Jobs at Click Therapeutics
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Region Manager, Southwest
Company: Corcept Therapeutics
Location: Peninsula
Posted Nov 15, 2023
An annual cash bonus and equity grants may be provided as part of the overall compensation package, in addition to a full range of medical, financial, and other wellness benefits, dependent on the position offered. LI-RemoteApplicants must be currently authorized to work in the United States on a full-time basis.If you are based in California, we encourage you to read this important information for California residents linked here.Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs. Please visit our website at: https://www.corcept.com/Corcept is an Equal Opportunity Employer Our vibrant community is made up of over 300 people—medical practitioners, scientists, and industry professionals—all with the shared goal of advancing the science of cortisol modulation to treat serious disease.Our work has uncovered over 1000 proprietary selective cortisol modulators, including our marketed product, Korlym® (mifepristone), the first treatment available for those living with Cushing’s syndrome, a life-threatening condition caused by excess cortisol activity. Today, we have a unique opportunity to revolutionize the treatment of severe endocrine, oncology, metabolism and neurology disorders and aim to deliver better outcomes for the people affected by them.The RM will manage a team of Clinical Specialists (CS) and provide consistent direction regarding the execution of sales and marketing strategies for the Southwest region.Responsibilities: Formulate sales strategies and analyze performance within the regionFully engage with key customers by developing and implementing strategies that support sales growthProvide on-going coaching and development of CSS teamDevelop and maintain customer relationships with key executives and decision makers in all key accountsParticipate in and contribute to commercial team planning sessions as requested, representing the needs of customers and the sales team and driving business building plans of the organizationAct as local liaison and collaborator, building consensus on strategies and tactics that drive business resultsOperate within compliance guidelines at all timesPreferred Skills, Qualifications and Technical Proficiencies:Proven success in leading a sales team within a large geographyExperience in endocrinology, orphan disease, or other specialized markets a plusStrong clinical acumenAbility to analyze sales and other relevant market data to formulate strategic plansStrong ability to collaborate and work cross-functionallyRequired to travel by car and plane at least 80% of the timePreferred Education and Experience:Must maintain a driving record in accordance with Corcept vehicle policyMaster’s Degree in a life science or related field or equivalent experienceThe pay range that the Company reasonably expects to pay for this position is $190,000 - $215,000; the pay ultimately offered may vary based on legitimate considerations, including job-related knowledge, skills, experience, and education. That is why for twenty-five years we have pushed the boundaries of what is possible, driven by fiercely independent science, open collaboration and the curiosity to follow the data wherever it leads.Our company is committed to building a culture that values diverse perspectives and the unique contributions of every employee. At Corcept Therapeutics, we believe the potential impact of cortisol modulation on the future of health has long gone overlooked.
Senior Software Prototype Engineer
Company: Click Therapeutics
Location: New York City, NY
Posted Nov 17, 2023
Click Therapeutics is a leading innovator in Digital Therapeutics, developing and commercializing software as prescription medical treatments for various unmet medical needs. The company focuses on psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. They are seeking a full-stack software development engineer to join their R&D team, responsible for prototyping software solutions for mobile applications. The ideal candidate should have 4+ years of experience, strong coding and design skills, and the ability to work collaboratively in a dynamic environment. The role offers a competitive salary, annual performance-based cash bonus, and a generous equity package, along with comprehensive benefits.
Director, Quality Assurance Commercial Operations
Company: CymaBay Therapeutics
Location: North Jersey
Posted Nov 16, 2023
Excellent written, oral and interpersonal communication skills. Strong attention to detail, excellent organization skills and cultural fit. Identify, communicate, and escalate quality and compliance risks. Proficiency in Microsoft Office applications Ability to operate in a fast-paced, multi-disciplinary virtual environment. Demonstrated success in coaching, mentoring and training across functions. Self-directed, juggle multiple tasks and strong ability to work effectively with cross-functional teams. Proven technical writing/editing skills and problem-solving ability. Experience leading deviation and non-conforming material investigations. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Ability to think and act strategically.
Clinical Research Coordinator
Company: Click Therapeutics
Location: Boston, MA
Posted Nov 17, 2023
Click Therapeutics is a leading innovator in Digital Therapeutics, developing and commercializing software as prescription medical treatments for various unmet medical needs. The company is committed to technical and scientific rigor, patient-centric design, and advanced data-driven tools like AI and machine learning. Click Therapeutics is currently seeking a Clinical Research Coordinator to facilitate and coordinate early clinical research operations and clinical trials. The role involves managing logistics, scheduling, timelines, deliverables, reporting requirements, documentation, and work plans for each project. The ideal candidate should have a Bachelor's degree, preferably in Psychology, Neuroscience, or a related scientific discipline, and at least 1 year of experience as a Clinical Research Coordinator in a biotech, pharma, or CRO setting. The position offers a competitive salary, annual performance-based cash bonus, and a generous equity package, along with comprehensive benefits and a flexible work arrangement.
People & Culture Partner (Contract Position)
Company: Scorpion Therapeutics
Location: San Francisco, CA
Posted Nov 17, 2023
We do not discriminate for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Beginning October 13, 2021, Scorpion Therapeutics requires all new hires to be fully vaccinated against COVID-19. Excellent interpersonal and conflict resolution skills Experience dealing with sensitive, complex, and highly confidential employee situations. Ability to forge, grow and maintain positive relationships with multiple groups. Foster a sense of onsite community by supporting crucial corporate culture initiatives including company cocktail hours, team outings, milestone celebrations, etc. Ability to react quickly to changes, while keeping alignment with long-term direction Motivated by complexity and challenges; energized by evolving, exciting environments. Manage low–lift office operations including managing relationships with building management, partnering with certain team members to order supplies, creating processes around parking and mail management. If you are unable to receive the vaccine due to a disability or serious medical condition, or because of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation. Strong analytical, critical thinking, troubleshooting, problem-solving skills, and a high degree of accuracy and attention to detail Thorough knowledge of employment-related laws and regulations Excellent oral and written communication skills Experience with HR / payroll software systems Computer proficient with experience in Outlook and Microsoft Office Highly organized and detail oriented Scorpion Therapeutics Inc. is an Equal Opportunity Employer who strives to create and maintain a diverse working environment. Qualifications: 3+ years’ experience in human resources, culture and community or related position Bachelor’s degree in human resources or business administration preferred.
Engineering Manager
Company: Force Therapeutics
Location: Remote
Posted Nov 14, 2023
Force Therapeutics is a SaaS, digital therapeutics platform that assists hospitals and surgeons in managing healthcare outside traditional systems. They have collaborated with renowned academic hospital systems like Geisinger, MGB, Dartmouth, and Scripps. Their clinical platform has been validated in numerous research studies, and financial results have been proven at large healthcare systems. The company values teamwork and hires passionate individuals for an important journey to improve healthcare delivery. They are seeking an Engineering Manager with a background in web and mobile technologies, who can guide technical direction, grow a high-performing team, and ensure high-quality, scalable software delivery. The ideal candidate should have experience in frontend, backend, and native mobile engineering, and be familiar with AWS services and engineering best practices.
Sr. Accounting Manager
Company: CymaBay Therapeutics
Location: North Jersey
Posted Nov 16, 2023
Proficiency in Word, Excel, and PowerPoint. Working knowledge of payroll accounting, Concur and ADP a plus. Self-starter, strong work ethic, able to work independently with minimal supervision. The anticipated salary range in Newark, California is $165-180K. Collaborate, communicate concisely, and work cross-functionally with finance personnel, department managers, auditors, accounting consultants, and other stakeholders as necessary. Desire to continuously learn and improve finance processes, systems and controls. CPA certification required. Working experience with inventory accounting auditing and Coupa a plus. Minimum of 1 year of inventory accounting working experience. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc.
Engineer/Sr. Engineer, Upstream Process Development
Company: Dragonfly Therapeutics
Location: Waltham
Posted Nov 16, 2023
Candidate must be independent, goal-oriented, flexible, and able to work efficiently across multiple projects. In addition to its wholly owned clinical assets, Dragonfly has a deep pipeline of wholly owned preclinical candidates discovered using its proprietary platform, as well as productive collaborations with Merck, AbbVie, Gilead and Bristol Myers Squibb in a broad range of disease areas. Responsibilities: Lead development of robust and scalable upstream processes for biologics in different stages of clinical development, including design, execution, analysis, and documentation of all stages of cell-culture process development Support external manufacturing with technology transfer for implementation of new processes and provide person-in-plan support as required Support process change controls, deviations, impact assessments, and perform batch record review Improve upstream processes through research and innovation, while assessing technologies and industry best practices Review, collect and trend data from manufacturing batches to help identify trends, assess performance, build process understanding, and enable improvement activities Champion compliance and safety; promote a culture of diversity, inclusion, and equity Maintain good communication and collaborate with cross-functional colleagues and external partners for successful execution/completion of projects Author and contribute to IND/IMPD/BLA submission Qualifications: BS/MS with 10+ years, or PhD with 2+ years of industry experience and background in Chemical/Biochemical engineering, or a related field Strong fundamental knowledge and subject matter expertise in cell-culture process development, fed-batch cell culture, bioreactors across scales, as well as recent advances, and challenges in the field Experience and aptitude to lead, work and collaborate in internal and external cross-functional, matrixed teams Working knowledge of cGMP and quality systems Action-oriented mindset, ability to take initiative, innovate, iterate and problem solve Experience with cell culture and predictive modeling (omics, metabolic flux analysis); statistics, data-science, machine learning, artificial intelligence a plus Ability and willingness for approximately 10% domestic travel consistent with project needs About Dragonfly Dragonfly Therapeutics is a clinical-stage biopharmaceutical company committed to discovering, developing and commercializing therapies that use its novel multispecific antibody technology to harness the body's immune system to bring breakthrough treatments to patients. The successful candidate will contribute and drive our upstream cell culture process development, while interacting regularly with other CMC functions. We believe in a small team with a big impact. Engineer, Upstream Process Development Dragonfly Therapeutics seeks an upstream process development engineer who brings enthusiasm, intellectual curiosity, scientific rigor and a desire to help deliver novel immunotherapy programs. Our mission is to revolutionize disease treatment by inventing natural killer cell-based therapies for vastly improved patient outcomes. Engineer/Sr. The successful candidate will excel in a highly collaborative work environment with a multi-disciplinary and diverse team focusing on multiple programs in parallel.
Sr. Accountant
Company: CymaBay Therapeutics
Location: North Jersey
Posted Nov 16, 2023
Self-starter, strong work ethic, able to work independently with minimal supervision. Desire to continuously learning and improve finance processes, systems, and controls. Collaborate, communicate concisely, and work cross-functionally with finance personnel, department managers, auditors, accounting consultants, and other stakeholders as necessary. The anticipated salary range in Newark, California is $105K-120K. Strong written and verbal communication and interpersonal skills Proficiency in Word, Excel, and PowerPoint Late development stage, or commercial Biotech experience and working experience with inventory accounting, auditing and Coupa a plus. CPA training / certification a plus. Assess, streamline, and improve operational accounting policies and procedures to ensure efficiency and cost effectiveness. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Ability to work in a team-oriented environment. CymaBay is a multi-state employer, and this salary range may not reflect positions that work outside of the Bay Area or in other states.
Senior Financial Analyst (NetSuite Experience Required)
Company: Scorpion Therapeutics
Location: Boston, MA
Posted Nov 15, 2023
We do not discriminate for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Beginning October 13, 2021, Scorpion Therapeutics requires all new hires to be fully vaccinated against COVID-19. Ability to present financial information to a non-financial audience, excellent communication, interpersonal, and presentation skills. 3-5 years of proven experience in financial planning, analysis, and modeling is required. High aptitude in Excel Modeling. Biotech experience and experience with NetSuite preferred. Strong analytical thinking and problem-solving skills. Qualifications: Bachelor's degree in finance, accounting, or a related field (MBA preferred). Help develop, apply, and implement the best tools to analyze data including sophisticated Excel financial models and planning analytical tools. If you are unable to receive the vaccine due to a disability or serious medical condition, or because of your sincerely held religious beliefs, you will have an opportunity to request a reasonable accommodation.
Senior Director, QA (QMS)
Company: BlueRock Therapeutics
Location: Cambridge
Posted Nov 17, 2023
quality polices, manuals, etc. SOPs, WI, JA etc.) Must demonstrate strategic thinking, excellent organizational skills and be able to drive project teams forward while having a willingness to do hands on work to achieve goals Must be adaptable, flexible and able to work under high pressure and fast moving environment, Demonstrates calmness and decisiveness under pressure, with the ability to bring others along Strong technical writing skills (procedures, policies) with working knowledge of MS office programs, such as Word, Excel, SharePoint, and Adobe Acrobat professional are required Must be self-motivated with the demonstrated ability to work effectively with people from multiple departments, ensure deadlines are met, and manage multiple, potentially changing, priorities. ), documentation, including metrics, dashboards, readouts in support of Quality Oversight, including an overall picture of the health of BlueRock's overall Quality management System in collaboration with the SVP, Quality Assurance Grow & lead a team of quality professionals responsible for managing our process related to documentation and training and providing high levels of support for the enterprise as it relates to achieving documentation and training deliverables. Previous experience with analytics for use in managing quality issues enabling a risk-based approach Experience with implementation of electronic quality management systems is desired, Veeva experience preferred. Collaboration with a highly-motivated, world-class team of scientists, engineers, as well as quality & compliance professionals dedicated to enabling our teams to deliver on bringing life changing medicines to patients, promises an exciting and engaging work environment for a motivated, self-starting candidates, that can strategically design, build, implement and adapt processes and approaches as the organization evolves. Check us out on Comparably: https://www.comparably.com/companies/bluerock-therapeutics Follow us on Linkedin: https://www.linkedin.com/company/bluerocktx/ Equal Opportunity Workplace: At BlueRock, we welcome and support differences and diversity and we are proud to be an equal opportunity workplace. This includes the ownership of technologies and vendors that support these areas as well as defining measurable outcomes to indicate that the processes are delivering as needed Serve as the lead on development of programs to drive a risk-based and outcomes focused Quality Management System, supporting compatibility and integration of quality processes driven core principles, Data Integrity, Scientific Integrity, Patient safety and Product Integrity Support the development of Governance related processes (e.g. Influence and guide in a collaborative fashion, across all aspects of the quality organization partnering with peers to enable quality processes within their space as well as establishing supportive partnership across the organization where appropriate Other duties as assigned Minimum Requirements: Minimum of a Bachelor’s degree in Biology or relevant scientific or engineering discipline Minimum of 10-12+ years of experience in a quality role, preferably implementing and overseeing QMS within a broader quality organization for a life sciences organization supporting development programs (biotechnology, cell & gene therapy) Minimum 10 years in a personnel managing role with demonstrated ability to mentor and develop staff and achieve goals through empowering teams. The Quality System applies to the development, production and testing of cell therapies and medical devices under current Good Manufacturing Practices (cGMP) as well as preclinical (GLP), clinical activities (GCP), and compliance as well as support a broader GVP ecosystem through our parent company Bayer at the enterprise level.
Associate Director, QA Operations
Company: Corcept Therapeutics
Location: Peninsula
Posted Nov 16, 2023
Proficient computer skills are needed with experience using Microsoft Word, Excel, PowerPoint, and Visio. Thorough knowledge of 21 CFR 210/211 global cGMP regulations, and ICH guidelines regarding good manufacturing practices in the development, manufacturing, testing, delivery, and control of pharmaceutical products. Ability to author, review, and approve SOPs and other controlled documentation for compliance with applicable regulations. An annual cash bonus and equity grants may be provided as part of the overall compensation package, in addition to a full range of medical, financial, and/or other wellness benefits, dependent on the position offered. The pay range that the Company reasonably expects to pay for this position is $175,000 - $207,000; the pay ultimately offered may vary based on legitimate considerations, including job-related knowledge, skills, experience, and education. Ability to lead or support internal and external compliance audits of suppliers, CLOs, and CMOs. Travel required Preferred Education and Experience: Bachelors or Masters degree in a chemistry, biology, engineering or related field. Lead and support Contract Service Provider (CSP) qualification audits that can include contract manufacturers, contract testing organizations, distribution depots, PV service provider, and pharmacy. Generate, review, and negotiate Quality and Technical Agreements with Contract Service Providers (CSP). If you are based in California, we encourage you to read this important information for California residents linked here.