Pharmacokinetic Scientist

Kymos Group; Barcelona; Presencial; EUR 45.000 - 65.000; Jornada completa

Descripción de la vacante

Kymos Group in Barcelona is seeking a Pharmacokinetic Scientist to join its dynamic team. The role involves acting as a principal investigator, designing pharmacokinetic analyses, and providing expert guidance on ADME and DMPK in drug development.

The ideal candidate must have fluency in Spanish and advanced English, along with strong organizational and analytical skills. Additional competencies include effective communication, stakeholder management, and a focus on quality and compliance.

Responsabilidades

• Act as principal investigator / study director for assigned projects.
• Design and conduct pharmacokinetic analyses for drug development.
• Drive pharmacokinetic analysis using Phoenix WinNonlin.
• Write protocols and reports for drug bioanalysis.
• Analyze and interpret preclinical and clinical PK studies.
• Provide expert ADME and DMPK guidance.
• Follow Good Laboratory Practices and Company SOPs.

Conocimientos

Fluent Spanish

Advanced English

Strong organizational skills

Attention to detail

Analytical mindset

Effective communication

Stakeholder management

Problem-solving skills

Ability to manage multiple priorities

Customer and service orientation

Quality and compliance focus

Descripción del empleo

Due to our recent business expansion and facility growth, we are looking for a Pharmacokinetic Scientist to join our dynamic team.

As ,Pharmacokinetic Scientist your responsibilities will include:

• Act as principal investigator / study director, taking responsibility for assigned projects
• Act as coordinator of pharmacokinetic (PK) activities through all group
• Design, conduct, interpret and summarize pharmacokinetic and pharmacodynamic analyses in support of drug development
• Drive preclinical and clinical pharmacokinetic non-compartmental and compartmental Analysis using Phoenix WinNonlin
• Write protocols and reports covering objectives, methods, analysis and results for drug bioanalysis in different species and biological matrices (plasma/serum/whole blood, urine, faeces, tissue homogenates…)
• Analyse and interpret preclinical and clinical PK studies such as DMPK, ADME, BE/BA, Tox, SAD, MAD) and data to optimize PK plan, sampling and dosing
• Provide expert ADME and DMPK guidance into the non-clinical and clinical studies
• Follow Good Laboratory Practices (GLP) and Good Clinical Practices (GCP), Company Standard Operating Procedures (SOPs) and Sponsor Study protocols
• Support business development and marketing activities, foster client relationships and help new clients onboard
• Attend meetings with Sponsor to explain PK results of the studies
• Stay tuned in with the latest PK developments, regulatory guidance and SOP benchmarks to improve the internal PK practices.

Languages:

• Fluent Spanish
• Advanced English – Professional English proficiency

Key Competencies:

• Strong organizational skills
• Attention to detail
• Analytical mindsetEffective communication
• Stakeholder management
• Problem-solving skills
• Ability to manage multiple priorities
• Customer and service orientation
• Quality and compliance focus