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Associate Director – Clinical Pharmacology Lead

Job in Ridgefield, Fairfield County, Connecticut, 06877, USA
Listing for: Jobtailor
Full Time position
Listed on 2026-08-16
Job specializations:
  • Pharmaceutical
    Medical Science Liaison
  • Healthcare
    Medical Science Liaison, Medical Science, Clinical Research
Salary/Wage Range or Industry Benchmark: 150000 - 210000 USD Yearly USD 150000.00 210000.00 YEAR
Job Description & How to Apply Below

Support the clinical development of new drugs and further development of approved drugs with emphasis on the design and execution of the Clinical Pharmacology development strategy
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.
Acts as Clin Pharm representative in trial and project teams and regulatory meetings
Drive science and innovation through continuous evaluation and implementation of new methods and strategies around Clinical Pharmacology.
Contributes to the Clin Pharm section of official documents and engages with regulatory agencies on matters pertaining to CP during drug development.

Requirements
  • Doctoral degree (MD or PhD) in Medicine, Pharmaceutical Sciences or CP and prior experience in the pharmaceutical industry, regulatory agencies, or academia preferred OR
  • Master’s degree in Medicine, Pharmaceutics, CP, or equivalent area of focus with at least three to five (3-5) years of relevant experience in CP in the pharmaceutical industry, regulatory agencies, or academia could be considered for this position.
  • Experience using NONMEM software in industry setting
  • Excellent communication (both written and verbal) and presentation skills
  • Mindful of local, global, internal, and external cultures to ensure that messages are received positively and effectively.
  • Evidence of strong teamwork, also in global and remote context.
  • Good interpersonal skills with the ability to interact effectively with people, internally and externally (e.g., CROs, experts, management).
Core Competencies

Demonstrates expertise in Clinical Pharmacology development strategies, regulatory engagement, and scientific documentation. Proven ability to drive innovation and collaboration in drug development within diverse teams and settings.

Highest-signal resume keywords
  • Clinical Pharmacology Development
  • NONMEM Software Experience
  • Regulatory Agency Engagement
  • Excellent Communication Skills
  • Teamwork in Global Context
ATS Optimization Keywords Hard Skills
  • Clinical Pharmacology
  • Drug Development
  • Scientific Documentation
  • Pharmaceutical Sciences
  • Medicine
  • Pharmaceutics
  • Regulatory Compliance
  • Data Analysis
  • Clinical Trial Design
  • Pharmaceutical Industry Experience
Soft Skills
  • Interpersonal Skills
  • Presentation Skills
  • Cultural Awareness
  • Team Collaboration
  • Effective Communication
Certifications & Qualifications
  • Doctoral Degree (MD or PhD)
  • Master’s Degree in Medicine or Pharmaceutics
Industry Keywords
  • Pharmaceutical Industry
  • Regulatory Agencies
  • Clinical Trials
  • Drug Registration
  • Scientific Concepts
Tools & Technologies
  • NONMEM Software
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Position Requirements
10+ Years work experience
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