JOB TITLE:&nbsp; Senior Clinical Trial Specialist DEPARTMENT:&nbsp; Clinical Operations HIRING MANAGER:&nbsp; Lorna Dean LOCATION:&nbsp; South San Francisco, California / Remote (Hybrid) TYPE:&nbsp; Full-TimeHI-Bio is a clinical-stage biotechnology company based in South San Francisco, California.&nbsp;Our shared purpose is to transform the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. We have a precision medicine approach grounded in emerging human genetics.&nbsp;HI-Bio's team is made up of industry experts from science and technology.&nbsp;We are on a path to building the leading immunology company.&nbsp;To accomplish this, we are seeking top talent to join us on our journey.We are seeking a Senior Clinical Trial Specialist to assist in the execution of Clinical Trials.&nbsp;The successful candidate will be able to support the conduct of clinical trials with minimal guidance/supervision while ensuring alignment with GCP and HI-Bio’s SOPs. The Specialist&nbsp;provides a high level of administration, coordination and organizational support to the Clinical Study Lead and team members from all functions involved in assigned study(ies). The role requires an ability to manage multiple priorities consecutively and priorities consecutively and sequentially and meeting quality standards for accuracy, attention to detail and timelines. As part of a growing clinical development operations team, the Specialist will help define various aspects of clinical trials to ensure timely completion, efficient protocols, budget alignment, and compliance with ICH/GCP Guidelines.The role reports to the Senior Vice President, Development operations. Level will be commensurate with experience.KEY RESPONSIBILITIES:<ul style="list-style-type:disc;"><li>Overall global tracking of study deliverables with escalation of key issues/trends.</li><li>Support and/or manage protocol related site/supplier activities.</li><li>Assist and/or manage in the design, format, review and content of study guides, worksheets, quick reference cards and other materials/documents used to support the study.</li><li>Contribute to protocol review and amendment management, including informed consent initiation and updates.</li><li>Attend, contribute and potentially lead supplier meetings; work with suppliers to resolve issues, and foster process improvements.</li><li>Monitor progress of studies, help identify study related trends/issues and work with Clinical Trial Managers (CTM) to implement corrective actions when necessary.</li><li>Submission of documents to TMF and assist with TMF reconciliation as needed.</li><li>Oversee study start-up activity tracking with CTM oversight.</li><li>Assist with maintaining FAQ and ADI logs; manage resolution of actions.</li><li>May assist with the quality control of clinical data for CSR preparation.</li><li>Assist CTM with meeting agenda and maintain minutes for internal /external team meetings.</li><li>Assist tracking study milestones in tools and dashboards.</li><li>Point of contact (as delegated) for study related issues.</li><li>May participate in data review (e.g., line listings).</li><li>Contribute to the development of recruitment strategies and materials; assist with external recruitment activities and supplier management.</li><li>Work with sample management to coordinate shipment and analysis of sample needs; lead reconciliation efforts.</li><li>Track study level investigational product accountability and reconciliation for studies and at close-out with depots; align with CMC to determine supply needs.</li><li>Manage temperature excursion process flow.</li><li>Help coordinate investigator meetings, study related workshops, and other meetings as applicable.</li><li>May provide clinical site support (e.g., materials to site/CRAs).</li><li>Support and contribute to Inspection Readiness processes.</li><li>May participate in cross-functional study management activities and&nbsp;process improvement initiatives.</li><li>Postings to clinical trial websites.</li><li>Lead Site Management Oversight tasks to ensure CRO activities are being completed per the Monitoring Plan.</li><li>May conduct monitoring/co-monitoring visits with CRO or CTM.</li><li>Participate in User Acceptance Testing (UAT) with supplier systems.</li><li>Contribute to protocol review, content and ICF development.</li><li>Overall collaboration with process development and implementation.</li><li>Some travel may be required (&lt;30%).</li></ul>EDUCATION AND QUALIFICATIONS:<ul><li>Combination of degree and relevant Biopharma related experience within a pharmaceutical, biotech environment or other relevant experience.<ul style="list-style-type:circle;"><li>Bachelor’s degree and 3 years of direct related experience or</li><li>Associates degree and 5 years of direct related experience or</li><li>High school diploma or equivalent and 6 years of direct related experience and</li><li>3 years direct experience in a Clinical Operations related function/role</li></ul></li><li>Ability to manage multiple priorities and allocate tasks efficiently to keep trials on track</li><li>Experience in a small company or immunology is a plus</li><li>Current knowledge of ICH, GCP, and other regulatory guidelines</li><li>Ability to think critically and solve problems, possesses a quick and analytical mind, is a fast‑learner and works well in an organization that places a high value on intellectual capacity</li><li>Strong attention to detail and an ability to identify gaps and innovate solutions</li><li>Excellent written and verbal communication and a highly motivated disposition&nbsp;</li></ul>HI-BIO RECRUITING: HI-Bio, Inc. is an equal opportunity employer. We value diversity and do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We are committed to creating an inclusive environment for all employees.

Clinical Operations

Senior Clinical Trial Specialist

JOB TITLE:&nbsp; Manager/Senior Manager, Clinical Development Operations Optimization DEPARTMENT:&nbsp; Development Operations HIRING MANAGER:&nbsp; Lorna Dean LOCATION:&nbsp; South San Francisco, California / Remote TYPE:&nbsp; Full-Time&nbsp;HI-Bio is a clinical-stage biotechnology company based in South San Francisco, California.&nbsp;Our shared purpose is to transform the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster.&nbsp;We have a precision medicine approach grounded in emerging human genetics.&nbsp;HI-Bio's team is made up of industry experts from science and technology.&nbsp;We are on a path to building the leading immunology company.&nbsp;To accomplish this, we are seeking top talent to join us on our journey.We are seeking a Manager/Senior Manager Development Operations Optimization to manage the execution of Clinical Trial related activities at HI-Bio.&nbsp; The successful candidate will be able to execute their duties with minimal guidance/supervision while ensuring alignment with GCP and HI-Bio’s SOPs. As our portfolio and programs mature and advance, this person will impact our ability to initiate, monitor, and organize clinical trials quickly and accurately. The role is highly collaboration focused and will work with other development teams to implement new tools, processes, and other solutions to address current and future challenges. Our ideal candidate will have ample experience in clinical development operations and will have a desire to oversee tactics and methods to improve clinical trial efficiency and accuracy.KEY RESPONSIBILITIES:<ul><li>Support and/or manage clinical study planning deliverables for a study or program, including milestone tracking, timelines and dashboards</li><li>Business process owner of trial master file (TMF) and all related processes and TMF study related activities.&nbsp; Oversight of TMF related staff/resources.</li><li>Manage supplier related activities for TMF and other suppliers within span on control</li><li>Monitor and track planning milestones of studies, help identify study related trends/issues and work with Clinical Study Team to gather and maintain current information.</li><li>Attend and contribute to supplier meetings, work with suppliers to resolve issues, and foster process improvements.</li><li>Design and manage training material, Quick Reference and&nbsp; FAQ logs for areas of responsibility.</li><li>Develop and manage controlled documentation supporting areas of responsibility.&nbsp;</li><li>Participate on the clinical study teams&nbsp;</li><li>Support and contribute to Inspection Readiness processes.&nbsp;</li><li>May participate in cross-functional process improvement initiatives.</li><li>May lead and/or participate in User Acceptance Testing (UAT) with supplier systems.</li><li>Contribute to various clinical operations and development operations process deliverables.</li></ul>EDUCATION AND QUALIFICATIONS:<ul style="list-style-type:disc;"><li>Combination of degree and relevant Biopharma related experience within a pharmaceutical, biotech environment or other relevant experience.<ul style="list-style-type:circle;"><li>Doctorate degree and 2 years of direct related experience or</li><li>Master’s degree and 6 years of direct related experience or</li><li>Bachelor’s degree and 8 years of direct related experience and</li><li>2 years direct experience in a Development Operations related function/role</li></ul></li><li>Demonstrated experience in successfully managing study timelines, vendors, and other tracking.</li><li>High attention to detail and an ability to find potential gaps and implement solutions.</li><li>Experience in immunology is a plus; experience in a lean, small company is a plus.</li><li>Strong written and verbal communication.</li><li>Current and abreast knowledge of emerging trends, systems, processes, and regulatory requirements as it relates to clinical trial administration.</li><li>Experience designing training materials, SOPs, and new process initiatives is highly desired.</li><li>Ability to adapt and work in a fast-paced environment.</li><li>A “can-do” disposition and an innate desire to refine activities.</li><li>Ability to travel up to 30%, which may vary on study and other timelines.</li></ul>HI-BIO RECRUITING: HI-Bio, Inc. is an equal opportunity employer. We value diversity and do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We are committed to creating an inclusive environment for all employees.

Development Operations

Manager/Senior Manager, Clinical Development Operations Optimization

JOB TITLE: Director, Clinical ScienceDEPARTMENT: Clinical DevelopmentLOCATION: South San Francisco, CaliforniaTYPE:&nbsp; Full-Time (Onsite / Hybrid)Are you an experienced scientist with clinical research experience in kidney and/or immune-mediated diseases? Join HI-Bio, Inc. a clinical-stage biotechnology company based in South San Francisco, California, and be part of a fast-paced organization on an outstanding team of cross functional clinical research professionals translating scientific insights into our clinical development programs across a wide range of unmet needs.&nbsp; Our shared purpose is to transform the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact. We have a precision medicine approach akin to oncology and grounded in human genetics. Our pipeline is strong and built through in-licensing and discovery. HI-Bio's team is made up of industry experts from science and clinical development. We are on a path to building the leading immunology company. To accomplish this, we are seeking top talent to join us on our journey.We are seeking&nbsp;a senior Clinical Scientist to support clinical research activities for our portfolio our immunology clinical programs, with a specific emphasis on severe immune-mediated diseases. This position provides leadership in program development, execution, innovation, and optimization of clinical trials by including the latest insights on disease mechanisms, diagnostic approaches, and alternative therapies. The Director will primarily be involved in activities associated with the design, execution, monitoring, data interpretation, and reporting of clinical studies evaluating novel therapies across target indications. Additional responsibilities involve assisting with regulatory documentation by &nbsp;collaborating with discovery, development, and commercial colleagues, as well as managing external collaborations and gaining comprehensive knowledge of the literature related to the product(s) in development. The responsibilities of this role may vary depending on the specific indication and trial requirements.The Clinical Scientist collaborates closely with Study Physicians/Scientists as a key member of development and core team. The role actively contributes scientific expertise to cross-functional clinical teams involved in the development of novel therapies. As part of a startup environment, the role involves extensive matrix interactions with colleagues from various disciplines to ensure the successful execution of clinical development plans and regulatory filings. Our ideal candidate will have significant experience in clinical trials for antibodies and can strongly communicate and present relevant clinical data to leadership and core teams.KEY RESPONSIBILITIES:<ul style="list-style-type:disc;"><li>Support the preparation of clinical development plans, trial protocols, case report forms, and study operational plans that are scientifically rigorous, clinically relevant, operationally feasible, while adhering to GCP and regulatory requirements</li><li>Establish and maintain credible relationships with clinical investigators and medical/scientific experts</li><li>Collaborate with Clinical Operations in trial setup, conduct, recruitment activities, closeout, and reporting</li><li>Assist Data Management with the review of clinical data and resolution of queries</li><li>Perform medical monitoring activities and reporting in partnership with Study Responsible Physicians/Scientists, including evaluating clinical trial adverse events and reviewing clinical laboratory results</li><li>Work closely with Quality Management &amp; Assurance to ensure flawless execution of clinical trials</li><li>Draft and coordinate completion of clinical study reports</li><li>Prepare responses to questions from Ethics Committees and Health Authorities</li><li>Support integrated document development for marketing authorization filing</li><li>Interpret, report, and prepare oral and written results of product research, in collaboration with senior clinical personnel, in preparation for health authority submissions</li><li>Support preparation for FDA Advisory Committee and EU Oral Explanation</li><li>Present relevant clinical data to internal and external stakeholders</li><li>Review medical literature and related new technologies relevant to the assigned projects.</li><li>Other responsibilities may include utilizing nonclinical PK and PK/PD data (including use of modeling and simulation techniques) to project optimal clinical dosing regimens, doses based on pharmacological/clinical targets, human starting doses, and biomarker exploratory data (including biochemical and molecular data from quantification of mRNA, multi-panel flow cytometry, and protein expression)</li><li>Collaborate with early research teams in assessing PK and other data for use in future programs and to optimize experimental design</li><li>Author regulatory documents as it relates to clinical pharmacology data and design</li><li>Evaluate and implement necessary tools and systems to organize and analyze data</li><li>Conduct clinical studies with utmost integrity, professionalism, and organization&nbsp;</li></ul>QUALIFICATIONS:<ul style="list-style-type:disc;"><li>PhD/PharmD with 5+ years of industry clinical research experience, preferably in immunology or a related therapeutic area. BS/MS/RN will be considered with additional industry and drug development experience</li><li>Experience in late-stage drug development, with a preference for experience in immuno-inflammatory indications</li><li>Strong analytical skills coupled with communication skills to present findings and relevant data</li><li>Ability to survey and interpret scientific literature related to assigned projects</li><li>Strong organizational skills and ability to thrive in a fast-paced startup environment while prioritizing and responding to changing business needs</li><li>Demonstrated ability to collaborate effectively with cross functional teams and champion and drive solutions for clinical challenges</li><li>Excellent written and verbal English communication skills</li><li>Ability to interface with health authorities and represent clinical programs with integrity, polish, and professionalism&nbsp;</li><li>Ability to travel domestically and internationally, approximately 10-20% of the time.</li></ul>HIBIO RECRUITING:HI-Bio, Inc. is an equal opportunity employer. We value diversity and do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We are committed to creating an inclusive environment for all employees. HI-Bio Inc. does not accept unsolicited resumes from any agency that we have not directly engaged on a specific role. Our managers and employees will not accept resumes sent directly from any agency/3rd party. Unsolicited resumes sent to HI-Bio, Inc. from recruiters do not constitute any type of relationship between the recruiter and/or recruiting agency and HI-Bio, Inc. and do not obligate HI-Bio, Inc. to pay fees should we hire from those resumes.&nbsp;

Clinical Development

Director, Clinical Science

JOB TITLE:&nbsp;&nbsp;Senior Director, Regulatory AffairsDEPARTMENT:&nbsp;Regulatory AffairsLocation:&nbsp; South San Francisco, CA&nbsp;(Onsite / Hybrid)TYPE: Full-TimeHI-Bio, Inc. is a clinical-stage biotechnology company based in South San Francisco, California. Our shared purpose is to transform the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. Our pipeline is strong and built through both in-licensing and discovery. HI-Bio's team is made up of industry experts from science and clinical drug development. We are on a path to building a leading immunology company. To accomplish this, we are seeking top talent to join us on our journey.Reporting to the Senior Vice President, Regulatory Affairs, the Senior Director, Regulatory Affairs is responsible for the development and implementation of our global regulatory strategy. This role will provide regulatory leadership at a program level and requires in depth experience leading regulatory strategy and an innate ability to adapt and move quickly in a startup environment. Our ideal candidate will have experience in the immunology space and expertise in global regulatory filings.&nbsp;KEY RESPONSIBILITIES:<ul style="list-style-type:disc;"><li>Leads the design and implementation of regulatory strategies for assigned development programs, providing strategic guidance and leadership to project teams on all regulatory matters</li><li>Collaborate with team members, management, and consultants to define regulatory pathways at a global level&nbsp;</li><li>Oversee the preparation, submission, and management of regulatory submissions (e.g., INDs, CTAs, BLAs, MAAs), ensuring compliance with applicable regulations and guidelines</li><li>Establish and maintain effective relationships with the FDA and other relevant regulatory agencies; serve as the primary point of contact for assigned programs</li><li>Plan, implement, and lead effective interactions with regulatory authorities, including FDA, EMA, and other global health authorities, to facilitate successful regulatory submissions and approvals</li><li>Proactively identify regulatory risks and develop mitigation strategies&nbsp;</li><li>Ensure compliance with relevant regulatory requirements, company policies, and industry standards, maintaining the highest standards of ethical conduct and integrity</li><li>Contribute to the project team by developing or overseeing the overall content and timing of regulatory filings, consistent with applicable regulations, guidelines, and standards</li><li>Remain current with evolving regulatory requirements, guidelines, and competitive landscape to inform regulatory strategy and decision-making</li><li>Support the regulatory aspects of new or ongoing clinical trials, including during study start up, study conduct, and study completion</li><li>Author documents for regulatory filings as needed; work with other team members to define the outline and content of documents for regulatory filings</li><li>Represent the company externally in regulatory matters, including participation in industry forums, conferences, and regulatory agency meetings</li><li>Manage or direct the management of timelines to ensure regulatory filings occur on time</li><li>Identify and assess regulatory risks and risks to timelines for assigned projects or programs</li><li>Monitor and review regulatory agency communications such as changes to regulations and guidelines, and summarize these for team members, as appropriate</li><li>Ensure internal regulatory compliance by developing effective departmental procedures, including development and review of SOPs</li><li>Work to influence external regulatory environment through active participation in conferences and industry/agency regulatory meetings, committees and trade associations</li><li>Champion our culture through living our values and mentoring junior colleagues&nbsp;</li></ul>EDUCATION AND QUALIFICATIONS:<ul style="list-style-type:disc;"><li>Advanced degree in life sciences, pharmacy, or related field; PhD or PharmD preferred; experience in immunology is a plus</li><li>15+ years of industry regulatory experience with roles of increasing responsibility</li><li>Broad regulatory experience across multiple therapeutic areas, geographical regions (US, Canada, EU, Japan) and therapeutic modalities</li><li>Experience with all aspects of the regulatory process including strategy (agency interactions, application planning) and operations (meeting request, background packages, IND through NDA/BLA submissions)</li><li>Strong leadership and communication skills, with the ability to influence and collaborate effectively across functions and levels of the organization</li><li>Energetic, creative, analytical problem solver who acts independently yet communicates broadly so that appropriate business decisions can be made</li><li>Strategic thinker with the ability to anticipate and mitigate regulatory risks</li><li>Knowledge of current and changing regulatory landscape and guidelines for BLAs and other therapeutic programs</li><li>Excellent oral and written communication skills</li><li>Ability to collaborate and influence across all levels of the organization</li><li>Demonstrated ability to thrive in a fast-paced, entrepreneurial environment</li></ul>HI-BIO RECRUITING: HI-Bio, Inc. is an equal opportunity employer. We value diversity and do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We are committed to creating an inclusive environment for all employees.

Regulatory Affairs

Senior Director, Regulatory Affairs

JOB TITLE:&nbsp;&nbsp;Director, Medical WritingDEPARTMENT:&nbsp;Regulatory AffairsLOCATION:&nbsp;South San Francisco&nbsp;(Onsite/Hybrid)TYPE: Full-TimeHI-Bio, Inc. is a clinical-stage biotechnology company based in South San Francisco, California. Our shared purpose is to transform the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. Our pipeline is strong and built through both in-licensing and discovery. HI-Bio's team is made up of industry experts from science and clinical drug development. We are on a path to building a leading immunology company. To accomplish this, we are seeking top talent to join us on our journey.This role is responsible for the planning, coordination, and oversight of all medical writing activities within the company.&nbsp;In this role you will lead the Medical Writing function and be responsible for the development and implementation of a standardized process for the development of clinical and regulatory documents and will be responsible for managing external resources. This position will report into the Senior Vice President, Regulatory Affairs.KEY RESPONSIBILITIES:<ul style="list-style-type:disc;"><li>Responsible for planning, managing, and aligning medical writing activities and communication across multiple projects and development programs&nbsp;</li><li>Oversee the development of critical documents, including Investigator Brochures, protocols/protocol amendments, and clinical study reports, in compliance with SOPs, ICH E3 guidelines, other applicable regulatory guidance documents, and local requirements</li><li>Support the selection of CROs and vendors and provide project-level oversight of CROs and other vendors</li><li>Develop the medical writing functional area, including creation of standardized policies, procedures, work instructions, timelines, document tools and templates, style guide, and best practices&nbsp;</li><li>Responsible for clinical trial disclosure (CTD) and registration activities (e.g., CT.gov Registration/Results, EU CTR Results, Plain Language summaries, Redacted Clinical Documents). May be directly involved in activities related to CTD as well as providing oversight to vendor supporting these activities. Effectively engage and communicate with functional area leads and stakeholders across development programs to support medical writing and CTD activities.</li><li>Provides leadership in planning and contributing to key regulatory submissions to US and global health authorities (BLAs, MAAs, INDs, annual reports, DSURs).&nbsp;</li><li>Ensures key messages are clear and consistent within and across documents.</li><li>Contributes strategically and scientifically at the project and/or study team level.</li><li>Responsible for forecasting costs for individual medical writing projects</li><li>Generate and track medical writing project budgets against planned budget and timelines&nbsp;</li><li>Partner with legal and financial functions to negotiate medical writing contracts and budgets</li><li>Identify and anticipate issues related to budget and project milestones and lead mitigation and resolution efforts for issues identified</li><li>Create and regularly update medical writing project timelines and ensure that medical writing timelines are in sync with the program timelines</li><li>Act as a key contributor to the organization cross-functionally to promote organizational goals and knowledge sharing</li><li>Lead and drive process improvement initiatives for medical writing and CTD, including development and maintenance of standard operating procedures</li></ul>EDUCATION AND QUALIFICATIONS:<ul style="list-style-type:disc;"><li>Bachelor’s degree (life science preferred) combined with&nbsp;+10 years of pharmaceutical/biotechnology medical writing experience including development of regulatory documents for Phase I-III clinical trials</li><li>A Master’s (MS) or PhD degree may be considered in place of years of relevant experience</li><li>Subject matter expert in the regulatory medical writing process with strong attention to detail</li><li>Demonstrated ability to communicate and write clearly, concisely, and effectively. Aptitude for compilation, analysis, and presentation of data</li><li>Demonstrated experience in the preparation of protocols, study reports, investigator brochures, safety updates, and other clinical and regulatory documents required for IND and NDA submissions</li><li>Demonstrated experience in a lead medical writing role managing projects of varying size and complexity, preferably within a biotech company or contract research organization (CRO)</li><li>Experience managing medical writing vendors and/or contract medical writers</li><li>Excellent communication skills, written and oral, to ensure that medical writing plans and processes are transparent, strict timelines are met, and risks, issues, and results are clear to all stakeholders</li><li>Outstanding organizational skills with the ability to multi-task, prioritize, negotiate, manage competing priorities, analyze and solve problems</li><li>Thorough knowledge of regulatory and compliance requirements for medical writing, including ICH E3 and other applicable guidelines</li><li>Willing to embrace change and work in a changing environment</li><li>Able to work collaboratively across cultures and geographies</li><li>Proficient in Microsoft® Word, Project, PowerPoint, Excel&nbsp;</li><li>Proficient in Adobe Acrobat, and electronic document templates (e.g. eCTD templates)</li></ul>HI-BIO RECRUITING:HI-Bio, Inc. is an equal opportunity employer. We value diversity and do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We are committed to creating an inclusive environment for all employees.

Director, Medical Writing

Jobs

Join the HI-Bio™ team to improve the lives of patients with severe immune-mediated diseases (IMDs).

Senior Director, Alliance Management & Corporate Development

Senior Office Manager

Director, Biology & Project Team Lead

We develop extraordinary therapeutics with urgency

Patients are at the center of what we do. We are working towards developing and delivering medicines that will change a poor prognosis to a healing one. We all have a part to play in making that hope a reality, and there is no time to waste.

Deliver for patients

We seek to realize the full potential of our programs

We apply our knowledge, skills, and expertise to advance our programs into diseases where we have the best opportunity to provide outsized benefit for patients and their loved ones, our employees, shareholders and for society.

Optimize for impact

We focus on what matters

We are focused on achieving our mission, and the path to that is operational excellence. We have a high bar for the quality of our work. We are a tight-knit, focused team that deliberately removes distractions and executes towards our goals.

Execute deliberately

We collaborate as one team, and value diversity of thought and people

We are individually strong and capable, but we maximize our potential by collaborating as one team. People are our greatest asset, and we foster a workplace of belonging and equity. We actively seek different points of view and recognize the value of everyone's skills and contributions.

Be stronger, together

We do what is right, always

Integrity is the foundation of our business. We own our actions and do what's right, honest, and ethical. We lead by putting integrity first and considering our impact on others. Integrity begins with everyone at HI-Bio.

Lead with integrity

Our Values

We are currently accepting resumes. If you’re excited to realize the power of precision medicine, send us a note, and say ‘HI’.