tools and components, and multitask across multiple workstations. Our company is in its early stages, and we are seeking individuals who are willing to wear many hats and grow with us. This position is full time offering competitive pay and benefits!
Responsibilities
<ul>
<li>Manufacture, inspect, and package products following written processes.</li>
<li>Work at a pace that meets established time standards while ensuring quality.</li>
<li>Identify quality issues or workmanship deficiencies related to equipment, assembly, inspection processes, materials, and the manufacturing environment.</li>
<li>Comply with cGMP requirements by maintaining individual training records and adhering to documented manufacturing practices and procedures as defined in quality systems procedures.</li>
<li>Maintain a clean, safe, and organized work environment.</li>
<li>Comply with all policies and procedures.</li>
<li>Perform other duties as assigned.</li>
</ul>
 Pay and Benefits
The pay range for this position is $22.00 - $24.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Lowell,MA.
Application Deadline
This position is anticipated to close on May 14, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Operator

<h3>Job Description</h3>
Job Description
Responsibilities:
<ul>
<li>Perform basic cell line development (CLD) techniques and generate stable cell lines using transfection, transduction, selection, single cell subcloning, growth and expression screening, cell banking and stability assessment.&nbsp;</li>
<li>Support molecular and genetic characterization of producer cell lines and leverage these findings for the development of novel cell line substrates.&nbsp;</li>
<li>Contribute towards the design and implementation of new technologies and genome engineering strategies to support CLD platform innovation.&nbsp;</li>
<li>Maintain accurate and detailed laboratory notebooks and electronic records.&nbsp;</li>
<li>Interpret project results and contribute to technical discussions by effectively communicating key updates to collaborators and team members.&nbsp;</li>
<li>Capability to work independently and manage multiple projects. &nbsp;</li>
<li>Highly organized with strong attention to detail, accuracy, and conciseness. &nbsp;</li>
<li>Excellent analytical and problem-solving skills. &nbsp;</li>
<li>Strong planning skills and a history of meeting accelerated timelines.&nbsp;</li>
<li>Demonstrate a strong sense of work ethic and agility in a dynamic, cross-functional, collaborative environment.&nbsp;</li>
</ul>
 Basic Qualification:&nbsp;
<ul>
<li>Ph.D., MS, or BS degree in Biochemistry, Cell Biology, Molecular Biology, Bioengineering or relevant fields with 0-2yr (PhD), 2-4yr (MS), 3-5yr (BS) years of relevant experience within a pharmaceutical or biotech industry.&nbsp;</li>
<li>Extensive experience with mammalian cell culture (adherent and suspension) with strong aseptic techniques required. &nbsp;&nbsp;</li>
<li>Hands-on experience in Cell Line development is preferred&nbsp;</li>
<li>Proven expertise in molecular biology assays such as DNA/RNA extraction, PCR, Sanger Sequencing, qPCR/ddPCR/dPCR for viral titer, copy number and transcript analysis, Western blot, Flow cytometry required. Hands-on experience with laboratory instrumentation such as JESS, WES, Attune NxT, Chemometec NC3000, Refeyn, Incucyte, VIPS single-cell seeder is preferred.&nbsp;</li>
<li>Experience in upstream processes like virus production, purification, and characterization protocols preferred.&nbsp;</li>
<li>Experience using genome editing tools (CRISPR and transposases) to modify mammalian cell lines preferred.&nbsp;</li>
<li>Experience analyzing some/all the following platforms: whole-genome/exome sequencing, RNA-sequencing (e.g., Illumina), single-cell/nucleus RNA-seq (10x Genomics), High-throughput library-based discovery, and long-read sequencing (e.g., PacBio and Oxford Nanopore)&nbsp;</li>
<li>Proficiency with Microsoft Office Suite and GraphPad Prism, and familiarity with additional software such as SW compass, QuantStudio, Snapgene, and GeneiousPrime.&nbsp;</li>
</ul>
 “Nice-to-have” Qualifications:&nbsp;
<ul>
<li>Familiarity with biological annotation and ontology resources, such as Ensembl, GO, and UniProt&nbsp;</li>
<li>Experience using Java, JavaScript, Python, R, Scala, or SQL to organize and analyze complex data sets&nbsp;</li>
<li>A background in neuroscience and/or virology&nbsp;</li>
</ul>
Company DescriptionThe Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire &amp; Contract Consultants) and Retained Executive Search. 
<h3>Company Description</h3>
The Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire &amp; Contract Consultants) and Retained Executive Search.

Cell Line Development Associate

<h3>Job Description</h3>
Job Description
Job Title:
Senior Associate Scientist II - Protein Scientist
Reports to (title):
Xiaofei E, Senior Principal Scientist, Molecular Therapeutics
Solid Summary:
Solid Biosciences is a life science company focused on advancing a portfolio of neuromuscular and cardiac programs, including SGT-003, a differentiated gene therapy candidate for the treatment of Duchenne, SGT212, a gene therapy program for the treatment of Friedreich’s Ataxia, SGT-501, a gene therapy program for the treatment of catecholaminergic polymorphic ventricular tachycardia, SGT-401 a gene therapy program for the treatment of BAG3 mediated dilated cardiomyopathy, and additional assets for the treatment of fatal cardiac diseases. Solid aims to be the center of excellence across a given disease spectrum bringing together those with expertise in science, technology, disease management, and care. Patient-focused and founded by those directly impacted, Solid’s mandate is to improve the daily lives of patients living with these devastating diseases.
Position Summary:
We are seeking a skilled and motivated associate scientist to join the Molecular Therapeutics team to purify AAV libraries and to define the mechanism of transduction of selected capsids. The ideal candidate will have a strong background in protein science including protein binding assays, protein structure, and cell biology. 
Key Duties &amp; Accountabilities:
<ul>
<li>Optimize methods for production and isolation of AAV capsid libraries using automated liquid handlers such as Tecan</li>
<li>In vitro AAV transduction experiments in normal and CRISPr KO cells</li>
<li>Protein binding and inhibition experiments</li>
<li>Contribute to modelling of protein structures</li>
<li>Collaborate within the molecular therapeutics team and across the R&amp;D organization including computational biologists, analytical development, and process development</li>
<li>Communicate findings and insights to stakeholders through reports, presentations, and visualizations.</li>
</ul>
Core Competencies Required:
<ul>
<li>Experience with AAV and/or antibody production and drug development</li>
<li>Strong technical skills in protein biochemistry and cell biology to define the mechanism of AAV transduction </li>
<li>Proficiency in computing include Geneious, BLAST, Ensembl, NCBI, Uniprot, USCS, GTEx, Microsoft, PRISM statistics program </li>
<li>Candidates with experience in molecular modeling such as alpha-fold, DynamicBind, or equivalent will be preferred </li>
<li>Strong problem-solving skills and the ability to work independently and collaboratively.</li>
<li>Excellent communication and presentation skills.</li>
</ul>
Knowledge: Education, Experience, &amp; Skills:
Bachelor of Science with either a Master’s degree and/or 3 years’ industry experience in protein science research
Travel Commitment:
Solid Biosciences, Charlestown, MA
Role Location 
(HQ, Hybrid, Remote, NC, etc.)
HQ

Senior Associate Scientist II-Protein Scientist

<h3>Job Description</h3>
Job Description
Company Overview 
1910 Genetics is a Series A stage biotechnology company that is pioneering a novel Input-Transform-Output (ITO™) platform as the first ever horizontal AI infrastructure for drug discovery. 
In a crowded space with hundreds of AI drug discovery companies, 1910's ITO™ platform is differentiated by: 
<ul>
<li>Modality agnostic drug discovery: our platform is capable of designing both small molecule and large molecule therapeutics across all disease areas, with an initial focus on neuroscience, oncology, and autoimmune diseases.</li>
<li>Proprietary massive multimodal data, which overcomes the data scarcity problem that prevents frontier AI models from being utilized for drug discovery.</li>
<li>Multi-AI agent systems that include a robust collection of frontier AI/ML models, each of which works in a task-oriented manner to achieve the multi-parameter optimization problem of drug discovery and development.</li>
<li>A state-of-the-art (SOTA) fully-automated, high throughput wet laboratory in the premier Boston Seaport District for both data generation for AI model training as well as validation of the safety and efficacy of drug candidates that are outputted by our frontier AI models.</li>
<li>An unprecedented partnership with Microsoft, which positions 1910 as the only biotech/pharma company leveraging Azure Quantum Elements, a groundbreaking, AI-driven, high performance computing (HPC) cloud architecture for advanced AI.</li>
<li>Bespoke conversational AI chatbots that provide a customer friendly UI/UX to access our platform for specific drug discovery tasks.</li>
<li>Being the only biotech company helping pharma companies integrate 6 core areas of AI infrastructure.</li>
</ul>
1910 Genetics is looking for an In Vitro Pharmacology Assay Scientist to work closely with our biologists in the discovery of antibodies. An expert in biochemical characterization of biological drug molecules, the ideal candidate will have experience in antibody drug discovery and characterization of a variety of molecular types. 
Role Responsibilities 
<ul>
<li>Validate target material in functional biochemical assays prior to the start of antibody discovery. </li>
</ul>
<ul>
<li>Design, validate and execute in vitro biochemical assays for the screening of molecules from 1910 Genetics' AI-driven large molecule therapeutics platform </li>
</ul>
<ul>
<li>Develop, validate and execute assays for the biophysical characterization of antibodies in various formats and for various modalities </li>
</ul>
<ul>
<li>Work closely with 1910 scientists to refine assays to help drive delivery of program objectives </li>
</ul>
<ul>
<li>Maintain detailed records of experimental procedures and results in electronic lab notebook </li>
</ul>
<ul>
<li>Present experimental results/progress in a timely manner and contribute to scientific discussion in group meetings </li>
</ul>
<ul>
<li>Collaborate with cross-functional teams, including AI Research and Computational Chemistry to discuss project updates as well as ensure the project milestones and timelines are met </li>
</ul>
<ul>
<li>Assist laboratory operations, including maintenance of equipment, reagent tracking and monthly inspections for safety equipment </li>
</ul>
<ul>
<li>Develop and execute standard operating procedures and best practices to enhance lab efficiency and productivity </li>
</ul>
<ul>
<li>Contribute to the preparation of scientific reports, presentations, and publications. </li>
</ul>
<ul>
<li>Provide intellectual input into small molecule projects when required </li>
</ul>
<ul>
<li>Stay current with scientific literature and emerging technologies in the fields of large and small molecule research </li>
</ul>
Qualifications
<ul>
<li>PhD in Biology with a focus on Biochemistry, Cell Biology, In Vitro Pharmacology, Biomedical Sciences or a related field </li>
</ul>
<ul>
<li>Postdoctoral experience or relevant industry experience in drug discovery or In Vitro Pharmacology </li>
</ul>
<ul>
<li>Experience in developing, validating and implementing biology, biochemical, and cell-based assays </li>
</ul>
<ul>
<li>Familiarity with signal transduction pathways in relevant therapeutic areas such as Immunology &amp; Inflammation, neuroscience, oncology, and cardiomedabolic diseases </li>
</ul>
<ul>
<li>Experience with immune cell isolation and assay development </li>
</ul>
<ul>
<li>Experience using analytical techniques/instrumentation for characterization and quantification of large molecules, including chromatographic techniques such as HIC (Hydrophobic Interaction Chromatography) and RP (Reverse Phase), SEC (Size Exclusion Chromatography), SDS-PAGE, UV-Vis, etc. </li>
</ul>
<ul>
<li>Familiarity with conjugation, purification and characterization of antibody drug conjugates </li>
</ul>
<ul>
<li>Excellent problem-solving, critical thinking, and data analysis skills </li>
</ul>
<ul>
<li>Ability to work independently and as part of a collaborative team in a fast-paced and dynamic research environment </li>
</ul>
<ul>
<li>Strong track record of research accomplishments, as evidenced by publications in scientific journals </li>
</ul>
#LI-Onsite
Diversity and Inclusion (1910's Promise) 
At 1910, we believe that a diverse, equitable, and inclusive workplace furthers relevance, resilience, and longevity. We encourage people from all backgrounds, ages, abilities, and experiences to apply. 1910 is proud to be an equal-opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If, due to a disability, you need an accommodation during any part of the interview process, please let your recruiter know. While 1910 supports visa sponsorship, sponsorship opportunities may be limited to certain roles and skills. 
Benefits and Perks 
<ul>
<li>Competitive compensation package </li>
<li>Above market benefits </li>
<li>Generous vacation and parental leave </li>
<li>Super cool team building activities </li>
<li>Great colleagues </li>
</ul>

Scientist I, Assay Development for Small Molecule & Antibody Discovery (Biochemistry / Cell Biology)

<h3>Job Description</h3>
Job DescriptionTitle: Research Associate - Protein Analytics Adimab is the leading technology provider for therapeutic antibody drug discovery, focusing solely on our partnerships without pursuing an internal product pipeline. Since 2009, we have partnered with over 100 pharmaceutical and biotechnology companies, generating more than 600 therapeutic programs, of which more than 70 have entered clinical trials.&nbsp; Role Overview We are seeking a highly motivated Research Associate who is interested in liquid chromatography mass spectrometry (LCMS) to join our Protein Analytics group. The candidate will work in a small team setting to support Adimab’s novel antibody discovery, maturation, and production platform. This role requires the ability to multi-task in a productive and fast-paced environment. Responsibilities
<ul>
<li>Perform LCMS-related assays to characterize therapeutic antibodies and investigate post-translational modifications</li>
<li>Operate and maintain multiple liquid chromatography instruments and mass spectrometers</li>
<li>Critically interpret data and troubleshoot experiments</li>
<li>Communicate complex results effectively to colleagues and partners</li>
<li>Other responsibilities may include, but are not limited to, characterization of antibody samples using other analytical technologies such as IEX, HIC, SEC, SDS-PAGE etc.</li>
<li>Work in partnership with colleagues inside and outside of Protein Analytics</li>
</ul>
 Needed upon hire
<ul>
<li>B.S. in analytical chemistry, biochemistry, or related fields with 0-2 years of experience</li>
<li>Background / knowledge of mass spectrometry is desired</li>
<li>Basic understanding of chromatographic techniques is a plus</li>
<li>Strong attention to detail and organization</li>
<li>Basic skills with computer software such as Excel</li>
<li>Adaptable in a fast-paced environment</li>
<li>Communicates effectively and openly with colleagues and supervisor</li>
</ul>
 Come join us! Our integrated antibody discovery and engineering platform provides unprecedented speed from antigen to purified, full-length human IgGs with exquisite specificity and biophysical behavior. We offer&nbsp;fundamental advantages by delivering diverse panels of antibodies that meet the most demanding standards for affinity, epitope specificity, species cross-reactivity, and developability. We enable our partners to rapidly expand their biologics pipelines through a broad spectrum of technology access arrangements. As a profitable privately-held biotech company, we take a long-term view on value creation and make substantial investments in technology development, research, and our people. We offer individually tailored compensation packages comprised of a competitive salary, meaningful equity, a 2:1 401(k) match, and comprehensive health care benefits. Located in New Hampshire’s beautiful Upper Connecticut River Valley, we are minutes from Dartmouth College, the Geisel School of Medicine, the Thayer School of Engineering, the Tuck School of Business, and the Dartmouth Hitchcock Medical Center. We are fortunate to be situated in an area that is renowned for its premier skiing, hiking, kayaking, and biking.
Powered by JazzHR
KBd3pevfuI

Research Associate - Protein Analytics

<h3>Job Description</h3>
Job Description
About KalVista Pharmaceuticals, Inc.
KalVista Pharmaceuticals, Inc., is a global biopharmaceutical company dedicated to developing and delivering life-changing oral therapies for individuals affected by rare diseases with significant unmet needs. Our lead investigational product is sebetralstat, a novel, oral, on-demand treatment for hereditary angioedema (HAE). Sebetralstat is under regulatory review by the U.S. FDA, with a PDUFA goal date of June 17, 2025. In addition, we have completed Marketing Authorization Applications for sebetralstat to the European Medicines Agency and multiple other global regulatory authorities.
For more information about KalVista, please visit <a href="http://www.kalvista.com" target="_blank">www.kalvista.com</a> or follow us on social media at @KalVista and LinkedIn.
About Sebetralstat
Sebetralstat is an investigational, novel oral plasma kallikrein inhibitor for the treatment of hereditary angioedema (HAE). We have filed multiple regulatory applications seeking approval of sebetralstat as the first oral, on-demand treatment for HAE in individuals aged 12 and older, with ongoing studies exploring its use in children aged 2 to 11. If approved, sebetralstat has the potential to become the foundational therapy for HAE management worldwide.
 
About the Role:
KalVista seeks a dynamic and experienced Director, Global Evidence &amp; Outcomes Research to support global evidence generation strategy and lead planning and execution of patient-centered evidence generation activities supporting the launch and lifecycle management of clinical-stage assets within the Hereditary Angioedema (HAE) portfolio. 
Reporting to the Executive Director, Global Medical Affairs Lead, you will play a pivotal role in ensuring the generation of robust, actionable data that supports global medical affairs strategy execution as well as global regulatory and market access efforts. Collaborating closely with internal stakeholders across Medical Affairs, Market Access/HEOR, Commercial and R&amp;D teams, this role involves extensive external collaboration with HCPs, Healthcare Organizations (HCOs), Patient Advocacy Groups (PAGs) and Medical Societies. You will also oversee large-scale external expert advisory boards and consensus-like meetings, related to the evidence generation projects.
Management.
Responsibilities:
<ul>
<li>Support creation of a cross-functional and fully integrated evidence generation plan (IEGP)</li>
<li>Lead the development &amp; execution of evidence generation strategies and projects that address unmet clinical and patient-centered needs, supporting product value demonstration to regulators, healthcare providers, and patients</li>
<li>Provide outcomes research leadership, in alignment with HEOR and including the implementation of patient-reported outcomes (PROs) and health-related quality of life (HRQoL) measures, from late-stage clinical development through product commercialization</li>
<li>Design and oversee the execution of observational and epidemiologic research studies, ensuring timely and effective communication of results to key internal and external stakeholders</li>
<li>Manage and support generation of real-world evidence (RWE) within global expanded access programs (e.g., post-trial access, compassionate use), contributing to scientific publications and HTA submissions</li>
<li>Coordinate cross-functional collaboration with Patient Advocacy, Market Access, Marketing, Business Analytics, Development and Regulatory Affairs, ensuring alignment of evidence generation efforts to support value demonstration</li>
<li>Plan and lead large-scale external expert advisory boards and consensus-type meetings, ensuring input from key opinion leaders (KOLs), clinical experts, and patient representatives to inform the IEGP strategy</li>
<li>Support design of global evidence generation plans, ensuring they address the full product lifecycle including post-launch</li>
<li>Lead the design, execution, and analysis of prospective and retrospective observational studies, including longitudinal studies assessing patient outcomes, treatment patterns, comparative effectiveness, drug utilization and disease burden</li>
<li>Lead and manage investigator-initiated studies (IIS), ensuring scientific rigor, compliance, and alignment with company objectives</li>
<li>Oversee the execution of interventional studies, including Phase 3b and 4 studies if applicable, contributing to the understanding of long-term clinical outcomes and real-world use of the asset</li>
<li>Lead implementation of patient-reported outcome (PRO) and health-related quality of life (HRQoL) instruments tailored to the HAE patient population across evidence generation projects</li>
<li>Design and oversee patient and healthcare provider (HCP) surveys to gather insights on patient outcomes, disease burden and treatment patterns within the HAE space</li>
<li>Utilize claims data analyses and medical chart studies to generate valuable evidence on disease epidemiology, treatment patterns, and real-world outcomes</li>
<li>Oversee generation of real-world evidence (RWE) within global expanded access programs (e.g., post-trial access, compassionate use), to support the medical affairs and commercial strategy</li>
<li>Act as the medical lead for evidence generation related external engagements, including advisory boards, meetings with HCOs, PAGs and relevant regulatory bodies</li>
<li>Ensure alignment with internal stakeholders on evidence needs to support the global value dossier and reimbursement submissions</li>
<li>Prepare and review scientific publications, research protocols, statistical analysis plans (SAPs) and technical reports, communicating findings to both internal and external audiences</li>
<li>Serve as a key resource and thought leader for outcomes research strategy and evidence generation across the HAE portfolio</li>
</ul>
 
Qualifications:
<ul>
<li>Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant field such as health services research, health outcomes research, epidemiology, pharmacoeconomics or related disciplines</li>
<li>At least 8-10 years of experience in outcomes research or medical affairs with significant experience in the design, execution and management of global evidence generation activities in the life sciences industry</li>
<li>Proven track record of leadership in designing and executing patient-centered evidence generation strategies across the full lifecycle of clinical-stage assets</li>
<li>Expertise in the development of patient-reported outcomes (PROs) and health-related quality of life (HRQoL) assessments, with demonstrated success in applying these tools to clinical and market access strategies</li>
<li>Significant experience in designing, managing, and overseeing investigator-initiated studies (IIS), interventional studies, Phase 3b/4 trials, and real-world evidence generation (e.g., claims data analyses, medical chart studies)</li>
<li>Strong experience managing large-scale external expert advisory boards, consensus-type meetings, and interactions with regulatory authorities and other key stakeholders</li>
<li>Strong organizational and project management skills, with the ability to manage multiple priorities, timelines, and cross-functional teams in a matrixed multicultural global environment</li>
<li>Proven ability to work collaboratively across departments and regions, fostering a culture of cross-functional partnership and driving evidence generation that supports both medical affairs and commercial objectives</li>
<li>Exceptional communication skills with experience in preparing high-impact scientific documents, presenting to senior leadership and external experts and publishing peer-reviewed outcomes research</li>
<li>Extensive experience collaborating with external vendors, Healthcare Organizations (HCOs), Patient Advocacy Groups (PAGs), and Medical Societies to drive evidence generation efforts</li>
<li>A demonstrated record of global, cross-functional team leadership and a deep understanding of the regulatory, clinical, and commercial environments in pharmaceutical development</li>
<li>Experience in outcomes research specific to rare diseases or complex patient populations such as HAE preferred</li>
<li>A track record of successful peer-reviewed publications in outcomes research or related fields</li>
<li>Demonstrated success in leading global, cross-functional teams in a matrixed organization, ideally within the context of late-stage clinical development and commercialization preferred</li>
</ul>
 
KalVista is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
Important Notice to Third-Party Recruiters &amp; Staffing Agencies:
The current job openings advertised on this website are for the sole purpose of candidates to apply directly. Unsolicited and anonymous CVs submitted in any manner to KalVista employees, including to employee personal e-mail accounts, are considered to be the property of KalVista and will not qualify for a fee to be paid. Referral fees will only be payable where KalVista has agreed with an agency to work on a specific appointment, and then only in conjunction with a fully executed contract for service.
If any Agency representative contacts a KalVista Hiring Manager or company employee, other than a member of the KalVista Talent Acquisition team, to solicit an appointment to engage on a job opening, that Agency will not be considered for that specific job opening or future opportunities with KalVista.
Thank you for your understanding and cooperation.

Director, Global Evidence & Outcomes Research

<h3>Job Description</h3>
Job Description
Title: Research Associate - Sequencing Adimab is the leading technology provider for therapeutic antibody drug discovery, focusing solely on our partnerships without pursuing an internal product pipeline. Since 2009, we have partnered with over 100 pharmaceutical and biotechnology companies, generating more than 600 therapeutic programs, of which more than 70 have entered clinical trials.&nbsp;
Role We are seeking a skilled molecular biologist to join our team. This position will support Adimab's novel antibody discovery, maturation, and production platform by contributing to the sequencing core, performing core laboratory services, and taking on other responsibilities that may arise at a growing biotech company.&nbsp;
Responsibilities&nbsp;
<ul>
<li>Manage and perform work for the Adimab sequencing service&nbsp;</li>
<li>Operate and maintain sequencing and PCR instruments&nbsp;</li>
<li>Run automation equipment according to standard protocols&nbsp;</li>
<li>Assist with purchasing and maintenance of laboratory supplies and equipment&nbsp;</li>
<li>Troubleshoot and calibrate instruments&nbsp;</li>
<li>Prepare reagents, buffers, and media&nbsp;</li>
<li>Assist in preparation of samples for NGS runs&nbsp;</li>
</ul>
Needed upon hire&nbsp;
<ul>
<li>B.S. in molecular biology, biochemistry, or a related field&nbsp;</li>
<li>Prior laboratory experience&nbsp;</li>
<li>Familiarity with PCR and Sanger sequencing technology&nbsp;</li>
<li>Basic experience in molecular biology techniques&nbsp;</li>
<li>Demonstrated ability to work within defined standard operating procedures&nbsp;</li>
<li>Experience using Excel and knowledge of basic chemical calculations&nbsp;</li>
<li>Comfortable and productive in a fast-paced environment of ambiguity and change&nbsp;</li>
<li>Detail-oriented and highly organized&nbsp;</li>
<li>Strong time-management skills and ability to multi-task&nbsp;</li>
<li>Self-motivated and highly driven&nbsp;</li>
<li>Strong customer service and communication skills&nbsp;</li>
<li>An excellent team player, who also is able to work independently when appropriate&nbsp;</li>
</ul>
 Come join us! Our integrated antibody discovery and engineering platform provides unprecedented speed from antigen to purified, full-length human IgGs with exquisite specificity and biophysical behavior. We offer&nbsp;fundamental advantages by delivering diverse panels of antibodies that meet the most demanding standards for affinity, epitope specificity, species cross-reactivity, and developability. We enable our partners to rapidly expand their biologics pipelines through a broad spectrum of technology access arrangements.
As a profitable privately-held biotech company, we take a long-term view on value creation and make substantial investments in technology development, research, and our people. We offer individually tailored compensation packages comprised of a competitive salary, meaningful equity, a 2:1 401(k) match, and comprehensive health care benefits.
Located in New Hampshire’s beautiful Upper Connecticut River Valley, we are minutes from Dartmouth College, the Geisel School of Medicine, the Thayer School of Engineering, the Tuck School of Business, and the Dartmouth Hitchcock Medical Center. We are fortunate to be situated in an area that is renowned for its premier skiing, hiking, kayaking, and biking.
Powered by JazzHR
LUYbVJabhy

Research Associate - Sequencing

<h3>Job Description</h3>
Job Description
Company Overview 
1910 Genetics is a Series A stage biotechnology company that is pioneering a novel Input-Transform-Output (ITO™) platform as the first ever horizontal AI infrastructure for drug discovery. 
In a crowded space with hundreds of AI drug discovery companies, 1910's ITO™ platform is differentiated by: 
<ul>
<li>Modality agnostic drug discovery: our platform is capable of designing both small molecule and large molecule therapeutics across all disease areas, with an initial focus on neuroscience, oncology, and autoimmune diseases.</li>
<li>Proprietary massive multimodal data, which overcomes the data scarcity problem that prevents frontier AI models from being utilized for drug discovery.</li>
<li>Multi-AI agent systems that include a robust collection of frontier AI/ML models, each of which works in a task-oriented manner to achieve the multi-parameter optimization problem of drug discovery and development.</li>
<li>A state-of-the-art (SOTA) fully-automated, high throughput wet laboratory in the premier Boston Seaport District for both data generation for AI model training as well as validation of the safety and efficacy of drug candidates that are outputted by our frontier AI models.</li>
<li>An unprecedented partnership with Microsoft, which positions 1910 as the only biotech/pharma company leveraging Azure Quantum Elements, a groundbreaking, AI-driven, high performance computing (HPC) cloud architecture for advanced AI.</li>
<li>Bespoke conversational AI chatbots that provide a customer friendly UI/UX to access our platform for specific drug discovery tasks.</li>
<li>Being the only biotech company helping pharma companies integrate 6 core areas of AI infrastructure.</li>
</ul>
1910 Genetics is looking for an In Vitro Pharmacology Assay Scientist to work closely with our biologists in the discovery of antibodies. An expert in biochemical characterization of biological drug molecules, the ideal candidate will have experience in antibody drug discovery and characterization of a variety of molecular types. 
Role Responsibilities 
<ul>
<li>Validate target material in functional biochemical assays prior to the start of antibody discovery. </li>
</ul>
<ul>
<li>Design, validate and execute in vitro biochemical assays for the screening of molecules from 1910 Genetics' AI-driven large molecule therapeutics platform </li>
</ul>
<ul>
<li>Develop, validate and execute assays for the biophysical characterization of antibodies in various formats and for various modalities </li>
</ul>
<ul>
<li>Work closely with 1910 scientists to refine assays to help drive delivery of program objectives </li>
</ul>
<ul>
<li>Maintain detailed records of experimental procedures and results in electronic lab notebook </li>
</ul>
<ul>
<li>Present experimental results/progress in a timely manner and contribute to scientific discussion in group meetings </li>
</ul>
<ul>
<li>Collaborate with cross-functional teams, including AI Research and Computational Chemistry to discuss project updates as well as ensure the project milestones and timelines are met </li>
</ul>
<ul>
<li>Assist laboratory operations, including maintenance of equipment, reagent tracking and monthly inspections for safety equipment </li>
</ul>
<ul>
<li>Develop and execute standard operating procedures and best practices to enhance lab efficiency and productivity </li>
</ul>
<ul>
<li>Contribute to the preparation of scientific reports, presentations, and publications. </li>
</ul>
<ul>
<li>Provide intellectual input into small molecule projects when required </li>
</ul>
<ul>
<li>Stay current with scientific literature and emerging technologies in the fields of large and small molecule research </li>
</ul>
#LI-Onsite
Qualifications 
<ul>
<li>PhD in Biology with a focus on Biochemistry, Cell Biology, In Vitro Pharmacology, Biomedical Sciences or a related field </li>
</ul>
<ul>
<li>Postdoctoral experience or relevant industry experience in drug discovery or In Vitro Pharmacology </li>
</ul>
<ul>
<li>Experience in developing, validating and implementing biology, biochemical, and cell-based assays </li>
</ul>
<ul>
<li>Familiarity with signal transduction pathways in relevant therapeutic areas such as Immunology &amp; Inflammation, neuroscience, oncology, and cardiometabolic diseases </li>
</ul>
<ul>
<li>Experience with immune cell isolation and assay development </li>
</ul>
<ul>
<li>Experience using analytical techniques/instrumentation for characterization and quantification of large molecules, including chromatographic techniques such as HIC (Hydrophobic Interaction Chromatography) and RP (Reverse Phase), SEC (Size Exclusion Chromatography), SDS-PAGE, UV-Vis, etc. </li>
</ul>
<ul>
<li>Familiarity with conjugation, purification and characterization of antibody drug conjugates </li>
</ul>
<ul>
<li>Excellent problem-solving, critical thinking, and data analysis skills </li>
</ul>
<ul>
<li>Ability to work independently and as part of a collaborative team in a fast-paced and dynamic research environment </li>
</ul>
<ul>
<li>Strong track record of research accomplishments, as evidenced by publications in scientific journals </li>
</ul>
Diversity and Inclusion (1910's Promise) 
At 1910, we believe that a diverse, equitable, and inclusive workplace furthers relevance, resilience, and longevity. We encourage people from all backgrounds, ages, abilities, and experiences to apply. 1910 is proud to be an equal-opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status. If, due to a disability, you need an accommodation during any part of the interview process, please let your recruiter know. While 1910 supports visa sponsorship, sponsorship opportunities may be limited to certain roles and skills. 
Benefits and Perks 
<ul>
<li>Competitive compensation package </li>
<li>Above market benefits </li>
<li>Generous vacation and parental leave </li>
<li>Super cool team building activities </li>
<li>Great colleagues </li>
</ul>

190 Science Jobs