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QA Manager
Company: Denali Therapeutics
Location: Salt Lake City, UT
Posted Nov 17, 2023
Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Committed to Denali values of growth, unity, grit and trust as well as values related to accountability, transparency, and scientific rigor. and approve as required Author and/or review documentation for product release including, inventory verifications, batch record review, investigations, change control, laboratory reports, validation protocols and reports, calibration documentation and batch summary reports Provide document reviews or input for quality or other external functions, in a constructive team-oriented manner with urgency and a continuous improvement perspective Clear, collaborative, and effective communication to discuss quality requirements with internal and external Denali partners including, manufacturing operations, MSAT, engineering, facilities, QC, warehouse, Corporate QA, and TechOps teams Additional activities assigned or required as directed Preferred Qualifications: At least 10 years in clinical cGMP pharmaceutical Quality Assurance. Eur./FDA/ISO/GMP standards and guidance Ability to effectively collaborate in a dynamic, fast paced, multidisciplinary team environment. Support implementation of Quality Management System (QMS) processes including change control, d Deviation, document control, and CAPA Execute and manage required change controls, deviation, document change and CAPA processes Document and report product or service-related quality events Support the development and implementation of standard operating procedures, policies and work instructions for processes governing quality services throughout the manufacturing facility and warehouse Support the development of raw material chemical and consumable standards for inspection Review data compilations (stability, batch analyses, environmental monitoring, etc.) Working knowledge of cGMP computer system solutions (MasterControl, LabWare LIMS, Netsuite preferred) Familiarity with large molecule drug substance manufacturing Knowledge of current USP/Ph. Primary Responsibilities and Essential Functions: Provide QA support to all site GMP Operations, including manufacturing, Quality Control and Warehouse Operation. Salary Range: $130,000.00 to $156,667.00.
Director, Biostatistics
Company: Dyne Therapeutics
Location: Waltham
Posted Nov 17, 2023
Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. DSURs, Briefing Documents, etc. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload. The ideal candidate must be a good communicator, exhibit high-energy, self-motivation, and forward‑thinking. LI-Onsite The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Primary responsibilities include: Serve as a biostatistics expert for assigned clinical studies or compound-level activities Effectively interact with members in other functions including medical, regulatory, safety, clinical operation, and translational medicine for strategic planning to ensure optimized clinical development in accordance with corporate objective Work collaboratively with internal and external (e.g., CRO) team members to coordinate the planning and execution of statistical deliverables Contribute to clinical protocol development, including authoring of the Statistics section and reviewing of other sections by applying statistical principles Design and specify stratification /randomization schema; review and approve test randomization lists Collaborate with Data Management, Clinical Development and Clinical Operations on design and review of eCRFs, and ensure data collection meet the requirements of statistical analyses Author or oversee the development of statistical analysis plans for clinical trials and for integrated summaries of safety/effectiveness (ISS/ISE), provide guidance to statistical programmers on SDTM/ADaM and oversee the development of shells for tables, figures and listings Provide statistical input to data monitoring committee (DMC) charters, independent review charters, and other study-level documents Validate the results of key statistical deliverables Contributes to clinical study reports and other regulatory documents e.g. Perform ad hoc and exploratory statistical analyses as needed Be accountable for assigned statistical activities in support of IND/NDA/MAA or other regulatory submissions Address statistical questions/comments from FDA and other regulatory agencies, and review and address comments by IRB/ECs Support and contribute to the preparation of publications, including manuscripts, posters and oral presentations Represent Dyne regarding statistical issues in meetings with external parties including regulatory agencies and corporate partners Identify and implement emerging new ways of doing clinical development and new methodologies Contribute or lead standardization and process improvement efforts for Biostatistics function and contribute to cross-functional process improvement efforts Education and Skill Requirements: Ph.D. in statistics or Biostatistics or equivalent with at least 8 years of experience in the pharmaceutical or biotech industry Interest in and basic understanding of biology and biological process including ASO and siRNA Demonstrated ability and experience in the design, analysis and reporting of clinical trials Experience in NDAs, MAAs or other regulatory submissions desirable In-depth knowledge of statistical methods for clinical trials, including both frequentist and Bayesian approaches Knowledge of FDA, EMA and ICH regulations and guidelines Proficient in statistical programming (SAS is required and R is a plus) Experience with trial design software (e.g., EAST) Ability to concurrently lead statistical efforts for multiple studies Understanding of data standards, including SDTM and ADaM Adept at overseeing statistical services provided by CRO’s and/or contractors Ability to work independently and act with initiative to address issues Ability to effectively communicate statistical concepts in a clear and concise manner both written and verbally. This person will be responsible for statistical activities including: designing innovative clinical trials, authoring statistical sections of protocols, preparing statistical analysis plans, ensuring quality in implementation of statistical analysis, interpreting and communicating the results of statistical analysis of clinical trial data in support of regulatory submissions as well as manuscripts, and leading biostatistics support for worldwide regulatory submissions. The employee may be requested to perform different or additional duties as assigned.
Associate Director, QC for QA, CMC Quality
Company: Denali Therapeutics
Location: Peninsula
Posted Nov 17, 2023
Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class. Responsibilities (include but are not limited to the following) Provide Analytical and QC Subject Matter Expertise within the Quality Group Oversee GMP Quality operations at CMOs, with a focus on QC activities, including quality documentation reviews and approvals and assisting the disposition of Denali products Support PPQ activities which will include review of process validation protocols/reports, risk assessments, method validation protocols and all associated reports Write Quality documentation including specifications, SOPs and Policies Support supplier qualification and quality audits for Denali sites including CMOs/CTLs as needed Oversee product quality aspects of the supply chain and distribution networks Establish and support quality systems and operations, including document control, change controls, deviation, CAPA, effectiveness checks and temperature excursions Improve quality processes and systems and seek continued improvement Support CMC development including review and approval of QC specific documentation including CofA’s, specifications, stability studies, method validation, test methods, process validation and all associated QC data Support efforts to implement and utilize the internal electronic document management system Support and review relevant sections of IND/IMPD/BLA/NDA Requirements Minimum of 7 years of QC GMP experience in the Biotech/Pharmaceutical industry BS degree in a scientific discipline is required and a post graduate degree is a plus Experience with CMOs, CMC development with focus on both large and small molecules Experience of releasing or supporting release of clinical or commercial drug substance & drug product Current and strong working knowledge of 21 CFR Parts 210-211 and 11; EU cGMP/GLPs; and ICH quality and development guidelines Current and strong working knowledge of Out of Specification (OOS) Investigations Driven, results-oriented self-starter and excellent team player Creative and pragmatic approach to problem solving and issue resolution Able to travel domestically and internationally Denali is committed to its core company value of unity by creating a diverse and inclusive environment. Applicant Privacy Policy https://www.denalitherapeutics.com/denali-applicant-privacy-policy LI-AS1 Salary Range: $162,000.00 to $192,333.00. This role will also contribute to establishing the growth and development of the Quality organization to include, developing quality processes and documentation, and supporting implementation of an Electronic Document Management System (EDMS) and quality modules. Learn more at https://www.denalitherapeutics.com/careers *This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future. The Associate Director QC for QA will report to the Executive Director, Quality and will provide Quality oversight of Denali’s external manufacturing and laboratory network (CMO/CLOs), support internal/external CMC development activities, release of clinical and commercial material and audits. Denali Therapeutics is dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degenerative biology and the principles of translational medicine.
Principal Biostatistician
Company: Denali Therapeutics
Location: Peninsula
Posted Nov 17, 2023
Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class. Highly independent, curious and creative, can do attitude, and embraces continuous improvement culture. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Familiarity with industry data standards, including CDISC, SDTM and ADaM data models. Strong programming skills in R, Shiny, Markdown; working knowledge of Git and Unix/Linux environments. Requirements PhD. Salary Range: $185,000 to $222,333. Experience supporting regulatory submissions, interacting with the FDA and/or global regulatory authorities. Collaborate with Clinical Operations to select, oversee, contract, and manage Biostatistics vendors and contract research organizations.
Scientist, Bioanalysis
Company: Denali Therapeutics
Location: Peninsula
Posted Nov 17, 2023
Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state or local protected class. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Excellent critical thinking and scientific skills, and a demonstrated ability to analyze, interpret, and clearly communicate complex DMPK and BA data. Salary Range: $121,000 - $153,000. Develop PK, ADA, and biomarker bioanalytical methods appropriate for regulated and clinical studies, and engage and manage external CROs on method optimization, assay transfer, qualification/validation, and sample analysis to ensure delivery of bioanalytical results within project timelines. Analyze, interpret, summarize and present large molecule and large molecule-based PK and ADA data to internal and external scientists and project teams. Basic Qualifications: PhD in Biochemistry, Analytical Chemistry, Pharmacokinetics, or related scientific discipline, with 0-3- years of relevant experience OR Master's degree and 3+ years of biotech/pharmaceutical or CRO experience in LBA bioanalysis OR Bachelor's degree and 6+ years of biotech/pharmaceutical or CRO experience in LBA bioanalysis Demonstrated expertise in immunoassay/ligand binding assay techniques for biotherapeutic quantification in complex biological matrices. You will work closely with Therapeutic Discovery, Development Sciences, Clinical Development, and Contract Research Organizations (CROs) to develop ligand binding assay methods for pharmacokinetic (PK) assessment of drug candidates, biomarkers, and anti-drug antibodies (ADA) from in vitro and in vivo samples. Demonstrated ability to work effectively and collaboratively with other scientists on cross-functional Project Teams Excellent oral presentation and written communication skills Preferred Qualifications: Working knowledge of quantitative bioanalytical principles, with GLP/GCP regulated assayexperience Denali is committed to its core company value of unity by creating a diverse and inclusive environment.
Senior Account Executive
Company: Force Therapeutics
Location: Remote
Posted Nov 18, 2023
Force Therapeutics is seeking a Senior Account Executive to join their Sales team, which is crucial in acquiring new clients for their digital care management platform. The role involves client acquisition, management, sales operational excellence, mentorship, strategic partnership building, and providing market insights. The ideal candidate should have at least five years of experience in digital health or healthcare B2B, strong communication and negotiation skills, executive presence, tenacity, and a collaborative mindset. Force Therapeutics offers a competitive benefits package and a transparent compensation structure.
Scientist, Neuromuscular Research
Company: Dyne Therapeutics
Location: Waltham
Posted Nov 17, 2023
Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. Experience with established molecular techniques including qPCR, western blotting, ELISA, immunohistochemistry/immunofluorescence, fluorescence in-situ hybridization, flow cytometry, and confocal microscopy. Strong written and oral communication skills, organization, and multitasking, and working in a highly collaborative and cross-functional research environment. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload. Experience in providing scientific and technical leadership applied to novel assay development, advancing challenging drug discovery programs, and mentoring junior colleagues. LI-Onsite The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Contribute to a culture of strong scientific curiosity and build a positive, team-oriented environment. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned.
Senior Research Associate, Platform Development
Company: Dyne Therapeutics
Location: Waltham
Posted Nov 17, 2023
Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload. Perform biochemical analysis on in-process and final purified conjugates including the following techniques: mass spectrometry (MS), CE-SDS, SDS-PAGE, BCA, SEC-HPLC, and UV-vis Perform Tangential Flow Filtration (TFF) Maintain an electronic lab notebook in a timely manner and contribute to company intellectual property Communicate experimental results to a diverse audience of scientific collaborators Serve as functional area representative on cross-functional drug discovery teams Write technical reports to support documentation and technical transfer Contribute to critical discussions of therapeutic structure, function, and new targets Education and Skills Requirements: Minimum of a B.Sc in chemistry, chemical biology, or biochemistry and 4 years of experience in drug discovery and development, preferably at a clinical stage biotechnology company; or M.Sc and 2 years of experience Demonstrated understanding of the general principles of chemistry/biochemistry Demonstrated proficiency in synthesis, purification, and characterization of protein bioconjugates Demonstrated track record of contributions to research including the ability to work independently and troubleshoot experiments Demonstrated ability to collaborate and contribute to an inclusive and high-functioning team Understand published scientific literature outside of his/her immediate area of expertise and apply this understanding to drive innovation Prepared scientific publications or regulatory submission documents LI-Onsite The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Primary Responsibilities Include: Independently plan and execute multistep bioconjugation reactions to deliver protein-oligonucleotide conjugates, including Preparation of activated oligonucleotides and APIs Execution of protein-oligonucleotide conjugations across protein and payload classes up to multi-gram scale Purification of protein conjugates utilizing AKTA FPLC systems with a variety of different chromatography modes (including CHT, HIC, etc.) The employee may be requested to perform different or additional duties as assigned. This role is based in Waltham, MA without the possibility of being a remote role. The successful candidate will work within a group of bioconjugate chemists, biochemists, and analytical scientists, generating and presenting their own data. This position may change or assume additional duties at any time. All Employees are expected to adhere to all company policies and act as a role model for company values.
Senior/Principal, IP Paralegal
Company: Allogene Therapeutics
Location: Peninsula
Posted Nov 18, 2023
Allogene Therapeutics is hiring a Senior/Principal IP Paralegal to support the legal department on intellectual property matters, focusing on patent matters. The role involves providing legal assistance, coordinating paper and eFiling of patent applications, keeping abreast of rule changes, assisting in patent litigation, and maintaining a contract database. The ideal candidate should have a Bachelor's degree, at least 7 years of relevant experience, and proficiency in MS-Word, Excel, PowerPoint, Outlook, and related software. The company offers a competitive compensation package and a collaborative work environment.
Director, Medical Information
Company: Cerevel Therapeutics
Location: Boston, MA
Posted Nov 17, 2023
This role will require active involvement in strategic planning for product launches, major medical affairs initiatives, and organizational changes, ensuring that all medical information responses are accurate, balanced, evidence-based, non-promotional, and compliant. Reporting to the Senior Director of Medical Capabilities, the Director of Medical Information will be responsible for developing, executing, and overseeing the strategic growth of the Medical Information department, as well as determining the most effective approach for building Medical Information capabilities, either in-house or through outsourcing to vendors. Key Responsibilities Collaborate with the Senior Director of Medical Capabilities to plan, design, and execute the strategic scale-up and development of the Medical Information function Develop a set of requirements and standard operating procedures (SOPs) for handling medical information requests, updating them as industry best practices evolve Determine whether Medical Information capabilities should be developed in-house or outsourced to a vendor and make data-driven recommendations Manage resources to meet Medical Information requirements, working with cross-functional teams to produce standard and custom response documents Ensure that all responses are accurate, balanced, scientifically supported, non-promotional, and compliant with industry regulations and company standards Oversee relationship with Medical Information vendor (if applicable) and ensure their performance meets company standards Create training materials and conduct training for Medical Information staff, evaluating their comprehension and competence in partnership with the Medical Affairs team Define key performance metrics for success in the Medical Information function and regularly assess and report on progress Develop and maintain standards, templates, and a company lexicon for standard and custom response documents Oversee the management and maintenance of the Medical Information website to ensure accurate and up-to-date dissemination of medical information to healthcare professionals Stay updated on relevant scientific and medical literature to anticipate and respond effectively to queries Identify opportunities for process improvements and modifications to enhance the quality, efficiency, and productivity of medical information operations Develop and manage budgets for outsourcing resources and internal staffing, ensuring expenditures align with budgetary guidelines Determine staffing level adjustments based on workloads, cost justifications, and operational needs, and make staffing recommendations to Medical Affairs leadership This role does not currently have direct reports but will be responsible for building out the Medical Information capability as the organization grows Required Qualifications PharmD, PhD or MD in life sciences with a minimum of 6 years bio-pharmaceutical industry experience within Medical Information Desired Qualifications Significant experience in Medical Information, Medical Affairs, or related roles within the pharmaceutical or biopharmaceutical industry Strong leadership and team management skills Deep understanding of industry regulations and compliance requirements Familiarity with medical review processes Excellent computer skills with a strong proficiency in Microsoft 365 programs, as well as Veeva systems Exceptional communication skills, both written and verbal, with the ability to understand and effectively communicate scientific and clinical data to key stakeholders Ability to set priorities, deal with ambiguity and ability to be independent, multi-tasked and results-oriented with a hands-on attitude in a fast-paced and energetic environment Education PharmD, PhD or MD Cerevel is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other characteristic protected by applicable law. Role Summary: The Director of Medical Information will play a pivotal role in building, scaling, and leading the Medical Information function at Cerevel Therapeutics. Cerevel aspires to develop and nurture a culture characterized by trust, respect, courage, curiosity, and compassion, with a relentless focus on mission and results. Headquartered in the Greater Boston area, we are bold thinkers, deep experts, resilient pathfinders, and transparent partners who push the boundaries of scientific understanding to unlock breakthrough CNS therapies that have real impact on people’s lives. Our patient-centricity guides our purpose, how we treat each other and what we work on every day. Our portfolio of pre-commercial neuroscience assets targets a broad range of central nervous system (CNS) disorders, including schizophrenia, epilepsy, Parkinson’s disease and substance use disorder. The successful candidate will bring their own unique thinking and approach to Cerevel while sharing our core values and convictions. We are tackling neuroscience diseases with a differentiated approach that combines expertise in neurocircuitry with a focus on receptor selectivity.
Associate Director, Statistical Programming
Company: Dyne Therapeutics
Location: Waltham
Posted Nov 17, 2023
Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. Primary Responsibilities Include: Lead and manage the statistical programming activities for clinical trials and studies, ensuring high-quality deliverables and adherence to timelines Collaborate with biostatisticians, data managers, and cross-functional teams to define programming strategies and requirements Develop, validate, and maintain analysis datasets (CDISC standards), tables, listings, and figures, TLFs) in accordance with regulatory guidelines and internal standards Review statistical analysis plans (SAPs) to provide feedback and strategy to the team to execute the plans Perform complex statistical analyses and simulations using SAS, and R, to support clinical trial design and data interpretation Provide expertise in statistical programming for regulatory submissions (e.g., FDA, EMA), including electronic submission standards (eCTD) Build and maintain software agnostic solutions/macros to automate repetitive tasks. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload. Provide novel solutions to the Biometrics and cross-functional teams to better understand the data Mentor and provide guidance to junior programmers, ensuring their growth and development within the team Stay current with industry trends, best practices, and emerging technologies in statistical programming and data analysis Education and Skills Requirements: Bachelor's or advanced degree in statistics, biostatistics, computer science, or a related field Minimum of 8 years of experience in statistical programming within the pharmaceutical or biotech industry Proficiency in SAS and R is essential; experience with Python is desirable Strong knowledge of CDISC standards (SDTM, ADaM) and regulatory requirements for clinical trials Demonstrated leadership and project management skills, including the ability to lead cross-functional teams Excellent communication and interpersonal skills Detail-oriented with a commitment to data accuracy and quality Ability to adapt to changing priorities and manage multiple projects simultaneously LI-Onsite The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. This role assists the Head of Statistical Programming to contribute to departmental strategies and helps to drive the development and continuous improvement of departmental procedures, training, and standards. This position serves as the program team point person for statistical programing and data standards, provide consultation to the program teams, and be responsible for building a statistical programming team to support the Dyne clinical portfolio. For more information, please visit https://www.dyne-tx.com/, and follow us on Twitter, LinkedIn and Facebook. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned.
Scientist I, Bioinformatics
Company: Scribe Therapeutics
Location: East Bay
Posted Nov 21, 2023
All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, disability, age, or veteran status. The offered pay range will depend on internal equity and the candidate’s relevant skills, experience, qualifications, training, and market data. git), and workflow management (e.g. We will provide an intellectually stimulating, collegial and fast-paced environment. Computational Biology, Bioinformatics, Biophysics, Systems Biology, Genomics, or equivalent) 2+ years experience developing novel algorithms/analysis methods for integrative analysis of genomics or other biological datasets 2+ years experience in computational and statistical programming (python or R preferred), unix command line, bioinformatic toolkits, version control systems (e.g. Visit us at www.scribetx.com. At the time of posting, the base pay wage range for this role is $115,000- 138,000 per year. version control, workflow management, metadata tracking) Foster a driven, fast-paced, dynamic, and fun environment in which to do rigorous science Required Skills and Background: PhD in a quantitative discipline (e.g. nextflow) Strong quantitative reasoning, statistical analysis, and data visualization skills, with a demonstrated ability to apply them to scientific problems Strong working knowledge of bioinformatic file types and public genomics databases Strong working knowledge of next generation sequencing platforms and molecular biology of sample preparation Preferred Skills and Background: Familiarity with CRISPR technologies and therapeutic approaches Familiarity with protein or RNA structure and engineering approaches Experience deploying code in AWS cloud environment (EC2, S3, etc.) If you are ready to engineer the future of therapeutics, then we are excited to hear from you!