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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

Requirements:

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. 

 


Position:

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.

 

 

 Qualifications:

  • 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.

 

Keywords:

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
England
Tel:  01293 584 300
Fax:  01293 534 133
Website:  Visit Our Web Site

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