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Job Details

Director / Senior Director, Clinical Pharmacology - USA

Company: RBW Consulting
Location: New Jersey, USA
Reference: IKSDCP-6271
Closing Date: 25 Jul 18
Type: Full Time
Salary (£): Competitive
Benefits: Highly Competitive Package offered

Job Summary:

Global Pharma seeks expert scientist with capability to confidently take on high level strategic oversight - based in New Jersey


Director / Senior Director, Clinical Pharmacology


Are you an experienced Clinical Pharmacologist with a strong command of quantitative modelling, and pharmacometrics? I am currently working with a market leading, global pharma currently seeking expansion within their Clinical Pharmacology strategic team. You will be taking on key responsibilities whilst working within a strong scientific pipeline. This position will be based in New Jersey. 



As a Senior / Director, Clinical Pharmacology you will:

  • Apply your Clinical Pharmacology expertise to the ongoing drug development within a range of key therapeutic areas, including both small molecules and biologics.
  • Lead the Clinical Pharmacology component of the Clinical Development Plan
  • Design and interpret studies within early, full and life cycle stages of development.  
  • Develop and implement an effective quantitative strategy, to ensure of appropriate PKPD analysis. 
  • Provide contributions to Clinical Pharmacology strategy within both early and late stage projects, and be responsible for the design and execution of Clinical Pharmacology and modelling and simulation plans.
  • Contribute to the preclinical aspects within studies, ensuring the quantitative mechanistic knowledge is sound, and supports human application.
  • Provide subject matter expertise within cross functional teams, alongside health authority interactions and regulatory submissions. Collaborate with colleagues to provide quantitative pharmacology support within First-in-human dose selection and study design.




  • A PhD or PharmD within a relevant discipline
  • Various levels of experience will be considered, and a minimum of 7+ year’s post-educational experience would be required.
  • Strong experience within Clinical Pharmacology, alongside hands-on knowledge of PK and PKPD modelling, using a range of software, such as NonMem, Monolix and R etc.
  • Demonstrated leadership skills are desired.
  • Experience handling submission reports within regulatory documents, and handling responses to health authorities.


I manage a range of other permanent and freelance positions for a broad portfolio of clients (Biotech, CRO and Pharma). If the above role isn’t for you but you’d nevertheless like to discuss your options in the market, I’d welcome a confidential discussion by phone or email. Contact Ian Kulka at (617) 982 1238.



Clinical Pharmacology, Protocol design, submission, Pharmacometric, Leader, Modelling, Nonlinear, pharmacometry, simulation, systems, Biology, biological, pathways, mechanism, pharmacokinetics, pharmacodynamics, Clinical, NonMEM, R, Monolix, PKPD, PK/PD, “Pop PK”, modeller, strategy, strategic, Directorial, leader, quantitative

Apply for this job: Director / Senior Director, Clinical Pharmacology - USA

Contact Information:

Address:  Head Office
Origin Two 106 High Street, Crawley RH10 1BF
RH10 1BF
Tel:  01293 584 300
Fax:  01293 534 133
Website:  Visit Our Web Site

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