Top 71 Dir pharmacology Jobs

Director Clinical Pharmacology
The Staffing Resource Group, Inc —Miami, FL
- Up to $110 an hour
- Contract
- Office
- 8 years
- Analysis skills
Quick Apply
13d
Associate Scientific Director, Clinical Pharmacology
Biogen —Remote
- $144,000 - $240,000 a year
- Full-time
- 5 years
- Doctor of Philosophy
- Senior level
- Paid parental leave
- Employee stock purchase plan
Director, Clinical Pharmacology
Arcus Biosciences —Remote
- $245,000 - $260,000 a year
- Weekends as needed
- Office
- Travel
- Conflict management
Pri Sci/Sr Pri Sci/Assoc Director - In Vivo Pharmacology
Think Bioscience —Boulder, CO
- $120,000 - $180,000 a year
- Full-time
- 5 years
- Doctor of Philosophy
- Team management
Quick Apply
Director, Clinical Pharmacology
Alkermes, Inc. —Waltham, MA
- Full-time
- Psychiatry
- Office
- Doctor of Philosophy
Associate Director, Discovery Pharmacology
Amylyx Pharmaceuticals —Cambridge, MA
- $186,000 - $209,000 a year
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
6d
Associate Director, Clinical Pharmacology
AbbVie —Waltham, MA
- $141,500 - $268,500 a year
- Full-time
- Hybrid work
- Master's degree
- Business development experience
- Bachelor's degree
- Paid holidays
- Health insurance
Director/Senior Director, Preclinical Pharmacology/Toxicology
Viking Therapeutics, Inc. —San Diego, CA
- $205,000 - $220,000 a year
- Writing skills
- Doctor of Philosophy
- Mentoring
Quick Apply
Associate Director, Quantitative Clinical Pharmacology
Sarepta Therapeutics —Cambridge, MA
- $160,800 - $201,000 a year
- Full-time
- Hybrid work
- 5 years
- Analysis skills
- Doctor of Philosophy
Senior Director, Quantitative & Clinical Pharmacology
Sarepta Therapeutics —Cambridge, MA
- $222,400 - $278,000 a year
- Full-time
- Hybrid work
- Doctor of Philosophy
- Mentoring
- US work authorization
Associate Director/Director, Clinical Pharmacology
Oruka Therapeutics —Waltham, MA
- $182,000 - $240,000 a year
- 5 years
- Master's degree
- Business development experience
Associate Director, Quantitative System Pharmacology
Viridian Therapeutics, Inc. —Waltham, MA
- $163,000 - $200,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Office
- Paid parental leave
- AD&D insurance
Quick Apply
14d
SENIOR DIRECTOR, DEVELOPMENT PHARMACOLOGY & TOXICOLOGY
Intellia Therapeutics —Cambridge, MA
- $272,538 - $333,102 a year
- 7 years
- Microsoft Excel
- Bachelor of Science
- Free parking
- Commuter assistance
Director, Clinical Pharmacology
AbbVie —North Chicago, IL
- $160,500 - $305,000 a year
- Full-time
- Hybrid work
- 7 years
- Bachelor of Science
- Bachelor's degree
- Paid holidays
- Health insurance
Director, Clinical Pharmacology
Allucent —Cary, NC
- Full-time
- Hybrid work
- English
- 8 years
- Analysis skills
- Flexible schedule
- Referral program
Quick Apply
Director, Clinical Pharmacology
IMMUNEERING CORPORATION —New York, NY
- $190,000 - $240,000 a year
- Full-time
- Office
- Doctor of Philosophy
- Quality control
Quick Apply
Director, Clinical Pharmacology
Fore Biotherapeutics US Inc —Philadelphia, PA
- $205,000 - $250,000 a year
- Full-time
- 8 years
- Analysis skills
- Doctor of Philosophy
Senior Director, Quantitative Pharmacology
Sun Pharmaceutical Industries, Inc (USA) —Princeton, NJ
- $215,500 - $239,500 a year
- Computer Science
- 5 years
- Writing skills
- Disability insurance
- Health insurance
Senior Director, Oncology Pharmacology
Jazz Pharmaceuticals —California
- $232,000 - $348,000 a year
- Analysis skills
- Doctor of Philosophy
- Mentoring
- Health insurance
- Dental insurance
Director/Senior Director, In Vivo Pharmacology
Rezo Therapeutics —San Francisco, CA
- $195,000 - $290,000 a year
- Full-time
- Doctor of Philosophy
- Team management
- Quality control
- Commuter assistance
- Health insurance
Quick Apply

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Director Clinical Pharmacology

The Staffing Resource Group, Inc -
Miami, FL

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Job Details

Contract
Up to $110 an hour
13 days ago

Qualifications

Optimizing workflow processes
FDA submissions
Technical writing for researchers
Medical writing
ICH guidelines
Doctor of Philosophy
Pharmaceutical company experience
Managing clinical research teams
Leading team collaboration initiatives
Communication with regulatory authorities for clinical trials
Project leadership
Cross-functional team management
Pharmaceutical research experience
Cross-functional communication

Full Job Description

Director, Clinical Pharmacology

Location: Jersey City, New Jersey
Industry: Pharmaceutical
Hours: M-F, 8am-5pm, hybrid (2 days in office, 3 remote)
Hourly rate: Up to $110-$115/hr.
Employment Type: Contract with the opportunity to go permanently based on performance and business needs.

Environment:
Our client is a dynamic specialty pharmaceutical company engaged in the research, development, manufacture, marketing, and sale of prescription pharmaceutical products. They are a leading developer of advanced transdermal drug delivery technologies and prescription transdermal products.

Overview:
The Director, Clinical Pharmacology provides strategic scientific and technical leadership across all aspects of Clinical Pharmacology and model-informed drug development, including study strategy, pharmacokinetic (PK) and PK/PD analysis, modeling and simulation, and regulatory submissions to support early- and late-stage clinical development.
This role serves as a key cross-functional leader with regulatory affairs, clinical operations, clinical research project management, data management, biostatistics, and external partners to ensure clinical pharmacology strategies and deliverables are aligned with corporate objectives, regulatory expectations and internal standard operating procedures (SOPs). The Director leads the interpretation and integration of clinical pharmacology data into development decisions and provides strategic input into regulatory interactions with Agencies including the U.S. Food and Drug Administration (FDA). This position reports directly to the Head of Clinical and Regulatory Affairs and serves as a strategic clinical pharmacology leader within the development organization.
The Director is expected to independently lead complex development programs, influence program and portfolio strategy and contribute to organizational initiatives process improvements and scientific innovation within Clinical Pharmacology.

Responsibilities:

Provide strategic clinical pharmacology and pharmacometrics leadership to cross-functional development teams and guide the design, execution, and interpretation of clinical pharmacology studies across multiple development programs.
Lead dose selection and optimization, dosing regimens (including special populations), and provide scientific oversight for study design in collaboration with pharmacometrics, biostatistics, and clinical colleagues.
Oversee and/or conduct non-compartmental and compartmental analyses of clinical PK data and interpret PK and PK/PD results. Ensure the use of validated bioanalytical methods for drug and biomarker measurement. Experience with WinNonlin is required.
Lead collaborations with external bioanalytical laboratories, CROs, consultants, and partner organizations to ensure high-quality and timely execution of clinical pharmacology deliverables including review and approval bioanalytical validation reports and study outputs.
Provide strategic oversight of modeling and simulation activities, including population PK, PK/PD modeling, and clinical trial simulations, to support dose selection and study design, labeling strategies and regulatory submissions. Experience with NONMEM/R is preferred.
Develop and drive clinical pharmacology and pharmacometrics strategies that support scientific, regulatory, and commercial objectives across assigned programs and contribute to portfolio-level decision-making.
Serve as the clinical pharmacology subject matter expert in regulatory interactions and lead the preparation, review, and approval of regulatory documents, including clinical study reports, protocols, investigator brochures, briefing books, IND/NDA/BLA submission content, responses to regulatory questions, presentations, abstracts, and other scientific materials.
Maintain awareness of emerging scientific literature, regulatory guidance, and advances in clinical pharmacology and pharmacometrics, incorporating innovative approaches into study design and life-cycle management strategies where appropriate.
Support the evaluation of compounds proposed for incorporation into transdermal systems or other formulations. Experience with transdermal drug development is preferred but not required.
Contribute scientific and strategic expertise to business development and cross-functional teams in the scientific assessment of potential in-licensing opportunities.
Mentor and provide scientific leadership to junior staff and cross functional team member, fostering technical development and promoting excellence within the Clinical Pharmacology function.

Qualifications

Ph.D. in Pharmaceutical Sciences, Pharmacokinetics, Clinical Pharmacology, or a related discipline.
Minimum of 8-10 years of relevant experience in clinical pharmacology and/or pharmacometrics within a pharmaceutical or biotechnology R&D environment including demonstrated leadership of clinical development programs
Strong working knowledge of FDA, ICH, and CFR regulations and clinical pharmacology-related guidance documents.
Demonstrated experience supporting regulatory submissions and interactions for development-stage programs.
Demonstrated scientific leadership and ability to influence to cross-functional teams and development strategy in a matrixed environment.
Strong analytical, strategic thinking, problem-solving, and scientific writing skills.
Proven ability to independently lead complex programs and drive clinical pharmacology data-driver decisions with significant development and regulatory impact.
Effective collaborator with the ability to build relationships across internal and external teams, business partners, and senior leadership.
Experience monitoring scientists and contribution to organizational capability development.
Applies expert scientific judgment to complex clinical pharmacology and pharmacometric challenges with significant program impact.
Leads strategic recommendations influencing study design, dose selection, regulatory strategy and development planning.
Identifies opportunities for improved methodologies, modeling approaches, and operational efficiencies to advance clinical pharmacology capabilities and program execution.

ADA/EOE
IND123

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