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- Tasks: Lead non-clinical PKPD studies and collaborate with project teams to ensure quality data.
- Company: Join a global biopharmaceutical company dedicated to improving lives through innovative treatments.
- Benefits: Competitive pay, flexible hours, and the chance to work on impactful projects.
- Why this job: Be at the forefront of drug development in a supportive and collaborative environment.
- Qualifications: PhD/MSc/BSc in relevant fields with 5+ years of PKPD experience required.
- Other info: Location: Slough; must have UK work entitlement and may require DBS check.
Principal Scientist PKPD CK Group•Slough, Berkshire
Principal Scientist PKPD
CK Group are recruiting for a Principal Scientist PKPD to join a global pharmaceutical company on a contract basis initially for 12 months.
£35.20 Per hour (PAYE) / £47.92 (Umbrella) – flexible for experienced candidates.
Principal Scientist PKPD Role:
- Participate in the development of non-clinical PKPD and GLP toxicokinetics studies. Lead the non-clinical PKPD strategy. Participate in protocol designs and writing by providing scientific support and input into regulatory study designs and protocols.
- Work collaboratively with the project teams representatives (e.g. Non-Clinical Safety, Bioanalysis, Clinical Pharmacology) and with the CROs, to ensure high quality data is generated.
- Deliver PKPD study reports and integrated summaries of the studies and participate in regulatory submission documents.
- Facilitate the advancement of drug candidates by building a thorough knowledge of the drug pharmacology and PKPD.
- Work collaboratively with the project teams representatives (e.g. Non-Clinical Safety, Bioanalysis, Clinical Pharmacology) and with the CROs, to ensure high quality data is generated
Principal Scientist PKPD
CK Group are recruiting for a Principal Scientist PKPD to join a global pharmaceutical company on a contract basis initially for 12 months.
Salary:
£35.20 Per hour (PAYE) / £47.92 (Umbrella) – flexible for experienced candidates.
Principal Scientist PKPD Role:
- Participate in the development of non-clinical PKPD and GLP toxicokinetics studies. Lead the non-clinical PKPD strategy. Participate in protocol designs and writing by providing scientific support and input into regulatory study designs and protocols.
- Work collaboratively with the project teams representatives (e.g. Non-Clinical Safety, Bioanalysis, Clinical Pharmacology) and with the CROs, to ensure high quality data is generated.
- Deliver PKPD study reports and integrated summaries of the studies and participate in regulatory submission documents.
- Facilitate the advancement of drug candidates by building a thorough knowledge of the drug pharmacology and PKPD.
- Work collaboratively with the project teams representatives (e.g. Non-Clinical Safety, Bioanalysis, Clinical Pharmacology) and with the CROs, to ensure high quality data is generated
Your Background:
- Experience working in a matrix environment, to help design and set non-clinical PKPD study protocols, and analyze, interpret, and report PKPD results including GLP toxicokinetics studies.
- PhD/MSc/BSc relevant discipline (quantitative pharmacology; pharmacokinetics /pharmacodynamics; DMPK, etc.) with more than 5 years hands on experience in PKPD data analysis within a pharma company or CRO environment.
- Good understanding of pharmacology and pharmacologic processes related to disease and drug mechanisms.
- Hands-on experience in delivering high quality pre-clinical PKPD data analysis. Proficiency in the use of Phoenix- WinNonlin for PKPD analysis is essential. Use of other modelling and simulation packages and tools, such as Berkeley Madonna and/or R would be advantageous.
- Good written and verbal communication skills, and ability to communicate study results and produce high standard reports that meet regulatory submission standards. Record of publications and other external scientific contributions relevant to PKPD will be a plus.
Company:
Our client is a is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future.
Location:
This role is based at our client’s site in Slough.
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Principal Scientist PKPD employer: CK Group
Contact Detail:
CK Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Scientist PKPD
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who have experience in PKPD. Attend relevant conferences or webinars to meet potential colleagues and learn about the latest trends in pharmacokinetics and pharmacodynamics.
✨Tip Number 2
Familiarise yourself with the specific tools mentioned in the job description, such as Phoenix-WinNonlin and other modelling packages. Consider taking online courses or tutorials to enhance your proficiency, as this will demonstrate your commitment and readiness for the role.
✨Tip Number 3
Prepare to discuss your previous experiences in a matrix environment during the interview. Think of specific examples where you successfully collaborated with cross-functional teams to deliver high-quality data and how you contributed to study protocols.
✨Tip Number 4
Stay updated on recent publications and advancements in PKPD and GLP toxicokinetics. Being knowledgeable about current research can help you engage in meaningful discussions during interviews and showcase your passion for the field.
We think you need these skills to ace Principal Scientist PKPD
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in PKPD and GLP toxicokinetics studies. Emphasise your hands-on experience and any specific tools you've used, like Phoenix-WinNonlin.
Craft a Strong Cover Letter: Write a cover letter that clearly outlines your understanding of the role and how your background aligns with the company's needs. Mention your collaborative experience with project teams and CROs.
Highlight Key Skills: In your application, focus on your communication skills and ability to produce high-quality reports. Provide examples of your previous work that demonstrate these abilities.
Proofread Your Application: Before submitting, carefully proofread your application for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial in this field.
How to prepare for a job interview at CK Group
✨Showcase Your Technical Expertise
Make sure to highlight your hands-on experience in PKPD data analysis and your proficiency with tools like Phoenix-WinNonlin. Be prepared to discuss specific projects where you successfully applied these skills.
✨Demonstrate Collaborative Skills
Since the role involves working with various project teams and CROs, share examples of how you've effectively collaborated in a matrix environment. Emphasise your ability to communicate and work well with cross-functional teams.
✨Prepare for Regulatory Discussions
Familiarise yourself with regulatory submission standards and be ready to discuss your experience in writing study protocols and reports. This will show that you understand the importance of compliance in the pharmaceutical industry.
✨Highlight Your Research Contributions
If you have publications or other scientific contributions related to PKPD, make sure to mention them. This demonstrates your commitment to the field and can set you apart from other candidates.
