Jobs at Click Therapeutics
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SAP Data Specialist (Contract)
Company: Allogene Therapeutics
Location: Peninsula
Posted Sep 11, 2023
Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. (E.g., Material Master, BOMs, Recipes, Production Versions, Business Partner, etc. As an equal opportunity employer, Allogene is committed to a diverse workforce. Proven change management and project management competency. Develop LSMW scripts for data mass maintenance. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients. Perform Change Control steps related to Master Data Change Actions. )Drive MRP implementation by collaborating with planning team, setting up test data and conducting training workshops.Facilitate Weekly Governance forum meeting & steward the SAP ECM Data Creation Workflow process.Maintain data creation forms, data dictionary and training documents. Responsibilities include, but are not limited to:Create and maintain Master Data elements in SAP Production, Quality and Development environments.
Region Manager, North East
Company: Corcept Therapeutics
Location: Peninsula
Posted Sep 10, 2023
Corcept Therapeutics, a company dedicated to cortisol modulation, has been pioneering this field for 25 years. They have developed over 1000 proprietary selective cortisol modulators, including Korlym, the first treatment for Cushing's syndrome. Their team of over 300 professionals, including medical practitioners, scientists, and industry experts, strive to advance cortisol modulation science for treating serious diseases. They aim to revolutionize treatment for severe endocrine, oncology, metabolism, and neurology disorders. The Role of the Regional Manager (RM) involves leading a team of Clinical Specialists, formulating sales strategies, and engaging with key customers to drive business growth. The RM must have proven success in leading sales teams, strong clinical acumen, and the ability to collaborate cross-functionally. The pay range for this position is $190,000 - $215,000, with potential for bonuses and equity grants.
Chief Human Resources Officer
Company: Scribe Therapeutics
Location: East Bay
Posted Sep 12, 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.At the time of posting, the base pay wage range for this role varies according to level, per year. The pay range offered will depend on internal equity and the candidate’s relevant skills, experience, qualifications, training, and market data. Additional incentives are provided as part of the complete package in addition to comprehensive medical and other benefits. Visit us at www.scribetx.com. We are committed to creating a diverse environment and are proud to be an equal opportunity employer. We will provide an intellectually stimulating, collegial and fast-paced environment. Reporting to our CEO, the current role is for a CHRO to lead HR initiatives and support overall company strategy. The candidate should have a passion for prioritizing the company culture while influencing the areas of talent management, employee engagement, change management, organizational and leadership development, and total rewards. Additionally, the candidate would bring expertise in being an advisor to the CEO and other members of the leadership team, as well as the board of directors, particularly the Compensation Committee.The candidate will design and execute a human resources strategy that will support both near and longer-term goals and objectives by leading the development of strategic and scalable talent practices that promote value and culture, drive employee performance and accountability, motivate workers, and attract the best talent.Key Responsibilities:Collaborate with the CEO and the executive team in supporting overall company objectives.Create an engagement and retention strategy, including an appropriate Total Rewards structure, as well as development opportunities to incentivize employees.Develop effective leadership and talent development programs that enhance the overall organizational effectiveness.Ensure the appropriate evolution of the organizational structure to reflect current and future needs of the company. Effectively collaborate with members within a fully integrated team to facilitate execution on projects within established timelines, including total rewards enhancements, updating systems, and managing budget.Promote Scribe’s culture and values, and ensure they are fostered as the company grows.Foster a driven, fast-paced, dynamic, and fun environment in which to do rigorous scienceRequired Skills and Background:Prior experience leading the HR function, with an established track record of delivering results.Deep and broad knowledge of HR processes such as workforce planning, performance management, talent reviews, and change management.BS degree in Human Resources, Business Administration, or related field is highly desired. An MBA or related Masters’ degree is preferred.At least 12 years of experience in HR leadership roles within high growth companiesDemonstrated success in fast paced, innovative biotech/life sciences companies, both privately and publicly held. Ability to work both independently and collaboratively in a fast-paced, interdisciplinary research teamPreferred Skills and Background:Familiarity with scaling up a life science organization.Familiarity with current HR practices including benefits and compensation philosophies and HR compliance.Salary will be commensurate with experience. If you are ready to engineer the future of therapeutics, then we are excited to hear from you! Founded by CRISPR inventors and leading molecular engineers Benjamin Oakes, Brett Staahl, David Savage, and Jennifer Doudna, Scribe is overcoming the limitations of current genome editing technologies by developing custom engineered enzymes and delivery modalities as part of a proprietary, evergreen CRISPR by Design™ platform for CRISPR-based genetic medicine.We are seeking a highly creative, passionate, and motivated individual to join us in our quest to develop the next generation of CRISPR-based therapeutics. Founded by Chief Human Resources OfficerScribe Therapeutics is a molecular engineering company focused on creating best-in-class in vivo therapies that permanently treat the underlying cause of disease. Scribe Therapeutics is a molecular engineering company focused on creating best-in-class in vivo therapies that permanently treat the underlying cause of disease.
Chief Human Resources Officer
Company: Scribe Therapeutics
Location: East Bay
Posted Sep 12, 2023
Scribe Therapeutics, a molecular engineering company, is seeking a CHRO to lead HR initiatives and support overall company strategy. The ideal candidate should have a passion for prioritizing company culture, expertise in talent management, employee engagement, change management, organizational and leadership development, and total rewards. The role involves collaborating with the CEO and executive team, creating an engagement and retention strategy, developing leadership and talent development programs, and promoting Scribe's culture and values. The candidate should have prior experience leading HR functions in high growth companies, preferably in biotech/life sciences, and be familiar with scaling up a life science organization and current HR practices.
Director, Global Event Management
Company: Corcept Therapeutics
Location: Peninsula
Posted Sep 11, 2023
Corcept Therapeutics, a company dedicated to cortisol modulation, is seeking a Director of Global Event Management. The role involves leading corporate event and scientific congress planning, managing exhibit agencies, and overseeing meeting logistics. The ideal candidate should have 10+ years of congress and meeting planning experience, strong interpersonal skills, and a deep understanding of the pharma industry. The pay range is $218,500 - $257,000, with potential for bonuses and equity grants.
Assistant Controller/Controller
Company: Belharra Therapeutics
Location: San Francisco, CA
Posted Sep 11, 2023
Individual pay within that range can vary for several reasons including skills/capabilities, experience, and available budget.Belharra is committed to being an Equal Opportunity Employer and our policy is to provide equal employment opportunities to all applicants and employees without regard to race, color, creed, religion, sex, sexual orientation, gender identity, marital status, citizenship status, age, national origin, ancestry, disability, veteran status, or any other legally protected status and to affirmatively seek to advance the principles of equal employment opportunity.Privacy Act Notice and Policy Statement In this role, you will lead all areas of operational Finance including accounting, financial closing & reporting, payroll, insurance, technical accounting, tax, and audit. You don’t just meet goals, you set the standard.Bachelor’s or master’s degree in a related field with current CPA accreditation required.Big 4 Public Accounting experience required.Minimum of 10 years relevant experience with increasing responsibilities, including a strong focus on general accounting, SEC reporting, systems optimization, job costing, and reporting systems required.Thorough and current knowledge of GAAP accounting principles.Experience with review and preparation of financial statements; payroll and franchise tax filings and requirements.Experience with general ledger functions and the month-end/year end close process.Knowledge and experience with QuickBooks and NetSuite required, and experience with other financial and accounting software systems desired.Experience in developing internal controls and driving implementation of policies and procedures.Experience coordinating quarterly and annual filings, ensuring compliance with GAAP and other regulations.Knowledge and experience with SEC reporting and SOX compliance are a plus.IPO experience highly desired.Ability to timely deliver on responsibilities within a highly collaborative environment.Experience with biotech/tech start up and venture backed industry experience preferred.Ability to make sound, scalable, decisions and create clear processes.WHAT YOU’LL GET AS PART OF OUR TEAMA collaborative and positive culture Limitless growth and learning opportunitiesCommitment to talent and leadership developmentAll Belharrans gain access to the SkillCycle platform and receive the opportunity to work 1:1 with a coach to support their growth and developmentA chance to make a lasting impact on drug discovery and human healthCompetitive compensation and company ownershipExcellent Medical, Dental and Vision coverage from a broad choice of providers and plans 100% of premium coverage for employees; up to 95% of premium coverage for eligible dependents401(k) program with a company sponsored contribution“Take what you need” vacation and sick time off policy10 annual paid company holidays, plus the last week of DecemberOffice space in San Mateo with flexibility and autonomy to do your work how and where you needBelharra is committed to being an Equal Opportunity and our policy is to provide equal employment opportunities to all applicants and employees without regard to race, color, creed, religion, sex, sexual orientation, gender identity, marital status, citizenship status, age, national origin, ancestry, disability, veteran status, or any other legally protected status and to affirmatively seek to advance the principles of equal employment opportunity.Pay Scale Range (CA)$175,000—$225,000 USDAt Belharra Therapeutics, Inc. pay ranges are subject to change and are assigned to a job based on its level within the company. The ideal candidate will have experience as an accountant in our industry, preferably in a senior role, and will report to the Vice President, Finance. WHAT YOU’LL BE RESPONSIBLE FOR Essential duties and responsibilities include the following. Other duties may be assigned.Lead the accounting operations of the company and work directly with internal and external team members and department heads to ensure completeness and accuracy of financial information.Direct day to day financial and accounting functions including overseeing the functions of accounts payable, payroll, revenue recognition, fixed assets, month-end closings, bank and general ledger reconciliations, and accounting.Ensure compliance with internal controls, including the maintenance of documentation, testing procedures and remediation activities.Manage external accountants, contractors, auditors and third-party professional firms, including insurance and tax. The successful candidate will bring an in-depth knowledge of accounting and financial reporting for private and public companies, an understanding of tax and statutory requirements, an ability to collaborate with auditors, tax authorities and business partners. Responsible for preparation of financial updates, analysis and content for certain meetings of the of the Board of Directors, and other external stakeholders.Ad hoc analysis and other special projects as assigned.Help identify and implement system and process enhancements to improve operational efficiencies across the Company.WHAT YOU’LL BRING TO THE TEAMPeople-first approach. You take pride in the way you collaborate and partner with people across the business.Passion for problem solving. Our aim is to deliver transformative, first-in-class medicines for patients suffering from the most serious diseases. WHO WE AREBelharra Therapeutics is an early-stage small molecule discovery company founded by pioneers in the field of chemical biology. Through the application of our proprietary chemoproteomics platform merged with innovative biology and medicinal chemistry, we are modulating protein function in previously unidentified ways to push the limits of drug discovery. Our aim is to deliver transformative, first-in-class medicines for patients suffering from the most serious diseases.WHAT WE ARE LOOKING FORWe are currently seeking a highly motivated Assistant Corporate Controller to join our team. You are excited by new challenges and know how to achieve maximum results and drive projects forward.Thirst for overachieving. Through the application of our proprietary chemoproteomics platform merged with innovative biology and medicinal chemistry, we are modulating protein function in previously unidentified ways to push the limits of drug discovery.
Assistant Controller/Controller
Company: Belharra Therapeutics
Location: San Francisco, CA
Posted Sep 11, 2023
Belharra Therapeutics, an early-stage small molecule discovery company, is seeking a highly motivated Assistant Corporate Controller. The role involves leading all areas of operational finance, including accounting, financial closing & reporting, payroll, insurance, technical accounting, tax, and audit. The ideal candidate will have a Bachelor's or master's degree in a related field with current CPA accreditation, Big 4 Public Accounting experience, and at least 10 years of relevant experience. The company offers a collaborative, fun, and positive culture, competitive compensation, and opportunities for growth and learning.
Associate Director, Process and Product Development
Company: Allogene Therapeutics
Location: Peninsula
Posted Sep 11, 2023
Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. As an equal opportunity employer, Allogene is committed to a diverse workforce. Responsibilities include, but are not limited to:Manage, lead and mentor a high performing team of scientists and provide oversight and technical leadership for the development of formulation, aseptic filling, cryopreservation, drug product container, storage, and post thaw processes and proceduresDevelop robust processes for formulation, fill/finish, and cryopreservation for chimeric antigen receptor T-cell (CAR-T) products utilizing QbD DOE principlesEstablish and qualify representative fill/finish scale-down models to identify CPPs that impact Drug Product CQAsCollaborate with CMC and clinical teams to evaluate dosage form options to enable dosing requirements for in-use dosing and administration stability studies and other TPP objectivesUse risk assessment/management tools and apply QbD principles for successful technology and knowledge transfer to internal and external Drug Product manufacturing sitesLead and facilitate cross-functional activities in support of pipeline priorities by working collaboratively across CAR-T Process Sciences, Analytical Development, Internal/External Manufacturing, Quality, and Regulatory groupsDrive and coordinate studies while managing timelines to meet corporate goalsImplement process advancements for scaling-up and introduction into a GMP manufacturing environmentAct as internal expert and maintain state-of-the-art knowledge in the field of cellular cryopreservation and cryobiologyOther duties as assigned Position Requirements & Experience:Ph.D. in Chemical Engineering, Biochemistry, Molecular & Cell Biology, Immunology or the related field with at least 8 years of relevant experience required 10+ years (or at least 10 years 12+ years with a Master’s degree M.S.) This individual will lead the development, characterization and implementation of state-of-the-art formulation, aseptic filling, and cryopreservation drug product processing technologies to deliver scalable and robust clinical and commercial manufacturing processes. of relevant experience requiredA demonstrated foundational understanding of mammalian or primary cell culture, biochemistry, molecular & cell biology and immunology (required for enhanced product & process understanding)Strong knowledge and hands-on experience with cell therapy process development and cryopreservationFormulation science experience, especially with cryoprotectant additivesStrong scientific understanding of cell biology and cryopreservation Experience working in or supporting a cGMP-regulated environmentExperience in cell therapy manufacturing processesAbility to work in a fast-paced, startup environmentStrong attention to detail with the ability to multi-task and handle multiple responsibilities simultaneouslyExcellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelinesExperienced leader of scientific teamsExperienced project management/leadership skillsStrong interpersonal skills including verbal and written communication are essential in this collaborative work environmentCandidates must be authorized to work in the U.S. We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. All approved Allogene Therapeutics positions are accessible via the Allogene Careers page at www.allogene.com/careers.LI-AW1 We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.Please be aware that the FBI recently issued a warning about an increased number of fake job postings for remote work employment that target applicants' personally identifiable information. For more information, please visit www.allogene.com, and follow @AllogeneTx on Twitter and LinkedIn. About the role:Allogene is seeking an Associate Director, Process and Product Development to lead the Drug Product Team for Allogene’s CAR-T cell therapies.
Associate Director, Process and Product Development
Company: Allogene Therapeutics
Location: Peninsula
Posted Sep 09, 2023
Allogene Therapeutics is hiring an Associate Director, Process and Product Development to lead the Drug Product Team for their CAR-T cell therapies. The role involves managing a team of scientists, developing robust processes for formulation, aseptic filling, and cryopreservation, and collaborating with CMC and clinical teams. The ideal candidate should have a Ph.D. in a relevant field with at least 8 years of experience, strong knowledge in cell therapy process development and cryopreservation, and experience in a cGMP-regulated environment.
Manager, Analytical Development
Company: Corcept Therapeutics
Location: Peninsula
Posted Sep 11, 2023
Corcept Therapeutics is a company that believes in the potential of cortisol modulation to improve health. They have been working on this for 25 years and have developed over 1000 proprietary selective cortisol modulators. They are committed to building a culture that values diverse perspectives and are working to deliver better outcomes for people affected by serious diseases.
Scientist/Sr Scientist, Analytical Development
Company: Strand Therapeutics
Location: Boston, MA
Posted Sep 12, 2023
Strand Therapeutics, an early-stage biotech company, is seeking a highly motivated Scientist/Sr Scientist, Analytical Development. The role involves designing and developing robust assays, driving analytical innovations, and managing test method transfers. The ideal candidate should have a degree in a relevant field, extensive experience in analytical test methods of biologics, and a proven track record in assay development in the gene therapy space. Strand offers a fast-paced, team-focused work environment with a top-notch benefits package.
Associate Director, Process and Product Development
Company: Allogene Therapeutics
Location: Peninsula
Posted Sep 11, 2023
Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. As an equal opportunity employer, Allogene is committed to a diverse workforce. This individual will lead the development, characterization and implementation of state-of-the-art formulation, aseptic filling, and cryopreservation drug product processing technologies to deliver scalable and robust clinical and commercial manufacturing processes. Responsibilities include, but are not limited to:Manage, lead and mentor a high performing team of scientists and provide oversight and technical leadership for the development of formulation, aseptic filling, cryopreservation, drug product container, storage, and post thaw processes and proceduresDevelop robust processes for formulation, fill/finish, and cryopreservation for chimeric antigen receptor T-cell (CAR-T) products utilizing QbD DOE principlesEstablish and qualify representative fill/finish scale-down models to identify CPPs that impact Drug Product CQAsCollaborate with CMC and clinical teams to evaluate dosage form options to enable dosing requirements for in-use dosing and administration stability studies and other TPP objectivesUse risk assessment/management tools and apply QbD principles for successful technology and knowledge transfer to internal and external Drug Product manufacturing sitesLead and facilitate cross-functional activities in support of pipeline priorities by working collaboratively across CAR-T Process Sciences, Analytical Development, Internal/External Manufacturing, Quality, and Regulatory groupsDrive and coordinate studies while managing timelines to meet corporate goalsImplement process advancements for scaling-up and introduction into a GMP manufacturing environmentAct as internal expert and maintain state-of-the-art knowledge in the field of cellular cryopreservation and cryobiologyOther duties as assigned Position Requirements & Experience:Ph.D. in Chemical Engineering, Biochemistry, Molecular & Cell Biology, Immunology or the related field or equivalent experience Relevant experience in the pharmaceutical/biotech industryA demonstrated foundational understanding of mammalian or primary cell culture, biochemistry, molecular & cell biology and immunology (required for enhanced product & process understanding)Strong knowledge and hands-on experience with cell therapy process development and cryopreservationFormulation science experience, especially with cryoprotectant additivesStrong scientific understanding of cell biology and cryopreservation Experience working in or supporting a cGMP-regulated environmentExperience in cell therapy manufacturing processesAbility to work in a fast-paced, startup environmentStrong attention to detail with the ability to multi-task and handle multiple responsibilities simultaneouslyExcellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelinesExperienced leader of scientific teamsExperienced project management/leadership skillsStrong interpersonal skills including verbal and written communication are essential in this collaborative work environmentCandidates must be authorized to work in the U.S. We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. All approved Allogene Therapeutics positions are accessible via the Allogene Careers page at www.allogene.com/careers.LI-AW1 We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.Please be aware that the FBI recently issued a warning about an increased number of fake job postings for remote work employment that target applicants' personally identifiable information. For more information, please visit www.allogene.com, and follow @AllogeneTx on Twitter and LinkedIn. About the role:Allogene is seeking an Associate Director, Process and Product Development to lead the Drug Product Team for Allogene’s CAR-T cell therapies. Led by world-class management with significant experience in cell therapy, our fully integrated, in-house team of researchers is dedicated to discovery and translational research, development, and cell manufacturing.At Allogene, we are developing a pipeline of off-the-shelf CAR T cell candidates, with the goal of delivering readily available cell therapy faster, more reliably, and at greater scale to more patients.