Pharmacologist Jobs in the United States
Care Career
$2560
Dayton, MN
A pharmacologist works with hospitals, biopharmaceutical companies and other organizations to discover and develop therapies to treat cancer and various other diseases. They often collaborate with research scientists in various clinical development programs to conduct quantitative modeling, clinical trial simulations, and safety tests.
Joulé
$150000 - $170000
Parsippany, NJ
Prepare and review clinical pharmacology content for key clinical and regulatory documents, including clinical study reports, regulatory submission modules, and briefing materials (e.g., FDA briefing books) . System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.
System One
$150000 - $165000
Parsippany, New Jersey
Prepare and review clinical pharmacology content for key clinical and regulatory documents, including clinical study reports, regulatory submission modules, and briefing materials (e.g., FDA briefing books) . System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.
Cytel
Olympia, WA
Position Overview:** Our Principal Pharmacometricians provide advanced analytical and development support and influence for the associated client's trials providing expertise into processes, regulatory strategy, modeling, as well as potentially providing oversight of work supported by other vendors. + Review and contribute to study reports and quantitative clinical pharmacology l sections of regulatory submission dossiers, lead electronic submissions of clinical data to regulatory authorities, and participate to meetings with regulatory authorities.
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.
Merck
$129000 - $203100
Olympia, WA
Required Experience:** + Experience in developing mechanistic PK-PD models and QSP models for decision making in early and/or late-stage clinical development + Experience with mechanistic modeling for antibody drug conjugates (ADCs), bispecifics, and/ or T-cell engagers will be preferred + Experience with modeling and simulation packages or programming languages (e.g., MATLAB/SimBiology, QSP Designer, R) + Hands on experience building, calibrating, and validating QSP models + Professional working proficiency in written and verbal communication. + Bringing forward combination drug approaches by leveraging QSP models to design and prioritize combination clinical trials + Work in close collaboration with biologists, clinicians, clinical pharmacologists, pharmacometricians and other line functions to improve our understanding of disease mechanisms and modalities + Experience with QSP modeling in oncology for different modalities (small molecules,monoclonal antibodies, antibody drug conjugates, T-cell engagers, bispecifics).
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.
CellCarta
Naperville, IL
Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. As an Assay Development Scientist within our Genomics Services team, you will be responsible for the implementation, development, and validation of high-quality qPCR, dPCR, and NGS assays for use in clinical trials, utilizing state-of-the-art RNA and DNA technologies.
Lancesoft
$1
Englewood Cliffs, NJ
In developing solutions, you drive functional excellence whilst effectively combining the relevant culinary, nutritional, technical, and market knowledge to design products for consumers / customer needs. Your deep knowledge of the technologies and available capabilities in-house and at the external manufacturing network, combined with your curiosity about solving consumer problems, will result in bringing the right solutions to the markets.
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.
Pfizer
$176600 - $294300
Bothell, WA
Provides clinical support to the study team or clinical program in response to audits or inspections, including providing support as needed to audit/inspection **BASIC QUALIFICATIONS** + Advanced degree or professional certification in a health care related, scientific or technical discipline required + Years of experience in biopharmaceutical industry in clinical research and development: + BA/BS with 8+ years of experience + MBA/MS with 7+ years of experience + PhD/PharmD with 5+ years of experience + Clinical research experience in phase 3/pivotal space + Extensive knowledge of clinical development, global and regional regulation, ICH/GCP, adverse event management + Demonstrated clinical, administrative, and project management capabilities, as well as excellent verbal and written communication skills in English, in relating to individuals both inside and outside Pfizer + Demonstrated experience establishing, managing, and training teams in clinical development + Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. The **Clinical Development Scientist (Director)** ensures scientific integrity and participant safety in clinical trials, designs and executes high-quality studies, maintains compliance, manages risks and emerging clinical issues, and supports interpretation and communication of clinical data.
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. .
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.
Azalea Therapeutics, Inc.
$115000 - $140000
Berkeley, CA
Fraudulent emails claiming to be sent by Azalea or Azalea employees may come from similar sounding emails with endings like “@azaleajobs.com” or “@azalea.com” or even emails ending in common public domain addresses with endings like “@gmail.com,” There can also be instances of fraudulent communication that use the names and pictures of known company employees claiming to be sent from those employees, or that even link out to fake websites that were created to look and feel like the real company website.
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.
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.
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.
$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.
$58593.6 - $85280
Manassas, Virginia
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. 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.
TRC Companies, Inc.
$65686.4 - $112673.6
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.
$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.
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.
SQA Solution
$45 - $47
Oro Valley, Arizona
Initiate, direct, and execute scientific research, product early development, and manufacturing process strategies to support new and existing products. Ensure complete and accurate laboratory documentation and electronic files, and adhere to company policies for GMP, GLP, and Design Control.
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.
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. As Alloy Tx enters its next phase of growth, we are expanding our capabilities to include mechanistic studies that enhance preclinical development and further advance our translational research efforts.
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.
AlliedTravelCareers
$2866
Washington, IA
A pharmacologist works with hospitals, biopharmaceutical companies and other organizations to discover and develop therapies to treat cancer and various other diseases. They often collaborate with research scientists in various clinical development programs to conduct quantitative modeling, clinical trial simulations, and safety tests.
AlliedTravelCareers
$3234
Pittsfield, MA
A pharmacologist works with hospitals, biopharmaceutical companies and other organizations to discover and develop therapies to treat cancer and various other diseases. They often collaborate with research scientists in various clinical development programs to conduct quantitative modeling, clinical trial simulations, and safety tests.
AlliedTravelCareers
$2560
Dayton, MN
A pharmacologist works with hospitals, biopharmaceutical companies and other organizations to discover and develop therapies to treat cancer and various other diseases. They often collaborate with research scientists in various clinical development programs to conduct quantitative modeling, clinical trial simulations, and safety tests.
DeepCure
$170000 - $210000
Boston, MA
In this role, you will serve as a scientific leader driving early-stage drug discovery programs with a strong emphasis on immunology-driven biology and pharmacology, from target validation through IND-enabling stages. By combining advanced computational platforms with deep biological and chemical expertise, DeepCure aims to deliver differentiated therapeutic candidates faster and more efficiently.
Star Therapeutics
$156000 - $195000
South San Francisco, CA
As an Associate Director, the candidate is expected to represent translational sciences as a translational medicine lead for clinical studies and work closely with the clinical development team members including bioanalysis, clinical operations, regulatory affairs, quality, medical writing, safety, clinical research and clinical leadership. As part of the collaborative research team role, the candidate is expected to work with individuals across research and translational research groups, including discovery research, drug development and protein sciences, preclinical bioanalysis and other junior staff within translational research organization.
MetaOption, LLC
Ayer, MA
You will develop and optimize medical nutrition beverage and powder formulations using food science expertise while supporting clinical evidence, ingredient initiatives, IP protection, and GMP and food safety compliance. Skills: scientist, Food Science, Nutrition, product development experience from concept to commercialization in nutrition, food, beverage, supplement, nutraceutical, or biotech industries.
TechDigital
Brea, CA
Start Time:12:00 AMHours:Location:Brea 250 South Kraemer Blvd Brea CA 92821 United StatesEducation:Additional Job Details:***MAX BILL RATE $35*** Experience with automated General Chemistry and/or Immunochemistry diagnostic systems preferred, Familiarity with BCI Clinical Chemistry and/or Immunochemistry Diagnostics platforms a plus (DxC, AU, Access, DxI, IMMAGE) 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
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
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.
Nature's Sunshine Products
Lehi, UT
This is a highly collaborative role ideal for candidates looking to build strong technical formulation skills, gain exposure to the full product development lifecycle, and grow within a cross-functional product organization. Partner with the Label Coordinator, Regulatory, and Marketing to ensure product labels accurately reflect the formulation, specifications, and overall product design.
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.
Care Career
$3234
Pittsfield, MA
A pharmacologist works with hospitals, biopharmaceutical companies and other organizations to discover and develop therapies to treat cancer and various other diseases. They often collaborate with research scientists in various clinical development programs to conduct quantitative modeling, clinical trial simulations, and safety tests.
Care Career
$2866
Washington, IA
A pharmacologist works with hospitals, biopharmaceutical companies and other organizations to discover and develop therapies to treat cancer and various other diseases. They often collaborate with research scientists in various clinical development programs to conduct quantitative modeling, clinical trial simulations, and safety tests.
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
Boehringer Ingelheim
$75000 - $122000
Ridgefield, CT
The successful candidate will develop and execute in vivo and ex vivo murine experiments in support of company drug discovery goals in an independent manner with thoughtful trouble shooting. The in vivo Oncology Pharmacology group is seeking a highly motivated, organized, interactive, team-oriented Scientist II to join our Ridgefield, CT team .
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.
Pfizer
$176600 - $282900
Seattle, WA
Follow relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures; leads or actively participates in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures; may be a subject matter expert or business process owner for a relevant SOP or procedure. both as a leader and a key contributor Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
Vertex Pharmaceuticals
$59 - $71
Seattle WA/Onsite, undefined
Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners. This position plays a critical role in analytical method execution, data review, and cross-functional CMC collaboration, supporting early-phase clinical development for protein therapeutics.
Wheeler Bio, Inc.
Oklahoma City, OK
PhD degree with no prior experience or Master’s Degree (in biochemistry, chemistry, microbiology, or other life-science discipline) with at least 2 years of relevant experience will be given consideration. Position Overview: Wheeler Bio is seeking a motivated analytical mind with a passion for problem solving, fast-paced environments, and expertise in protein mass spectrometry to join the analytical team.