Associate Director/Director, Clinical Pharmacology
Beam Therapeutics Inc.
Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases. Position Overview The Associate Director/Director in Clinical Pharmacology position will support a rapidly expanding clinical portfolio of promising gene/base editing therapeutics. The candidate in this position should have strong scientific and technical skills, be well versed in PK and PD with a strong ability to critically evaluate and interpret data, conduct rapid exploratory analysis, quantitative systems pharmacology (QSP) and PKPD modeling. In this role, the candidate is expected to have strong data analyses, modeling, and critical thinking ability with good oral and written communication skills. The role could be tailored to focus solely on pharmacometrics or could be a hybrid Clinical Pharmacology/Pharmacometrics role based on the candidate’s experience and career aspirations. As a member of the clinical pharmacology department, this person is expected to operationalize model-based drug development, by integrating modeling results into clinical study design, regulatory documents, and internal decision-making. Responsibilities Provide critical input in build-out of the Clinical Pharmacology function, including hiring of personnel and deployment of modeling infrastructure. Operationalize model-based drug development, including new methodology approaches as described in regulatory guidelines. Serve as key functional expert to lead, direct, and coordinate the activities of their assigned modeling projects. Conduct PK and PK/PD analyses and modeling using nonclinical and clinical data. Contribute to protocol and study report writings. Present key pharmacometrics analyses results to internal and external stakeholders. Facilitate model-based drug development across to support BEAM’s clinical programs. Develop and write pharmacometrics analysis plans, execute and author reports on results of analyses. Define and drive pharmacometrics contributions to regulatory/submission strategy and related documents. Provide strategic expertise and leadership for development programs based on relevant technical and disease area knowledge. In collaboration with cross functional partners, provide support for the quantitative evaluation of competing trial/analysis strategies. May manage portfolios at disease area/therapeutic area/indication level to support integration of pharmacometrics and relevant knowledge in the planning and execution of programs and strategies. Preparation of abstracts and manuscripts for publications. Qualifications Ph.D. in Pharmacokinetics, Pharmacology, Pharmacology, Pharmaceutics or other relevant field with 3 to 10 years of experience in pharmaceutical industry, or M.D or Pharm.D. with equivalent experience. Expert knowledge and evidence of hands‑on experience in the application of pharmacometrics methods to drug development. Expertise in pharmacokinetics, PKPD principles, ADME concepts, and clinical pharmacology. Expertise in Phoenix WinNonLin, NONMEM and R, or other pharmacokinetic, modeling and data visualization software. Strong communication skills (verbal and written) and presentation skills are required. Excellent interpersonal skills and the ability to function in a highly matrixed team environment are essential. Experience and willingness to mentor and develop others. Expertise in translational modeling in in‑vivo and ex‑vivo gene editing therapeutics. Curiosity and enthusiasm to adopt to new modeling and data analyst approaches that facilitate new data or scientific insights. #J-18808-Ljbffr Beam Therapeutics Inc.
$185k - $260k
...a vision of providing life-long cures to patients suffering from serious diseases.Position Overview: The Associate Director/Director in Clinical Pharmacology position will support a rapidly expanding clinical portfolio of promising gene/base editing therapeutics. The...SuggestedFull time$154.4k - $242.55k
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$146.3k - $234.1k
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$171k - $236k
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...Position Summary Korro Bio is seeking an Associate Medical Director or Medical Director to provide medical leadership for our clinical programs, with initial focus on KRRO-121... ..., Data Management, Clinical Pharmacology, Regulatory Affairs, Toxicology, and Drug...Interim roleFlexible hours$204k - $306k
Job DescriptionGeneral Summary:The Clinical Development Associate Medical Director will serve as the Medical Lead for clinical trials, working with cross... ...forms, statistical analysis plans, clinical pharmacology analysis plans, and clinical study reportsActs as liaison...Full timeSummer workRemote workFlexible hours2 days per week- ...effectively manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that achieve commercial... ...position can be hired based on the below qualifications: Associate Director, Clinical Pharmacology PhD with typically 4+ years of...Full timeLocal area
$158.6k - $285.5k
The Role This role will support Oncology Therapeutic programs, specifically supporting the Clinical Study Lead in the development, execution and evaluation of Phase 1-3 clinical studies. The principal responsibility for this role is to ensure the comprehensive data quality...Permanent employmentFull timeWork at officeWork from home$144k - $216k
...enormously in the current AI era yet comprises only a portion of the journey to bring new treatments to those in need. The final step - clinical drug development - is oft overlooked, despite requiring a significant proportion of time and investment. In the AI for Clinical...Full timeTemporary workWork experience placement$163k - $225k
About This RoleAs the Associate Scientific Director, Clinical Genetics, you will join our Human Genetics team within Research and Development and help bring human genetics insights into late-stage research and clinical development programs. This role is focused on applying...Full timeTemporary workLocal area$185k - $200k
Who we are.Arbor Biotechnologies, a clinical stage, next-generation gene editing company... ...you, keep reading.About the role. The Associate Director, Bioanalytical Sciences & Biomarkers... ..., partnering closely with In Vivo Pharmacology, Clinical Development, Regulatory, Quality...- ...Planet Pharma GroupContact: ApplicationsEmail: ****@*****.*** SummaryWe are seeking an experienced Associate Director, Clinical Operations to lead the execution of a multinational Phase 2/3 clinical study. This individual will serve as the...
$148.5k - $214.5k
Job title: Associate Director - QSP Quantitative Systems PharmacologyLocation: Morristown, NJAbout... ...highly talented Quantitative Systems Pharmacology (QSP) modeling scientist to support... ...efforts, integrate diverse biological and clinical data, and translate model insights...Full time$175.8k - $237.8k
OverviewThe Associate Director, Quantitative Systems Pharmacology (QSP) will support a rapidly expanding clinical portfolio of promising RNAi therapeutics. The candidate in this position should be well versed in systems pharmacology, clinical pharmacology, PK and PD with...Full timeTemporary workLocal areaFlexible hours$194k - $267k
...) or Huntington’s disease. As a member of the RMD and FA team, the Associate Medical Director will support early and/or late-stage program(s). This role will ensure the successful execution of clinical trials, in line with the strategic plan and assist the team in achieving...Full timeTemporary workLocal area- Reportingto:Sr. Director,Clinical Data Management Do you have the passion and commitment to join a group whose mission is to develop treatments... ...across one or more clinical development programs. The Associate Director will oversee CRO partners and vendors, drive data quality...2 days per week
$194k - $266.75k
...movement disorders (RMD), such as Friedreich ataxia (FA) and Huntington’s disease.As a member of the SMA Clinical Development team, the Associate Medical Director will serve as Study Medical Director for one or more assigned studies, with appropriate oversight, and provide...Full timeTemporary workLocal area$175k - $210k
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Who we are:Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to...Contract work$142.4k - $224.1k
...drives scientific planning, strategy, and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will... ...with global cross functional team members including clinical directors and study managers to lead/support clinical trial scientific activities...Full timeFor contractorsLocal areaFlexible hours
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