Senior Pharmacokineticist
Senior Pharmacokineticist
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Job Description
What if your PK expertise was the reason a new drug reached patients faster
Before a drug becomes a treatment it comes through us. Fortrea is one of the largest early-stage clinical research organizations in the world. Our Clinical Pharmacology team delivers the PK and safety insights that shape safety dosing and development decisions transforming molecules into meaningful therapies.
REMOTE JOB UK
We are now seeking our new Senior Pharmacokineticist to join our global Clinical Pharmacology team.
- Full-time this is a home-based job anywhere in the UK.
- 37 hours per week Monday to Friday.
WHAT YOU WILL DO
As a Senior PK Scientist you will go beyond reviewing draft protocols PK reports or performing PK parameters calculation. At this senior level your impact will extend to identifying gaps not only withing individual protocols but also in sponsors broader drug development strategies.
On a typical day you will:
- Shape Study Design. Use your critical eye to advise on sampling schedules or dose-escalation plans. Spot gaps that could compromise PK/PD data quality and recommend changes that optimize data capture for robust insights.
Conduct and review non-compartmental PK or PK/PD analyses calculations with Phoenix WinNonLin ensuring accuracy and scientific rigor.
- Interpret and advise: provide clear insightful interpretation of PK and PK/PD data helping sponsors make confident decisions about dosing safety and next steps.
WHO YOU WILL WORK WITH
Here at Fortrea you will never work in isolation and your contributions will have a global impact:
- You will be part of a diverse collaborative global network of Pharmacokinetic Scientists across EMEA the US Canada and India. Together youll share knowledge challenge ideas and contribute to studies that impact the life of people around the world.
- Day to day you will work closely with Medical Writing Statistics Programming or Project Management bringing your PK expertise to cross-functional teams improving interdepartmental processes and mentoring less experienced team members.
WHO YOU ARE
Required:
- Extensive PK experience in Phase I-III clinical research with healthy volunteers and patients (CRO or biopharma) including study design protocol review PK (/PD) Analysis dose escalation interim analysis data interpretation and input to CSRs.
- Proven track record in non-compartmental analysis with WinNonLin
- Strong project management skills including planning activities meeting timelines and keeping studies on track to key milestones.
- Bachelors degree in Biological Life Sciences Pharmacy or Bioanalytical Chemistry.
Preferred:
- Confidence in client-facing discussions explaining results answering questions and justifying interpretations in data review meetings.
EVERY NEW TREATMENT WILL BEGIN WITH YOU
Here you will belong to a team that generates the early data that turns discovery into possibility and possibility into real therapies for patients.
Join us and support our mission To help make life-changing healthcare solutions possible.
Apply now and be part of an extraordinary journey.
#LI-CV1 #LI-Remote
Learn more about our EEO & Accommodations request here.
Required Experience:
Senior IC
Employment Type
Full-Time
