- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- ** Director , Biostatistics Early Clinical Development Gene Therapy** The Director of Biostatistics provides leadership and guidance as the statistical ... with Strategic Project Teams on clinical and regulatory strategies for clinical development , and to represent statistical issues in regulatory agency… more
- University of North Carolina- Chapel Hill (Chapel Hill, NC)
- …and leading new early phase clinical trials based upon the science of Gene Therapy Center members. The new director 's plans for fulfilling the Gene ... This position will have an administrative role as the Director for the UNC Gene Therapy Center,...development . The UNC School of Medicine created the Gene Therapy Center in 1993 with the goal of… more
- Lilly (Boston, MA)
- …drug product (labeled and packaged for clinical use) in support of clinical development programs. Verify that drug products are labeled and packaged ... creative solutions to support communities through philanthropy and volunteerism. The Sr. Director , Clinical Supply Management is responsible for setting the… more
- Bio-Techne (Minneapolis, MN)
- …treat and prevent disease worldwide.** We are seeking a tenacious and results-driven Senior Director to lead our Enterprise Cell and Gene Therapy marketing and ... purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides...acquisition, and elevating the awareness of our Cell & Gene Therapy brand. This candidate will possess a strong… more
- Astellas Pharma (Northbrook, IL)
- …Lead the development and execution of Translational Medicine strategy in the development of Astellas's Cell and Gene Therapy assets. Candidates should have ... and biomarker development plans and defines patient selection strategies for clinical studies + Provides key specifics on the mechanism of action, biomarker… more
- UCLA Health (Los Angeles, CA)
- Description Under the supervision of the Director of the Human Gene and Cell Therapy Facility (HGCTF), the HGCTF Manufacturing Associate (SRA) is responsible for ... specifications. The purpose of the HGCTF is to manufacture clinical grade gene and cellular therapy products...clinical trials, and to perform scholarly research and development when appropriate. These objectives are to be met… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …that corroborate or inform the biology for decision-making purposes and enable clinical development programs. Evolving Genetic Medicines modalities include RNA ... Interference (RNAi), CRISPR gene editing, AAV gene delivery, and others. As a Medical Director...* Leads the cross-functional study team to craft novel clinical development strategy for genetic medicines, including… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …that corroborate or inform the biology for decision-making purposes and enable clinical development programs. Evolving Genetic Medicines modalities include RNA ... Interference (RNAi), CRISPR gene editing, AAV gene delivery, and others. As a Medical Director.... Leads the cross-functional study team to craft novel clinical development strategy for genetic medicines, including… more
- University of Colorado (Aurora, CO)
- Associate Director or Director of Clinical ...two years of experience in Oncology and/or Cell and Gene therapies. + Certified as a Clinical Research ... of Colorado Anschutz Medical Campus** **Department: Gates Institute** **Job Title: Associate Director or Director of Clinical Research** **Position #:… more
- Lilly (IN)
- …**Purpose and Role** Lilly is seeking an individual with expertise in early clinical development , including clinical pharmacology, to join a passionate ... of basic research strategies, clinical candidate compound selection, and pre- clinical development . + Work with Brand Team/Business Unit colleagues to… more
- Editas Medicine (Cambridge, MA)
- …transition from process characterization and clinical manufacturing to late-stage clinical and commercial manufacturing of CRISPR gene editing medicines. The ... allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We believe our people are at the core of everything we do,… more
- Premera Blue Cross (Mountlake Terrace, WA)
- …functional areas across the company. The Director will oversee the development of pharmacy clinical quality and provider engagement programs, clinical ... that we serve through our Healthsource blog: https://healthsource.premera.com . As the ** Director of Pharmacy and Clinical Consulting** , you will participate… more
- Sanofi Group (Cambridge, MA)
- … expertise in respiratory/immunology field + Has a demonstrated track record in clinical development , with Phase 3 experience being an advantage + Understands ... you thought was possible. Ready to get started? The Clinical Research Director (CRD), Amlitelimab, Immunology and...Immunology and Inflammation Therapeutic Area is responsible for the development , execution and reporting of clinical trials… more
- University of Southern California (Los Angeles, CA)
- … Director Process DevelopmentApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/cGMP-Associate- Director ... Facility. The successful candidate will work on the process development and manufacture of cell and gene ...with current Good Manufacturing Practices (cGMP). As the Associate Director of Process Development , the individual will… more
- Lilly (Indianapolis, IN)
- …for the development and implementation of biological assays in support of clinical development and regulatory submission. The candidate will be expected to ... life better for people around the world. The Bioproduct Research and Development (BR&D) organization strives to deliver creative medicines to patients through the… more
- Editas Medicine (Cambridge, MA)
- …activities. The successful candidate will apply their knowledge, expertise and drug development experience to advance our gene editing platform. The ... the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We believe our people are at the...with the program team's objectives at all stages of development . This individual will also be responsible for developing… more
- AbbVie (North Chicago, IL)
- …AbbVie's Development Biological Sciences department is seeking a Scientific Director for its Portfolio Leadership Group. The primary function of this role ... nonclinical safety functional area subject matter expert. + Articulate and communicate non- clinical safety strategies and provide development plans for multiple… more
- Editas Medicine (Cambridge, MA)
- …to timelines while maintaining high quality performance. Key Responsibilities: As the Senior Director , In Vivo Gene Editing Therapeutics, you will be responsible ... allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We believe our people are at the core of everything we do,… more
- Editas Medicine (Cambridge, MA)
- …allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing. We believe our people are at the core of everything we do, ... role will lead and support the CMC strategies and submission including clinical trials applications, marketing applications, agency briefing packages and response to… more
- Kelly Services (Burlington, MA)
- …to work in a fast-paced, high growth CRO environment serving leading pharma in biologic development and cell & gene therapy. This is a unique opportunity to join ... **Sr. Manager/ Associate Director - Quality Assurance** **Burlington, MA** **Direct Hire**...packages and reports to the Company's external pharma and gene therapy partners. + Ensure appropriate definition, development… more