Project Leader Dmpk To Astrazeneca Gothenburg

Alten Sverige AB / Biomedicinjobb / Göteborg
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About AstraZeneca
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a phenomenal workplace culture that encourages innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

We are looking for a motivated individual to take on take on the role as Drug Metabolism and Pharmacokinetics (DMPK) Project Leader (DPL) for 12 months. Alternatively, it can be an opportunity for a highly talented indivudal with less specific experience to assist an experienced DPL whilst training for the role. The DPL role is a strategic and scientific role where you will be a member of the project team and work cross functionally and closely with the toxicologist, bioscientist and clinical pharmacologist in various stages of drug development beginning with candidate drug nomination. You will lead and coordinate all non-clinical DMPK work including assessment of drug-drug interaction potential, pharmacokinetic/pharmacodynamic data analysis, estimation of safety margins, biotransformation (including human) and delivery of non-clinical pharmacokinetics regulatory summary documents for compound progression.

You are expected to have understanding of DMPK and drug development to be able to provide advice and interpretation of complex data.

Main Duties and Responsibilities:
• Lead DMPK- activities related to evaluating, mitigating and highlighting any development risks related to pharmacokinetic and pharmacodynamic drug properties including absorption, distribution, clearance, elimination and biotransformation.
• Deliver DMPK data and interpretation to projects within agreed timelines and to the right quality
• Accountable together with Bioscience and Toxicology functional leads to plan and conduct non-clinical studies of drug candidtes to support first in human dosing.
• Apply an understanding of DMPK and regulatory requirements to address DMPK related risks and take advantage opportunites for simplification.
• Responsible for leading, coordinating and engaging with Early RIA DMPK colleagues and contract research organizations in project related activities.
• Prepare clear presentations related to the above for internal governance bodies.

Requirements:
• Formal training or proven experience of working with pharmacokinetics and drug metabolism.
• Hands-on knowledge of pharmacokinetic data analysis.
• PhD or equivalent experience in a relevant discipline (Pharmacokinetics, toxicology, , Pharmaceutics).
• Understanding of regulatory requirements related to DMPK and ADME
• Experience from drug discovery or development cross-functional project work is desirable
• Ability to engage and collaborate across boundaries with a problem solving attitude and focus on delivery

What we offer you at ALTEN
Every employee is equally valuable in the success of ALTEN! We are driven by making people grow and develop, which is why we offer you the opportunity to work with what you are truly passionate about. At ALTEN, we have a broad range of assignments at most of the leading companies in Sweden in several different sectors, to make it possible for your wishes to come true. We offer both national and international opportunities and together with your coaching manager, you build your career path so you constantly are able to develop and achieve your goals and dreams!

As a consultant at ALTEN, you will get the genuine team feeling at your assignment but also a wonderful togetherness at ALTEN. Through our different internal networks, such as ALTEN Sports, Women@ALTEN and ALTEN Innovation you will get the opportunity to drive topics and activities that are close to your heart, together with your colleagues. All activities are of course optional. Work life balance is our top priority. We also have a collective agreement and other benefits like Pension, Insurances and Wellness grants.

We believe in growing together!

Please note: Between 20th December and 8th January we will not be able to answer questions and no selection will be made during this period. Merry christmas and Happy new year!

Varaktighet, arbetstid
Heltid Tillsvidareanställning

Publiceringsdatum
2019-12-20

Ersättning
Enligt överenskommelse

Så ansöker du
Sista dag att ansöka är 2020-01-15
Klicka på denna länk för att göra din ansökan

Företag
Alten Sverige AB

Omfattning
Detta är ett heltidsjobb.

Arbetsgivare
Alten Sverige AB (org.nr 556420-7453)

Jobbnummer
5013606

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