Tessera Therapeutics

Position OverviewTessera is seeking an experienced physician with expertise in hematology to serve as the Medical Monitor for our innovative Gene Writing clinical programs. This individual will provide medical oversight across clinical studies ensuring patient safety protocol complian

Position OverviewTessera is seeking an experienced physician with expertise in hematology to serve as the Medical Monitor for our innovative Gene Writing clinical programs. This individual will provide medical oversight across clinical studies ensuring patient safety protocol complian

Your experience includesBachelors degree in a relevant scientific or healthcare discipline with 8 years of clinical operations experience including 4 years as a clinical trial manager leading cross-functional teams and accountable for planning and executing global clinical trials.Expe

Your experience includesBachelors degree in a relevant scientific or healthcare discipline with 8 years of clinical operations experience including 4 years as a clinical trial manager leading cross-functional teams and accountable for planning and executing global clinical trials.Expe

Your experience includesPhD in Analytical Chemistry or related discipline e.g. Biochemistry Biotechnology or Pharmaceutical Science with 0-3 years of industry experience in biotech pharmaceutical and/or CROs. Postdoc experience is a plus.Hands-on Experience in LC-MS based bioanalysis

Your experience includesPhD in Analytical Chemistry or related discipline e.g. Biochemistry Biotechnology or Pharmaceutical Science with 0-3 years of industry experience in biotech pharmaceutical and/or CROs. Postdoc experience is a plus.Hands-on Experience in LC-MS based bioanalysis

Your experience includesJ.D. from a fully accredited law school.15 years of industry-related experience with 5 years in-house experience at a biopharmaceutical company with rare diseases business strongly preferred.Good standing and licensed to practice law in one or more U.S. states.

Your experience includesJ.D. from a fully accredited law school.15 years of industry-related experience with 5 years in-house experience at a biopharmaceutical company with rare diseases business strongly preferred.Good standing and licensed to practice law in one or more U.S. states.

Your experience includesPhD with 5 years of experience in academic or industry setting MS with 10 years of experience or BS with 12 years of experienceBroad knowledge of genome editing technologies and associated off-target discovery assays (i.e. WGS; targeted sequencing; GUIDE-seq Di

Your experience includesPhD with 5 years of experience in academic or industry setting MS with 10 years of experience or BS with 12 years of experienceBroad knowledge of genome editing technologies and associated off-target discovery assays (i.e. WGS; targeted sequencing; GUIDE-seq Di

Your experience includesPhD with 5 years of experience in academic or industry setting MS with 10 years of experience or BS with 12 years of experienceBroad knowledge of genome editing technologies and associated off-target discovery assays (i.e. WGS; targeted sequencing; GUIDE-seq Di

Your experience includesPhD with 5 years of experience in academic or industry setting MS with 10 years of experience or BS with 12 years of experienceBroad knowledge of genome editing technologies and associated off-target discovery assays (i.e. WGS; targeted sequencing; GUIDE-seq Di

Your experience includesScientific background in biology chemistry or a related life sciences discipline with a strong understanding of biotech pharmaceutical or life sciences R&D workflows.Experience configuring or supporting an ELN LIMS registry or scientific workflow platform (e.g.

Your experience includesScientific background in biology chemistry or a related life sciences discipline with a strong understanding of biotech pharmaceutical or life sciences R&D workflows.Experience configuring or supporting an ELN LIMS registry or scientific workflow platform (e.g.