Jobs at Click Therapeutics
249,921 open positions
Director of Program Management
Company: Dragonfly Therapeutics
Location: Waltham
Posted Aug 29, 2023
Dragonfly Therapeutics is seeking a Director of Program Management with a strong scientific background in Oncology, Immunology, or Immuno-oncology. The role involves leading cross-functional program teams, collaborating with key stakeholders, and managing multiple programs in parallel. The successful candidate will have a degree in life sciences, at least 10 years of industry experience, and strong leadership skills.
Clinical Data Manager I
Company: Click Therapeutics
Location: New York City, NY
Posted Aug 31, 2023
Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Click Therapeutics in the U.S. and, if so, whether that authorization permits them to work in the job they seek. Click Therapeutics will conduct interviews face-to-face over Zoom. If someone contacts you about a job or position that is not listed on the official career page, please contact the Click Therapeutics recruitment team at the contact information below. If you have any questions regarding the validity of a recruitment inquiry or an interview, please contact the Click's recruitment team at [email protected] to confirm before proceeding. Competitive Salary with Annual Review | Annual Performance-Based Cash Bonus | Stock options | 5% 401(k) matching | Comprehensive Medical Benefits | Dental | Vision | Voluntary Benefits | Unlimited PTO | Uber One | Nectar Rewards | One Medical | Fertility Support | Gym Pass | Citi Bike | Professional Development Stipend | Weekly Grubhub Lunches | Generous Paid Parental Leave | Industrious Workspaces | Commuter Subsidies | Choice of Mac or Windows | Sponsored Company Events | Office Snacks and Beverages | Much More...Equal Employment OpportunityClick Therapeutics is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Click Therapeutics may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residency and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons. All job postings will be listed on the Click Therapeutics official career page. Other than your email address or telephone number, which you may provide via a job application portal, Click Therapeutics will never ask you to provide personally identifiable information about yourself (such as a Social Security Number or Driver's License Number) via a messaging application (like that used on the LinkedIn platform or Microsoft Teams). This role will support database design/development, medical coding, data systems and quality, and vendor oversight. We have a hybrid working model that consists of at least 3 days in office each week.Responsibilities Understanding of clinical data, efficiencies in managing its collection, oversight of its management and assurance of its integrity in the clinical trial process Contribute to the oversight of external service providers, the development, implementation and maintenance of appropriately validated systems/applications for clinical data management, and for providing data management support for clinical trials Contributes to protocol design, study build, validation, clinical databases and data validation activities Creates and maintains project documentation, including, but not limited to, Data Management Plan, CRF Completion Guidelines and validation specifications Designs, modifies and manages study eSource documents Generates routine and ad-hoc reports using internal and external data sources Prepares and distributes project status reports to project team and management Contributes in the development, review, and implementation of departmental SOPs, Work Instructions, templates, guidelines, etc.
Legal Contracts Specialist II
Company: Vividion Therapeutics
Location: San Diego, CA
Posted Aug 29, 2023
The job summary is for a Legal Contracts Specialist II position at Vividion Therapeutics, Inc. The role involves managing the company's contract management system, providing system support, and participating in the contracting process. The candidate should have 3+ years of contract experience and a Bachelor's degree. The position offers a competitive salary, benefits, and relocation assistance.
Manager/ Sr. Manager/Associate Director of Quality Assurance GCP/GCLP/GLP
Company: Dragonfly Therapeutics
Location: Waltham
Posted Aug 31, 2023
Overall, the successful candidate will be a key member of Dragonfly’s talented team and play an important role in bringing novel therapies to patients. Responsibilities:Lead the nonclinical/clinical QA function to develop and implement a quality system in accordance with ICH Guideline E6 (R2) Good Clinical Practice (GCPs), 21 CFR part 58 Good Laboratory Practices (GLP), and other global regulatory authority requirements, and industry practicesDevelop and implement QA GLP/GCLP/GCP systems, risk management processes, and SOPs for internal and external oversight operationsOversee QA review and approval of GLP and GCLP study protocols and reports, clinical study reports, ICFs, external publications, and regulatory submissions (i.e., IND/IMPD)Collaborate and provide QA expertise in processes such as investigations, corrective and preventive action (CAPA) plans, trial protocol deviations, complaints, DSURs, risk management, risk assessments, recalls, safety events/reporting, relevant regulatory submission sections, and trial documentation reviewDevelop and implement an early-stage clinical site quality audit program in collaboration with clinical study teamsLead the nonclinical and clinical vendor, and internal quality audit programsDesign and execute on the audit plans/schedules in collaboration with nonclinical and clinical development teams, including establishment of appropriate quality compliance criteria, to assure compliance with regulations, guidelines, and standardsEnsure the nonclinical and clinical sites are audit ready and compliant at all timesDevelop training materials and conduct trainingGenerate clinical and nonclinical QA metrics and present at senior leadership meetingsQualifications:BS/MS in biology, chemistry, life sciences or related fieldAt least 8+ years’ experience in pharmaceutical / biotech / clinical research industry with significant experience in GLP/GCLP/GCP environment (title commensurate with experience)Previous direct QA experience in GLP/GCLP/GCP in pharma required Prior experience with nonclinical studies and CRO oversightAbility to work in a fast-paced environment, meet deadlines, and balance multiple prioritiesIndependently motivated, detail-oriented, and “can-do” attitudeStrong verbal and written skills; ability to provide focus and clarity; able to handle confidential information and material appropriatelyMust have proficient computer skills and be experienced using MS office software (Word, Excel, PowerPoint, Project)Ability and willingness for approximately 20% travel – domestic and international, consistent with project needsAbout DragonflyDragonfly 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. 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. Our mission is to revolutionize disease treatment by inventing natural killer cell-based therapies for vastly improved patient outcomes. Working closely with the Clinical Operations, Translational Medicine, and Toxicology Teams at Dragonfly, this role will have primary responsibilities for the QA oversight of GLP/GCLP/GCP activities internally, and at its CROs, Clinical Sites, and third-party laboratories and vendors. Reporting to the Head of Quality Assurance, this role will develop and implement a phase-appropriate quality system that supports quality and compliance of clinical and nonclinical activities at Dragonfly. We believe in a small team with a big impact. Manager/Associate Director of Quality Assurance GCP/GCLP/GLPDragonfly Therapeutics is seeking a highly motivated and talented individual to lead the GLP/GCLP/GCP Quality Assurance function. Manager/Sr.
Senior Scientist Translational Sciences
Company: Entrada Therapeutics
Location: Boston, MA
Posted Aug 31, 2023
Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law. Third Party Staffing AgenciesEntrada does not accept unsolicited resumes from any source other than directly from candidates. We value work life balance, you'll benefit from discretionary time off, paternity leave, and an excellent 401(k) package. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes. ), ligand binding assays (ELISA or others), rt-PCR, dd-PCR, Western blot, etc.Experience authoring method and study reports as well as contributing to regulatory documentsExperience as a translational program team representative for therapeutics advancing to an IND submission is a plusThe PerksBy becoming a team member here at Entrada, you’ll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. We also offer a generous transportation stipend to commute as you wish. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Our location in the vibrant and growing Seaport District is close to all the best that the city of Boston has to offer. Entrada Therapeutics is an equal opportunity employer. Scientist IIExcellent oral and written communication skills, including writing, reviewing, and editing scientific documentsWork and drive decision-making within a versatile, multi-regional, and matrix organizationPositive, can do attitude (agile, curious, open-minded, "can-do" mindset); needs to clearly demonstrate ability to remove obstaclesAbility to be scientifically independent and manage workload and expectationsPreferred experienceTrack record of success and measurable contribution in moving therapeutic programs forward through preclinical and clinical development in an academic or industry setting especially in the area of oligonucleotidesWorking knowledge of best practices and current guidance from health authorities for bioanalytical method and biomarker analysisHands on experience with data analysis including binding affinity (BLI, SPR, etc. ResponsibilitiesThe successful candidate will focus on non-clinical biomarkers assay transfer and qualification to manage the data quality of the non-clinical translational works for regulatory submission (IND, etc.) and internal records.Work closely with the Product Development team including Biomarkers, Bioanalytical, DMPK and Toxicology to ensure alignment of activitiesMentor scientist(s) and research associate(s) in the Translational Team.Oversee method qualification activities in the Translational Team including detection range (LOQ and HOQ), calibration curve, QCs, selectivity/specificity, sensitivity, accuracy, precision and stability/recovery as applicable.Contribute to authoring and review of internal stage-gate documents including method qualification reports and sample analysis reports for regulatory and/or discovery purposes.Lead the data quality control and data integrity processes in the Translational Team for all data under the responsibility of the team.If needed, communicate with the clinical translational team and work with the non-clinical biomarker team to support answering specific translational questions. THE NECESSITIESAt Entrada, our passion for science, our devotion to patients and our values drive our behavior:Humanity - We genuinely care about patients and about one anotherTenacity - We are relentless and persistent in the pursuit of developing therapies for patients.Creativity - We are creative problem solvers.Collaboration - We are more than the sum of our parts.Curiosity - We have a growth mindset and push conventional thought and theory.To thrive on our team, you will need to come with:PhD degree in a scientific discipline with 4-6 years of industry/post-doctoral experience for a Sr.
Product Manager, Marketing
Company: Corcept Therapeutics
Location: Peninsula
Posted Aug 29, 2023
Corcept Therapeutics, a company dedicated to cortisol modulation, has been pushing scientific boundaries for 25 years. They have developed over 1000 proprietary selective cortisol modulators, including Korlym, the first treatment for Cushing's syndrome. The company values diverse perspectives and aims to revolutionize treatment for severe endocrine, oncology, metabolism, and neurology disorders. The Product Manager role involves strategic marketing responsibilities, HCP strategy and content development, and collaboration with cross-functional departments. The ideal candidate should have a strong understanding of traditional and non-traditional marketing channels, experience in pharmaceutical or biotechnology, and 2-4 years in brand management.
Sr. Scientist II, Research Production Core
Company: Scribe Therapeutics
Location: East Bay
Posted Aug 29, 2023
Scribe Therapeutics is seeking a highly creative, passionate, and motivated individual to join their team as a Sr. Scientist II. The role involves managing high-throughput production screening of research grade viral vectors, coordinating with internal teams and external CROs, and supporting development activities across multiple early-stage programs.
Director, Digital & Omnichannel Marketing
Company: Corcept Therapeutics
Location: Peninsula
Posted Aug 29, 2023
Advanced degree (M.B.A., PhD.) )Experience optimizing owned properties (CortisolMatters.com, Korlym.com/hcp, Korlym.com) to enhance user experience, streamline content and capture data (i.e. ), as relates to digital marketing effortsCollaborate with IT, Corporate Comms. )Experience creating digital infrastructure (CRM, marketing auto., data ecosystems & optimization software)Experience with personal/non-personal, branded/unbranded and digital omni-channel promotionDemonstrated ability to drive cross-functional consensus with complex concepts and initiativesDemonstrated ability to translate strategic direction into effective digital promotion tacticsExperience partnering with marketers and directing agencies of record, for digital promotion and mediaAdditional Qualifications Bachelor’s degree required. is advantageous.10+ years of biopharmaceutical experience with 5-10 years in patient/provider marketing, marketing operations and/or digital/omni-channel marketing. clear calls to action)Expert digital media optimization (SEO, web, programmatic), experience designing multi-touch attribution and/or “next best action(s)” and has led digital media strategy (paid, owned & earned)Digital content creation experience (developed strong pull tactics to engage patients/providers)Has built owned, on-demand learning properties/portals for providers (or patients) that includes content from disease state education, speaker decks and virtual webinar sessionsExperience building /patient databases of qualified leads and CRM programs leveraging optimized owned properties and experience building data base of leads and CRM programs leveraging owned properties.Subject matter expert on emerging trends in digital marketing practices and emerging regulatory trendsExpert ability to create and monitor digital metrics via strategic dashboards (customer conversion rates) , tactical optimization (unique visitors, bounce rates, customer conversion rates, etc. New product launch experience is preferred.Marketing or Marketing Ops experience in a combination of small and large biopharmaceutical companiesAdvanced understanding of relevant legal, regulatory and business compliance considerations is required.Experience working in startup or emerging biopharmaceutical firms is desiredExcellent interpersonal skills with ability to lead, interact with, focus, resolve conflict and drive consensus among individuals from a variety of cultures, and disciplines. The position will be based in Menlo Park/Bay AreaThe pay range that the Company reasonably expects to pay for this position is $218,000 - $257,000; the pay ultimately offered may vary based on legitimate considerations, including job-related knowledge, skills, experience, and education. mobile number and email, NPI)Developed content that drives to owned properties (e.g. and others to gain alignment on cross-functional initiativesDesired Experiences Established and led cross-functional forums to build digital marketing infrastructure & plans; established governance and use-case roadmaps (phased and clear near/mid/long-term plans)Broad digital channel management & integration experience (social, web, email, etc. 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. Applicants 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
Senior Manager/Associate Director, Program Management
Company: Click Therapeutics
Location: New York City, NY
Posted Aug 31, 2023
Click Therapeutics is seeking a Senior Manager/Associate Director, Program Management to lead a cross-functional team in delivering a best-in-class digital therapeutics (DTx) program. The role involves managing project plans, leading meetings, and ensuring program success on time and on budget. The candidate should have 8-12+ years of experience in Program Management, Business Development, or Management Consulting with a focus on the life sciences industry. The position offers a competitive salary, annual performance-based cash bonus, and a generous equity package. The role is based in Tribeca, NYC, with a hybrid working model.
Sr. Manager/ Associate Director of Statistical Programming
Company: Dragonfly Therapeutics
Location: Waltham
Posted Aug 29, 2023
Dragonfly Therapeutics is seeking a highly motivated and talented Sr. Manager/ Associate Director to lead the statistical programming function. The successful candidate will be a key member of Dragonfly's talented team and play an important role in bringing novel therapies to patients.
IT Network Engineer
Company: Shape Therapeutics
Location: Seattle, WA
Posted Aug 29, 2023
ShapeTX is seeking a talented IT Network Engineer to build a Network Operations practice from the ground up. The role involves designing, implementing, and maintaining corporate networks, managing network interconnections, and collaborating with cross-functional teams. The ideal candidate should have a Bachelor's degree in a relevant field, at least 3+ years of professional experience in enterprise network solutions, and proficiency in Palo Alto Networks firewalls, Cisco Meraki, and AWS networking. The company offers a robust benefits package and a competitive salary range of $96,000-$144,000.
Senior Manager/Associate Director, Program Management
Company: Click Therapeutics
Location: New York City, NY
Posted Aug 31, 2023
Click Therapeutics is seeking a Senior Manager/Associate Director, Program Management to lead a cross-functional team in delivering a best-in-class digital therapeutics (DTx) program. The role involves managing project plans, leading meetings, and ensuring program success on time and on budget. The candidate should have 8-12+ years of experience in Program Management, Business Development, or Management Consulting with a focus on the life sciences industry. The position offers a competitive salary, annual performance-based cash bonus, and a generous equity package. The role is based in Tribeca, NYC, with a hybrid working model.