Celerion

Pharmacokinetic Scientist

Celerion  •  Canada (Remote)  •  15 days ago
Apply
Save Job
Mark Applied Mark Interviewed Mark Offered
Hide Job Report Job
AI can make mistakes so check important info. Chat history is never stored.
44
AI Success™

Job Description

We are looking for a full-time  Pharmacokinetic Scientist to join our Clinical Pharmacology team.  This role may be based at either our Lincoln, NE, or Montreal, Canada facilities.  Remote working relationships may be considered based upon experience.   The Pharmacokinetic Scientist will assist with pharmacokinetic data analysis, scientific interpretation of study results, clinical report writing, and interactions with clients.

Essential Functions

  • Data analysis and interpretation
  • Perform PK analyses independently
  • Assist with PD analyses
  • Interpret PK and statistical results and findings independently
  • Perform QC reviews as assigned
  • Write and review reports as assigned
  • Prepare PK data/report files for electronic filing of projects for submission to regulatory agencies
  • Maintain and file all supportive documentation pertaining to the study and ensure proper archiving of projects
  • Other responsibilities
  •  Interact with clients alongside or under direction of a senior scientist, as needed
  • Prepare internal presentations

Requirements

  • Master’s or PhD degree in a biology-focused sciences related field with 2+ years of related experience required
  • Competence in performing noncompartmental pharmacokinetic analysis with software applications such as Phoenix WinNonlin
  • Familiarity with processes and applications related to non-linear mixed-effect modeling and/or physiologically-based pharmacokinetic modeling is an asset
  • Excellent oral and written skills (English language) required
Celerion

About Celerion

Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines.

With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings.

Our operations are strategically located in:

Lincoln, Nebraska (Corporate Headquarters)

Philadelphia, Pennsylvania

Phoenix, Arizona

Belfast, Northern Ireland,UK

Zurich, Switzerland

Vienna, Austria

Richmond, Virginia

Montreal, Quebec, Canada

For more information, visit: www.celerion.com

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Lincoln, NE
Year Founded
2010
Website
celerion.com
Social Media