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Senior Pharmacokinetic Scientist (UK Based)

Celerion Holdings, Inc.

United Kingdom

Remote

GBP 80,000 - 100,000

30+ days ago

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Job summary

An established industry player is seeking a Senior Pharmacokinetic Scientist to join its Clinical Pharmacology team. This exciting remote role in the United Kingdom involves conducting complex pharmacokinetic and pharmacodynamic analyses, providing scientific interpretation of study results, and engaging with clients. You will be responsible for writing clinical reports, preparing regulatory documents, and contributing to the success of the team. If you are passionate about advancing clinical research and want to be part of a company that values integrity, trust, and teamwork, this opportunity is perfect for you.

Qualifications

  • Experience in pharmacokinetic and pharmacodynamic analysis.
  • Strong skills in statistical interpretation and clinical report writing.

Responsibilities

  • Conduct pharmacokinetic data analysis and provide scientific interpretation.
  • Perform clinical report writing and interact with clients independently.

Skills

Pharmacokinetic Analysis

Pharmacodynamic Analysis

Statistical Interpretation

Clinical Report Writing

Staff Management

Education

PhD in Pharmacology or related field

Master's in Pharmacology or related field

Job description

Senior Pharmacokinetic Scientist (UK Based)

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

We are looking for a full-time Senior Pharmacokinetic Scientist to join our Clinical Pharmacology team. This role will be based remotely in the United Kingdom.

The Senior Pharmacokinetic Scientist will conduct pharmacokinetic data analysis, provide scientific interpretation of study results, perform clinical report writing, and independently handle interactions with clients.

Essential Functions:
  1. May be responsible for staff management in accordance with the organization's policies and applicable laws. Responsibilities include interviewing, hiring, and training employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems; development and coaching of employees.
  2. Perform PK analyses independently on a variety of complex studies.
  3. Perform PD analyses independently.
  4. Interpret PK, PD and statistical results and findings independently.
  5. Perform QC reviews as assigned.
  6. Write and review reports as assigned.
  7. Prepare PK/PD data/report files for electronic filing of projects for submission to regulatory agencies.
  8. Maintain and file all supportive documentation pertaining to the study and ensure proper archiving of projects.
  9. Contribute to regulatory documents (e.g. NDA, ANDA).
  10. Perform and/or oversee drafting of pharmacometric analysis plans, perform analyses and write pharmacometric reports.
  11. Represent the client in regulatory interactions or client internal meetings.
  12. Prepare internal presentations.
  13. Interact with internal departments (e.g. bioanalytical, project management, business development, etc.).
  14. Assist in the preparation of clinical pharmacology trial protocols.
  15. Publish manuscripts in PK/PD area.
  16. Lead and/or participate in functions required to ensure the success of department or market segment team.

Celerion Values: Integrity, Trust, Teamwork, Respect.

Celerion is an Equal Opportunity Employer.

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