Associate Director Clinical Pharmacology and Pharmacokinetics
Viking Therapeutics, Inc.
Description The Associate Director Clinical Pharmacology and Pharmacokinetics will play a crucial role in our drug discovery and development efforts, providing integrated pharmacokinetics/pharmacodynamics (PK/PD), toxicokinetics (TK), ADME and clinical pharmacology assessment of Viking’s novel therapies. This role involves managing activities and timelines, analyzing and interpreting pharmacokinetic data from preclinical studies, clinical trials and assisting with preparation and review of scientific and regulatory documents. Essential Duties and Responsibilities The main Clinical Pharmacology and Pharmacokinetics responsibilities of this role include but are not limited to the following: Contribute to all phases of preclinical projects (non-GLP and GLP), from in vitro ADME, in vivo PK, PK/PD, formulations and IND enabling toxicology and TK analysis, along with planning and execution of pivotal in vivo PD and disease animal models Serve as the clinical pharmacology lead across multiple programs, owning the execution of clinical pharmacology plans from IND through early clinical development, including food effect, drug-drug interaction, organ impairment, and QT assessments. Design and oversee PK, PK/PD, and exposure-response analyses to support dose selection, study design, and benefit-risk assessments Perform non-compartmental and compartmental PK/PD analysis, modeling and simulation for preclinical, formulations and clinical studies, in collaboration with CROs, consultants, preclinical and development teams Oversee bioanalysis and PK deliverables, related to protocols, study synopses, preclinical and clinical study reports, briefing books, INDs, IBs, and NDAs. Work closely with Biometrics and external modeling partners to support population PK and exposure-response modeling Stay current with regulatory guidance and scientific advances in clinical pharmacology, applying best practices to development programs Other duties as assigned Requirements Education and Experience Ph.D., Pharm.D., or equivalent in clinical pharmacology, pharmaceutical sciences or a related field with 6+ years of experience or BS/MS level training with 10+ year experience in clinical pharmacology, pharmaceutical sciences or a related field in the biotech or pharmaceutical industry Knowledge and Skills Experience designing and executing early-phase clinical studies, including healthy volunteer studies Strong expertise in PK analysis and exposure-response interpretation Experience in assessing impact of various factors on the PK/PD of novel therapeutics and communicating analyses and recommendations to teams Familiarity with regulatory guidelines relevant to toxicology/TK, clinical pharmacology and pharmacokinetics Knowledge of model-informed drug development, including population PK, PK/PD modeling, and exposure-response Proficiency with PK/PD modeling and statistical analysis platforms like Phoenix WinNonlin, Gastroplus, Matlab, Simulations Plus etc. Excellent communication, leadership and teamwork skills VIKING THERAPEUTICS Viking Therapeutics, Inc., is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Viking Therapeutics also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Notice to Agency and Search Firm Representatives Viking Therapeutics, Inc. is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Viking employee by a third-party agency and/or search firm without a valid written & signed search agreement, and assignment of specific position, will become the sole property of Viking Therapeutics, Inc. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. #J-18808-Ljbffr
$173.6k - $237k
...tardive dyskinesia, chorea associated with Huntington's disease,... ...compounds in mid- to late-phase clinical development across our core... ...: Provides Clinical Pharmacology scientific support for one... ..., and reporting of pharmacokinetic (PK), pharmacodynamic (PD),...SuggestedContract work$166k - $208k
...Associate Director, Clinical Pharmacology page is loaded## Associate Director, Clinical Pharmacologyremote type: Remotelocations: Remotetime type:... ...Determine scope, design, plan, and analyze phase 1-4 pharmacokinetic and pharmacodynamics studies* Champion model-informed...SuggestedLocal area- A biotechnology firm located in California is seeking an Associate Director of Clinical Pharmacology and Pharmacokinetics to manage drug development processes. This role involves leading clinical pharmacology plans, performing pharmacokinetic analyses, and overseeing study...Suggested
- ...Associate Director, Pharmacometrics, Clinical Pharmacology Our client is seeking talented individuals who will thrive in our collaborative, diverse, fast-paced environment and share in our mission - to identify, develop and deliver life-changing therapies to people...SuggestedShift work
- ...A leading pharmaceutical company in San Diego seeks an Associate Director, Clinical Pharmacology to develop and execute clinical strategies for drug development. The role involves collaborating with teams to design studies and prepare regulatory submissions. Ideal candidates...SuggestedRemote work
$160k - $200k
...engine and a robust preclinical and clinical development pipeline. We are... ...others.**Position Summary:**The Associate Director, In Vivo Pharmacology, will be responsible for providing... ...experiments to evaluate the efficacy, pharmacokinetics, and safety of therapeutic...Local areaWeekend work$138.6k - $257.4k
...Senior Principal Scientist / Associate Director, PK Sciences, Therapeutic Areas (DUAL... ...develop and implement translational or clinical pharmacology strategies to support the pursuit of... ...continuum, providing expert pharmacokinetic / drug metabolism and clinical pharmacology...Work at office$199k - $248.7k
...days per week on average. Position Summary The Director of Clinical Pharmacology will bring deep expertise across both preclinical and... ...Standard Operating Procedures (SOPs) for all clinical pharmacokinetic-related studies Work with the quality assurance team...Work at officeLocal areaRemote workNight shift3 days per week$200k - $225k
...Director, Pharmacometrics & Clinical Pharmacology Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops... .... Requirements Doctoral degree (PhD, PharmD) in pharmacokinetics, pharmacology, pharmaceutical sciences, or a...- ...The Associate Director, Clinical Study Management, will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required. This role will require a minimum of 3 days a week of onsite presence (or more as business needs...Contract workWork at officeFlexible hours3 days per week
$200k - $225k
...outside of the liver, and our clinical pipeline includes disease targets... ...Pharmaceuticals is seeking a Director of Pharmacometrics and Clinical Pharmacology to provide strategic and scientific... ...degree (PhD, PharmD) in pharmacokinetics, pharmacology, pharmaceutical sciences...- ...Bristol-Myers Squibb is looking for an Associate Director, Cross Functional Clinical Operations in San Diego. This role will lead cross-functional operational execution for RayzeBio RPT assets, focusing on treatment site onboarding and operational visibility. The ideal...
- A leading biopharmaceutical company in San Diego is seeking an Associate Biostats Director to lead statistical analysis for clinical studies. This role requires extensive experience in SAS programming, along with strong leadership skills and the ability to provide statistical...Remote job
$190.54k - $230.89k
...our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: RayzeBio is seeking an Associate Director, In‑Vivo Pharmacology to provide scientific and operational leadership across oncology programs with a focus on radiopharmaceutical therapeutics...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeImmediate startRemote workFlexible hours$190k - $200k
...About Artiva: We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our... .... For more information, visit Job Summary: The Associate Director, Clinical Operations will manage clinical trials as part of...Work experience placementFlexible hours$172.67k - $209.23k
...day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. The Associate Director, Cross Functional Clinical Operations is responsible for leading and supporting cross‑functional operational execution for RayzeBio RPT...Hourly payFull timeTemporary workSummer workImmediate startFlexible hours$155k - $190k
...Job Title: Associate Director, Clinical Data Systems and Informatics Location: San Mateo, CA; San Diego, CA Position Summary The Associate Director, Clinical Data Systems and Informatics will contribute to the development of our diagnostic tests through management of...$160k - $230k
...creates, acquires and finances companies that develop and commercialize pharmaceutical products. Position Summary The Associate Director, Clinical Program Management (CPM) is responsible for leading assigned clinical studies to support Aurinia’s clinical development...Local area$190.54k - $230.89k
Bristol Myers Squibb is seeking an Associate Director, In‑Vivo Pharmacology in San Diego to lead scientific and operational efforts in oncology programs. This role requires deep expertise in in-vivo pharmacology, strong leadership capabilities, and a commitment to drug...$144k - $179.6k
...hybrid model requires this role to work in our office three days per week on average. Position Summary The Associate Director will collaborate with the Clinical Data Management team by providing leadership and knowledge. Assists the head of Data Management in directing...Contract workLocal areaRemote workNight shift3 days per week- ACADIA Pharmaceuticals Inc. is seeking an Associate Director in San Diego, CA. This role involves overseeing the Clinical Data Management team, ensuring high-quality data deliverables for various studies, and collaborating on clinical protocol design. Candidates should...
$170.6k - $255.8k
...yourself, and in this hybrid role you will serve as both the Clinical Technical Lead and R&D Portfolio Manager for on‑market... ...Compensation & Benefits Estimated base salary range for the Associate Director, Clinical On‑Market R&D Program Manager role based in the United...Local area- kps life in San Diego, California is seeking an Associate Director for the Data Management team. This role involves overseeing clinical data collection studies, ensuring the integrity and quality of data deliverables for regulatory submissions. The ideal candidate holds...Contract work
$173.6k - $237k
...includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal... ...robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades...$100k
## Associate Clinic DirectorApplylocations: Chula Vista FHC - San Diego, CA: Rice FHC - San Diego, CAtime type: Full timeposted on: Posted... ...Health Centers of San Diego is looking for an Associate Clinic Director (ACD). Under the direction of the Clinic Director, the ACD...Full timeLocal area- ...Executive Medical Director, Early Clinical Development At Lilly, we unite caring with discovery... ...Collaborate with clinical pharmacology, biostatistics, regulatory affairs,... ...approaches, clinical pharmacology, and pharmacokinetic/pharmacodynamic modeling Previous...
- Location: San Diego, CA. Key Responsibilities Mitigate access and reimbursement disruptions through education of office staff on payer coverage and policies, and acquisition pathways. Educate offices in navigating access and reimbursement challenges independently through...Work at officeLocal area
$106k - $176.6k
...Clinical Pharmacology Lead Will join a team of scientists supporting oncology development programs. Will be the Clinical Pharmacology... ...PD analyses. Is responsible for integrating knowledge of pharmacokinetics, pharmacodynamics, patient characteristics, and disease states...H1bLocal areaVisa sponsorshipWork visaRelocation packageFlexible hours2 days per week- ...Adagene Inc. (Nasdaq: ADAG) is a platform-driven, clinical-stage biopharmaceutical company committed to transforming the discovery and development of novel antibody-based cancer immunotherapies. Adagene combines computational biology and artificial intelligence to design...Local area
$254.6k - $347k
...Medical Director The Medical Director will play a critical role in advancing clinical programs by partnering with Clinical Operations, Regulatory Affairs, Drug Safety... ...medicine, biomarker development, and clinical pharmacology principles. Strong scientific, analytical...Contract work
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