Pharmacologist Jobs in the United States
NYU Langone Medical Center
$102610.24 - $171392
Patchogue, NY
The hospital facility is home to theKnapp Cardiac Care Center—an advanced heart disease diagnostic and treatment facility—as well as a modern ambulatory surgical pavilion with specialized services including women's imaging, a sleep laboratory, and bariatric surgery. Duties include obtaining Best Possible Medication History (BPMH), appropriately documenting medication histories in our health systems Electronic Health Record (Epic), and collaborating with the pharmacy team and other healthcare providers as needed.
NYU Langone Health
$102610.24 - $171392
Patchogue, NY
The hospital facility is home to the Knapp Cardiac Care Center—an advanced heart disease diagnostic and treatment facility—as well as a modern ambulatory surgical pavilion with specialized services including women's imaging, a sleep laboratory, and bariatric surgery. Duties include obtaining Best Possible Medication History (BPMH), appropriately documenting medication histories in our health systems Electronic Health Record (Epic), and collaborating with the pharmacy team and other healthcare providers as needed.
Vertex Pharmaceuticals Incorporated
Seattle, WA
General Summary: The Pharmacology Research Scientist works with a high degree of independence and is adept at conceptually outlining studies to design, execute and interpret assays to study the action of compounds on in vitro or in vivo disease biology. This level captures both the Research organization's entry level for staff with a research doctoral degree (PhD) and the advanced experimental expert leading one or more critical laboratory functions with high impact on drug discovery projects.
Boehringer Ingelheim
$140000 - $222000
Ridgefield, CT
Delivering 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.
Kriya Therapeutics
Research Triangle Park, NC
We leverage our proprietary computational engine, in-house manufacturing infrastructure, and integrated design platform to engineer technologies and therapeutics with the potential to transform the treatment of a broad universe of diseases of high unmet need, with a focus on metabolic disorders, neurology, and ophthalmology. We are proud to have been named Triangle Business Journal’s Life Sciences 2024 “Best Private Company to Work For,” recognized by Forbes as one of “America’s Best Startup Employers of 2024,” and honored as one of BioSpace’s “2025 Best Places to Work.”.
Radionetics Oncology, Inc.
San Diego, CA
Radionetics is advancing a pipeline of first-in-class small molecule radioligands targeting Gproteincoupled receptors for the treatment of a broad range of cancers, including breast cancer, lung cancer, and other indications of high unmet need. Radionetics Oncology, Inc. is a clinical stage radiopharmaceutical company focused on the discovery and development of novel radiopharmaceuticals for the treatment of a wide range of oncology indications and is poised to capitalize on the increasing demand for novel radiotherapeutics.
Boston University
$65000 - $70000
Boston, MA
The core program is to translate AD genetics and functional genomics into human brain cells both in vitro 2D and 3D models using human induced pluripotent stem cells (hiPSCs) from population and isogenic lines generated by CRISPR/Cas9 genome editing and in vivo hiPSC/rodent chimera systems in comparison with post-mortem brain. The TCW laboratory (https://sites.bu.edu/tcwlab/) in the Department of Pharmacology, Physiology & Biophysics at Boston University Chobanian & Avedisian School of Medicine in Boston, Massachusetts is looking for highly motivated and skilled stem cell biologists or electrophysiologists to be the drivers of our efforts to translate the genetics of human AD toward therapeutic interventions.
Bristol Myers Squibb
$200000 - $237000
Princeton, NJ
Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
TRILLIANT FOOD & NUTRITION
LITTLE CHUTE, WI
development of products within one or more of the following categories, based on expertise: *Functional beverages *Energy drinks *Dairy-based. JOB REQUIREMENTS: About Us: Trilliant Food & Nutrition is a leading, vertically integrated manufacturer of premium coffees and powdered.
Pfizer
$295900 - $478800
Bothell, WA
Use Your Power for Purpose** + Leads multiple (~2-4) cross functional oncology product teams from pre-clinical candidate nomination (CAN) through Phase 1-2 clinical development and proof of concept (POC) stages, at which point molecule may be handed to the late-stage Oncology Development team for post-POC (typically phase 3) development + In close collaboration with functional experts on the product teams, drives the effective integration of an end-to-end cross functional molecule strategy and risk mitigation plan and ensures delivery of data-driven milestones through successful risk identification and mitigation. + **Demonstrates a passion for helping patients with cancer and for the science of oncology.** + **A proactive and strategic thinker, with strong data-driven decision-making skills** + **Ability to focus and motivate a team in a matrix organization with multiple stakeholders** + **Strong verbal, written, and presentation communication skills** + **Effective mentoring experience and skills** + **Highly collaborative with outstanding relationship building skills with internal company leadership, external development partners and investigators/medical professionals** + **Has a strong leadership presence and the ability to work effectively with other leaders.
ImmunEdge, Inc
Redwood City, CA
Collaborate with discovery, translational, and biomarker teams to leverage study-derived samples and develop ex vivo mechanistic assays (MSD, bulk RNA-seq, scRNA-seq) that inform disease biology, mechanism of action and translational strategy. . Demonstrated ability to independently analyze and interpret complex datasets using Flowjo, GraphPad Prism, generate publication-quality figures, and effectively communicate findings through slide presentations in departmental and cross-functional forums. .
Thorne
Summerville, South Carolina
This role ensures materials meet specifications, supports formulation feasibility and rapid innovation, and drives method robustness, data integrity, and compliance with applicable regulations (e.g., cGMP for dietary supplements, 21 CFR Part 111). Is committed to impartiality and confidentiality in all aspects of laboratory activities, informs management when risks to impartiality and confidentiality are identified and supports taking steps immediately to minimize such risks.
TechDigital Corporation
Miami, FL
2+ years of General Clinical Laboratory experience having a combination of clinical laboratory and either clinical research laboratory or in-vitro diagnostic / biotechnology / Pharmacology (FDA regulated) laboratory experience. The ideal candidate will be a scientifically minded individual, able to read and thoroughly comprehend scientific literature, write scientific protocols and reports following established company guidelines.
TRC Companies, Inc.
$88000 - $124000
San Francisco, California
High capacity for teamwork, creative collaboration, and responsible leadership and delegation; ability to work with individuals of diverse backgrounds and maintain a positive and professional work atmosphere. We recognize that the expertise of our staff is our strongest asset, so we generously reward employees for successful performance and invest in their careers through training and the development of new skills and certifications.
Relay Therapeutics
$115000 - $188000
Cambridge, MA
Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. PhD with at least 5 years or MS with at least 8 years of relevant biotech and/or pharmaceutical industry experience in medicinal chemistry, with an emphasis on lead optimization in small molecule drug discovery.
Medpace, Inc.
Cincinnati, Ohio
Responsibilities : Perform PK and PK/PD analyses (e.g., NCA analysis); Works closely with Clinical Pharmacologist in the preparation of PK Analysis Plan, PK/PD reports or PK/PD section within the Clinical Study Report (CSR); Collaborate with Biostatistician, Clinical Operations, Bioanalytical Scientist, and the Medical team for the execution and management of Phase I-III studies; and. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Perspective Therapeutics
Coralville, IA
Synthesis of Radiolabeled Compounds: Design, synthesize, and optimize radiolabeling methods of compounds (e.g., PET, SPECT, and alpha emitting isotopes) for use in preclinical and clinical studies. Cross-Functional Collaboration: Work closely with other departments, including Manufacturing, Pharmacology, and Clinical Development, to support the integration of radiochemistry into the drug development process.
TRC Companies, Inc.
$62982 - $80434
Windsor, Connecticut
We recognize that the expertise of our staff is our strongest asset, so we generously reward employees for successful performance and invest in their careers through training and the development of new skills and certifications. TRC has long set the bar for clients who require more than just engineering, combining science with the latest technology to devise innovative solutions that stand the test of time.
TRC Companies, Inc.
$49920 - $75192
Madison, Wisconsin
Prepare and review technical reports, graphics, feasibility studies, work plans, design documents, and construction documents, including geologic and hydrogeologic interpretation from field investigations and sampling, to summarize data, results, and remedial options. This position would be part of an experienced team that works closely with Project Managers and other technical leads providing technical support for soil, groundwater, and vapor investigations, due diligence, groundwater monitoring, remediation, and regulatory compliance projects.
TRC Companies, Inc.
$159016 - $180000
Pittsburgh, Pennsylvania
Perform Quality Analysis/Quality Control of deliverables related to projects and tasks managed, as well as projects and tasks managed by others, and are responsible for implementation of the firms' quality procedures at project and task levels. · Interpret geological, hydrogeological, and chemical data from contaminated sites to evaluate and design/optimize soil and groundwater remediation systems, including developing strategy, rationale and cost estimates.
TRC Companies, Inc.
$67288 - $80000
Liverpool, New York
This position will support our Engineering, Construction and Remediation Practice with the completion of environmental investigation and remediation projects, primarily at inactive hazardous waste and petroleum/chemical spill sites. We recognize that the expertise of our staff is our strongest asset, so we generously reward employees for successful performance and invest in their careers through training and the development of new skills and certifications.
TRC Companies, Inc.
$51917 - $75192
Houston, Texas
Demonstrated work experience, or interest in any of the following areas: due diligence/Phase I ESAs, Phase II ESAs, soil and/or groundwater remediation, SWPPP/SPCC preparation, environmental compliance, treatment process design and evaluations, and/or design and implementation of on-site remediation technologies. This position would be part of a very skilled team that works closely with Project Managers and other technical leads providing technical support for site investigation, due diligence, groundwater monitoring, remediation, and regulatory compliance projects.
TRC Companies, Inc.
$103002 - $159120
Greenville, South Carolina
Technical writing Responsibilities also include project management (for simple and complex field sampling, data evaluation and report generation activities (commonly under the RCRA or CERCLA [or similar state programs] regulatory umbrella). Must have 10 - 15 years of professional experience in environmental consulting with progressive project management and technical experience for moderate to complex site investigation/remediation projects under CERCLA, RCRA and state programs.
Bristol Myers Squibb
$156180 - $189252
Cambridge Crossing, MA
Hands-on experience using various cell line and PDX mouse models, humanized mouse models, admixture xenografts, orthotopic models to execute in vivo workflows enabling candidate selection for early clinical development is highly desired. Working closely with project teams and key stakeholders, lead the development of in vivo strategies from target concept to Proof of Concept in patients, applying scientific and technical skills and functional knowledge to complex projects.
Bristol Myers Squibb
$93230 - $112970
San Diego, CA
As an integral part of discovery programs, the group supports lead identification through in vivo model screening and mechanism-of-action studies, develops and validates animal disease models, identifies pathway biomarkers, and establishes clinically relevant endpoints to assess efficacy. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
TechDigital Corporation
Miami, FL
The incumbent performs experiments as defined and planned by supervisor; reviews test results for experimental error and determines if repeats are required; participates in planning studies for the development, evaluation and optimization of assay(s); maintains well organized laboratory notebooks in compliance with relevant procedures; and supports post-launch to resolve performance and/or quality issues. The Development Scientist will participate in planning studies for development, optimization, and failure investigations of protein assay(s); maintain well organized laboratory notebooks in compliance with relevant procedures, and support post-launch (MRB) to resolve performance and/or quality issues for our protein/serology immunoassay chemistries.
TechDigital Corporation
Brea, CA
Familiarity with BCI Clinical Chemistry and/or Immunochemistry Diagnostics platforms a plus (DxC, AU, Access, DxI, IMMAGE)Start Time:12:00 AMHours:Location:Brea 250 South Kraemer Blvd Brea CA 92821 United StatesEducation:Additional Job Details:**** Max Bill Rate $35.00 *** Experience with automated General Chemistry and/or Immunochemistry diagnostic systems preferred. Description/Comment:The Development Scientist I participates in the integration, verification and validation of new and/or improved hardware and software features for Beckman Coulter's Clinical Chemistry and Immunochemistry Diagnostic Systems.
TechDigital Corporation
Brea, CA
The Development Scientist I participates in the integration, verification and validation of new and/or improved hardware and software features for Beckman Coulter's Clinical Chemistry and Immunochemistry Diagnostic Systems. - Maintains well organized laboratory notebooks in compliance with relevant procedures and supports technologies post-launch to resolve performance and/or quality issues.
Alloy Therapeutics
Waltham, MA
You will report to the Associate Director, In Vitro Pharmacology and will work collaboratively in a matrixed environment to drive biologics discovery while supporting rapid decision-making in a fast-moving biotech setting. Execute cell-based functional assays using high-throughput approaches in primary cells, immortalized reporter cell lines, and other disease-relevant cellular systems.
United Therapeutics
Research Triangle Park, NC
Demonstrated understanding of the overall drug development process with clinical trial design, study implementation, sponsor/site interactions, external committee management (DMC, Steering Committees), scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies to be reviewed by health authorities. The Clinical Drug Development Scientist will assist with the coordination, management and execution of Phase I through Phase IV clinical studies and support the conduct of preclinical studies to ensure the successful submission and approval of a drug product by regulatory agencies.
Bristol Myers Squibb
$181930 - $220500
Cambridge, MA
Work-life programs include paid national holidays and optional holidays, Global Shutdown days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Gummi World
Chandler, AZ
Must have advanced knowledge in more than one of the aforementioned formats (Confectionary, starch & starchless gummies, formulations, Capsules, powders etc.) is required as well as having a proven track record developing clean (i.e. short ingredient list) and delicious food that meet specific requirements on a large scale. Must have excellent analytical, written, and organizational skills with the ability to manage complex technical information and have an industry-leading understanding of ingredient functionality, product evaluation, health and nutrition, food manufacturing processes, microbiology, quality assurance principles, and market research practices.
CEDENT
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2. Proficient with electronic systems, including but not limited to enterprise resource planning (ERP), and Microsoft Office applications, particularly Word, Excel, PowerPoint and Project. 3. Associates degree in a scientific discipline and 6+ years’ experience in a pharma industry, formulation and aseptic manufacturing experience required
TechDigital Corporation
Southport, CA
Description/Comment:The Senior Development Scientist leads and/or participates in the planning and execution of studies in the formulation of multiple antimicrobial assays in collaboration with diverse groups within R&D as well as cross-functional teams. The incumbent is responsible for assessing performance of current assay formulations, proposing modifications to the formulation(s) to improve performance, and designing experiments to evaluate the proposed formulations.
Werfen
Norcross, Georgia
The Assay Development Scientist III Performs a variety of tasks, including supervisory activities, associated with the development of new products and new manufacturing process-es, the investigation into and implementation of product and process changes, and the transfer of new products and processes to the manufacturing departments. Oversees and provides leadership to cross functional development team in developing new products using Design Controls.