NewIn Vitro Pharmacologist Integrated Resources, IncIn Vitro PharmacologistGroton, ConnecticutContractorThis position is with my direct clientJob DescriptionOur Client is looking for "In-Vitro Pharmacologist" with knowledge of "High Throughput Screening" and "Assay Development"Job Summary-· The Primary Pharmacology Group is actively supporting Cystic Fibrosis projects in developing assays, running subset screens, and external data management.· He/she should be adept at multi-tasking, integrating biology concepts from group discussions and the literature, and comfortable working in a team environment.· 4-7 years of experience in Assays studies· Experience in High Throughput Screening and plate based assay
Pharmacologist US Department of Health and Human ServicesPharmacologistWashington, DC$121,785–$191,352 / yearThe Food and Drug Administration is the regulatory, scientific, public health, and consumer protection agency responsible for ensuring that all human and animal drugs, and medical devices are safe and effective, that cosmetics, foods, food additives, drugs and medicated feeds for food producing animals, and radiation emitting devices are safe, and that all such products marketed in the United States are adequately, truthfully and informatively labeled and safely and properly stored, transported, manufactured packaged and regulated. Foreign Education: If you are using education completed in foreign colleges or universities to meet the qualification requirements, you must show that the education credentials have been evaluated by a private organization that specializes in interpretation of foreign education programs and such education has been deemed equivalent to that gained in an accredited U.S. education program; or full credit has been given for the courses at a U.S. accredited college or university.
NewIn-vitro pharmacologist Integrated Resources, IncIn-vitro pharmacologistGroton, ConnecticutFull timeExperience in the high content imaging space, high-throughput screening (HTS) techniques, and automation is advantageous and comfort with relevant software tools such as IDBS Biobook, ABase, Spotfire, and GraphPad Prism is preferred. This is a Direct Hire role with the clientJob DescriptionThe Primary Pharmacology Group is actively supporting Cystic Fibrosis projects in developing assays, running subset screens, and data analysis and management.
NewLead Clinical Pharmacologist Integrated Resources, IncLead Clinical PharmacologistGroton, ConnecticutFull timeLeads the resolution of clinical pharmacology queries from regulatory agencies, takes a lead role in writing and reviewing responses to regulatory queriesQualifications• PhD or Pharm D -At least 10 years of general drug development experience in the pharmaceutical industry• At least 5 years' experience in clinical pharmacology work in the pharmaceutical industry• Demonstrated success in managing global clinical pharmacology activities• Experience in biopharmaceutic aspects of formulation development• Experience in interactions with regulatory agencies globally• Considerable organizational awareness (inter-relationship of departments, business priorities, etc.)Additional InformationWith RegardsRicky Bansal732-429-1925I'm interested Assures that assigned CP study(ies) fulfils its role in the overall development plan• Plans, designs and oversees clinical pharmacology studies as required with operational assistance from Clinical Research Operations• Accountable and responsible for assigned synopsis and study report content• With study team, tracks emerging clinical pharmacology profile of the drug, keeps line management informed of changes in the profile as they occur in the assigned study(ies)• Must be fully knowledgeable about the clinical pharmacology profile of allocated drugs on which studies are being conducted or which are called for in the protocol.•
Associate Director Clinical PharmacologySenior Clinical Pharmacologist AbbVie IncAssociate Director Clinical PharmacologySenior Clinical PharmacologistNorth Chicago, ILSenior Clinical Pharmacologist: PhD with 0 years of experience, or Pharm D with 2+ years of experience in a relevant field, Master's Degree or equivalent education and typically 8+ years of experience, Bachelor's Degree or equivalent education and typically 10+ years of experience; (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters). PhD with typically 4+ years of experience or Pharm D with typically 6+ years of experience in a relevant field, Master's Degree or equivalent education and typically 12+ years of experience, Bachelor's Degree or equivalent education and typically 14+ years of experience;(*relevant field includes experience with PK, PBPK, PK-PD,Pharmacometrics or systems pharmacology, Drug metabolism/Transporters).
Senior Clinical Pharmacologist Regeneron PharmaceuticalsSenior Clinical PharmacologistWarren, MichiganHas understanding of advanced PMx concepts and techniques, such as advanced pharmacokinetics, advanced pharmacological principles, non-compartmental analysis methods, Exposure-Response analysis methods, translational modelling/pharmacology, Nonlinear Mixed Effects modeling, logistic regression, survival analysis, Bayesian approaches, disease modelling/QSP. As a Senior Clinical Pharmacologist this individual is expected to plan, design, implement and analyze in-vivo and in-vitro pharmacokinetic & pharmacodynamic studies working with Clinical Pharmacology, Quantitative Pharmacology, Pharmacometrics/Pharmacodynamics (PK/PD), Toxicology, Bioanalytical, Therapeutic Focus areas and Clinical Development / Regulatory.
Software Engineer OncoHealthSoftware EngineerPrimary Responsibilities Develop software solutions by studying information needs; conferring with users; studying flow, data usage, and work processes; investigating problem areas; following the software development lifecycle. Additional preferred skills include Experience with enterprise workflow platforms, familiarity with CI/CD and Azure DevOps and exposure to AI-driven development workflows.
Principal Investigator / Sr. Principal Investigator, Clinical Pharmacology & Pharmacometrics Incyte CorpPrincipal Investigator / Sr. Principal Investigator, Clinical Pharmacology & PharmacometricsWilmington, DEDemonstrated a general understanding of general DMPK disciplines in vitro ADME pharmacokinetics transporter DDI translational modeling biotransformation biomarker strategy is a plus Demonstrated publication record leadsenior author contributions is a plus Ability to prioritize and manage multiple projects while meeting project deadlines. Through the discovery development and commercialization of proprietary therapeutics Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology Oncology and Inflammation and Autoimmunity Headquartered in Wilmington Delaware Incyte has operations in North America Europe and Asia.
Director, Head of Program Management Tessera Therapeutics IncDirector, Head of Program ManagementSomerville, MA$186,000–$239,000 / yearCompany Summary: Tessera Therapeutics is pioneering Gene Writing- a new biotechnology designed to offer scientists and clinicians the ability to write small and large therapeutic messages into the genome, thereby curing diseases at their source. Guiding and empowering Program Managers to drive the development and management of integrated program plans (including timelines, assumptions, scenarios, risks, critical path, decision maps, goals, and budget drivers).
Software Engineer Oncology Analytics IncSoftware EngineerDevelop software solutions by studying information needs; conferring with users; studying flow, data usage, and work processes; investigating problem areas; following the software development lifecycle. Additional preferred skills include Experience with enterprise workflow platforms, familiarity with CI/CD and Azure DevOps and exposure to AI-driven development workflows.
SVP, Clinical Development Amylyx Pharmaceuticals IncSVP, Clinical DevelopmentCambridge, MARemote$416,000–$468,000 / yearThe Senior Vice President (SVP) of Clinical Development will provide strategic direction and technical leadership to the clinical development team, including clinical-regulatory development planning, clinical trial design, implementation and execution, clinical data analysis and management, and clinical competitive intelligence. Overall, the main responsibility will be to provide strategic leadership for the clinical and medical aspects for the various programs and work closely with a cross-functional team to align the clinical development plan with the overall development strategy of the relevant products.
AD / Senior AD, Clinical Pharmacology Lead - Remote Boehringer Ingelheim International GmbHAD / Senior AD, Clinical Pharmacology Lead - RemoteRidgefield, CTRemote$140,000–$222,000 / yearDelivering results: Under the supervision of senior clinical pharmacologist in the group, ensures timely delivery of state-of-the-art CP scientific concepts for decision making throughout clinical drug development and registration including all necessary processes and documentation. Clinical Pharmacology development strategies could include assessment of pharmacokinetic/pharmacodynamic (PK/PD), drug interaction, formulation development, dose selection decision, impact of renal/hepatic impairment, food effect on PK, QT prolongation and pediatric drug development.