Pharmacokinetic Scientist

Kymos Group; Cerdanyola del Vallés; Híbrido; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical manufacturing company is looking for a Pharmacokinetic Scientist to join their growing team in Cerdanyola del Vallés, Spain. This role involves acting as a principal investigator and conducting pharmacokinetic analyses to support drug development. The ideal candidate will have an MSc/PhD in relevant life sciences and strong experience with Phoenix WinNonlin software, with a commitment to GLP and GCP standards. The company offers a collaborative and empowering work environment with flexible work arrangements and a focus on continuous professional growth.

Servicios

Flexible employee benefits platform

23 vacation days per year

Fully stocked kitchen

Collaborative, empowering environment

Hybrid work model with flexible hours

Formación

• Experience with toxicology studies, bioavailability & bioequivalence testing.
• Excellent knowledge of regulatory requirements related to ADME/DMPK.
• Ability to work in a matrix environment and meet deadlines.

Responsabilidades

• Act as principal investigator and coordinator of pharmacokinetic activities.
• Design, conduct, and summarize pharmacokinetic analyses.
• Provide expert guidance into non-clinical and clinical studies.

Conocimientos

Teamwork

Personal leadership

Fluent in English

Educación

MSc/PhD in Pharmacy, Chemistry, Biochemistry, Biology, Biomedicine

Herramientas

Phoenix WinNonlin

MS Office

Descripción del empleo

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Join to apply for the Pharmacokinetic Scientist role at Kymos Group

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.
  
  
  

If you join us, you will become part of an agile and growing company with a strong scientific culture.

Here's what you can expect:

• A collaborative, empowering environment focused on continuous learning and professional growth.
• Hybrid work model with flexible Hours and intensive Fridays.
• A Flexible employee benefits platform.
• 23 vacation days per year + 24th and 31st of December as holidays.
• A Fully stocked kitchen (Coffee, fruits, snacks, and beverages).
• An inspiring workplace surrounded by nature- our headquarters located at the foot of Collserola Natural Park (Barcelona) with a Rooftop terrace an beautiful views.
  
  
  

Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic.

Requisitos:

What We Are Looking For

• MSc/PhD in Pharmacy, Chemistry, Biochemistry, Biology, Biomedicine or related Life Science
• Experience with toxicology studies, bioavailability & bioequivalence, biomarker testing, immunogenicity (ADA, Nab) testing
• Excellent knowledge of Phoenix WinNonlin software
• Knowledge of regulatory requirements and guidelines related to ADME/DMPK
• Teamwork and personal leadership
• Ability to work in a matrix environment, multi-task, meet deadlines and deal with evolving priorities
• Ability to work with MS Office package
• Fluent in oral and written English for effective communication and documentation
  
  
  

I

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research

• Industries

  Pharmaceutical Manufacturing

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