Pharmacist (Pharmacologist) Highland County Joint TownshipPharmacist (Pharmacologist)Ohio, ILAs a member of the Medicaid Pharmacy team, your responsibilities will include: Providing expert advice and assistance to pharmacists participating in the Ohio Medicaid Program, including development of prior authorization criteria. Licensed to practice pharmacy as issued by State Board of Pharmacy, pursuant to Section 4729.12 of Revised Code; 2 yrs.
In Vitro Pharmacologist Integrated Resources, IncIn Vitro PharmacologistGroton, ConnecticutContractorJob responsibilities include performing routine tasks associated directly with the Cystic Fibrosis projects or indirectly in a capacity easing role to support these projects. · The Primary Pharmacology Group is actively supporting Cystic Fibrosis projects in developing assays, running subset screens, and external data management.
Lead Clinical Pharmacologist Integrated Resources, IncLead Clinical PharmacologistGroton, ConnecticutPart timeLeads multifunctional study team to design, deliver and report the assigned clinical pharmacology studies and has overall scientific accountability for the designated studies. • Plans and directs clinical pharmacology components of clinical programs (including clinical development plan/life cycle plan) and studies (including synopsis preparation; clinical phase oversight, reporting).
In-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. Job responsibilities include: Performing routine tasks associated directly with the Cystic Fibrosis projects or indirectly in a capacity easing role to support this and other projects.
Pharmacist (Pharmacologist) State of OhioPharmacist (Pharmacologist)Columbus, OHAs a member of the Medicaid Pharmacy team, your responsibilities will include: Providing expert advice and assistance to pharmacists participating in the Ohio Medicaid Program, including development of prior authorization criteria. Licensed to practice pharmacy as issued by State Board of Pharmacy, pursuant to Section 4729.12 of Revised Code; 2 yrs.
Senior Clinical Pharmacologist Regeneron PharmaceuticalsSenior Clinical PharmacologistCambridge, MA$128,600–$210,000 / yearAs 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 Affairs teams. Performs analyses such as compartmental modeling, PopPK, translational modelling, disease modelling, Pop PK/PD, E-R analyses (or work closely with Research Specialist or Pharmacometrics Stats Programming team) to deliver Pharmacometrics results, interpretation and discussion.
Remote | Clinical Pharmacologist (PK/PD & Dose Strategy) — $110–$160/hour 24-MagRemote | Clinical Pharmacologist (PK/PD & Dose Strategy) — $110–$160/hourNew York, New YorkRemoteSelected experts will help develop clinically plausible PK/PD datasets, dosing and escalation regimens, exposure-response relationships, and pharmacology-focused reference materials that remain consistent with efficacy and safety outputs. We are sharing a specialised part-time consulting opportunity for experienced clinical pharmacologists with substantial expertise in pre-market drug development, PK/PD analysis, dose selection, exposure-response modelling, and clinical pharmacology strategy.
NewClinical Pharmacologist Writer DRT Strategies, Inc.Clinical Pharmacologist WriterSilver Spring, MD$80,000–$105,000 / yearPreparation of these documents, including ensuring appropriate and consistent formatting, quality checking for accuracy of data summaries, and compliance with Section 508 requirements for reader accessibility, has historically been the responsibility of medical officers (MOs), regulatory project managers (RPMs) and their supervisors, who are also responsible for primary review of data and analyses contained in the submissions. Project Description: CBER expects to receive biologics licensure applications (BLAs) for vaccines, and high-profile and complex BLAs and BLA efficacy supplements for non-COVID-19 vaccines and other products.
NewAssociate Director Clinical Pharmacology Senior Clinical Pharmacologist Oncology AbbVie IncAssociate Director Clinical Pharmacology Senior Clinical Pharmacologist OncologyNorth 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).
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).
NewAssociate Director Clinical PharmacologySenior Clinical Pharmacologist Oncology AbbVie IncAssociate Director Clinical PharmacologySenior Clinical Pharmacologist OncologyWaltham, MASenior 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 Oncology AbbVie IncSenior Clinical Pharmacologist OncologySan Francisco, CAPhD 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). Participate and present at various departmental and cross functional teams such as study teams, clinical pharmacology and biopharmaceutics, clinical strategy team, Clinical Pharmacology leadership team, Journal club.
Senior Clinical Pharmacologist Specialty AbbVie IncSenior Clinical Pharmacologist SpecialtyNorth Chicago, ILPhD 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). Participate and present at various departmental and cross functional teams such as study teams, clinical pharmacology and biopharmaceutics, clinical strategy team, Clinical Pharmacology leadership team, Journal club.
Senior Clinical Pharmacologist AbbVie IncSenior Clinical PharmacologistNorth Chicago, ILPhD 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). Participate and present at various departmental and cross functional teams such as study teams, clinical pharmacology and biopharmaceutics, clinical strategy team, Clinical Pharmacology leadership team, Journal club.
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).
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.
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.
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.
Associate Director / Senior Associate Director, Clinical Pharmacology Lead Boehringer Ingelheim International GmbHAssociate Director / Senior Associate Director, Clinical Pharmacology LeadRidgefield, CT$140,000–$222,000 / yearClinical 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, pediatric drug development and using MIDD approach for drug development. Delivering Results: Under the supervision of senior clinical pharmacologists 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.