PK Data analyst

Centre for Human Drug Research; Netherlands; Hybrid; EUR 43,000 - 62,000; Full time

Benefits offered by this job

ABP pension fund

25 vacation days

Diversity Day

Holiday allowance

End-of-year bonus

Training budget

Hybrid work

Travel reimbursement

Job summary

Centre for Human Drug Research (CHDR) seeks a PK Data Analyst to join the Biometric team, analyzing PK clinical trial data and reporting findings to a diverse group of professionals.

The role requires a master’s degree in bio-pharmaceutical sciences, with programming in R as the primary language; SAS and Python familiarity are beneficial. Employment is offered as a one-year contract with hybrid work arrangements and the potential for permanent employment.

Qualifications

• Master’s degree in bio-pharmaceutical sciences.
• Strong PK knowledge; experience with PK analyses.
• Programming experience in R; SAS beneficial; Python familiarity.
• Ability to handle complex PK data and communicate results.

Responsibilities

• Develop and validate scripts for preprocessing, analyses and reporting of PK data.
• Interpret results with PK knowledge and communicate progress to stakeholders.
• Collaborate with statisticians and programmers and vendors on output delivery.
• Report PK clinical trial analyses independently.

Skills

PK knowledge

R programming

SAS knowledge

Python

WinNonLin

Data analysis

Education

Master’s degree in bio-pharmaceutical sciences

Tools

R

SAS

Python

WinNonLin

Job description

Are you passionate aboutpharmacokinetics(PK)and eager to work in an innovative environment? Join us atCentrefor Human Drug Research (CHDR)as a PK Data Analyst and become a vital part ofourBiometricsteam!You will play a key role inanalyzingPK clinical trial data, all while collaborating with a diverse group of professionals.

Pleasenote:wecanonlyconsiderapplicationsfromcandidateswhoarecurrentlyliving intheNetherlands

What does the job look like?

As a PK Data Analyst, you will be part of thePharmacokineticsteam and involved in the execution of interim and final non-compartmental analyses (NCA) of drug concentration data. Youare responsible forindependently executingthe analysis and reporting ofPK clinical trial data collected at CHDR. Yourtasksconsistof:

• Developingandvalidatingscripts required for the preprocessing,analyses, and reporting of PK data.
• Interpreting results, making it essential that you have knowledge of PK.
• Communicating aboutthe contents and progress ofyourprojectswith various stakeholders(e.g.,clients, project leaders, and statisticians).
• Collaborating with thestatistical& clinicalprogrammers and vendors on output delivery.

What CHDRoffers you

You will join a dynamic, passionate organization and work within a diverse team in a fast-paced, innovative setting.We offer you a one-year contract for a minimum of32 hours per week, with the prospect of a permanent position. The corresponding terms of employment below are based on a 40-hour workweek.

• A salary between €3.855- €5.561gross per month;
• Apensionaccrual with the ABP pension fund, with CHDR covering 70% of the pension contribution;
• 25 vacation days per year plus one Diversity Day;
• Holiday allowance andanend-of-the-year bonusranging between3.8% and 12%. Depending on company results;
• CHDR offers development opportunities with an annual budget for training;
• Our office is in a prime location: right next to Leiden Central Station, making it perfectly accessible by public transport. Your travel costs will be reimbursed up to 100%, or you can choose topurchasean (electric) bicycle at a reduced rate;?
• The possibility towork hybrid,partiallyat the office andfrom home.

Additionally,CHDRtries to stimulate a social workingenvironment by organizingdrinks,aChristmas dinner,aBBQeveningand company events such as asurvivalweekendin the Ardennes.

What you bring to CHDR?

We are looking for a Data Analyst with a solid understanding of PK. Programming and coding experience isrequired, with R being the primary language,and knowledge of SAS beneficial. Additionally, familiaritywith PythonandWinNonLinis a plus.

In this role, your ability to handle complex data and work collaboratively with others will be key to the successful completion of PK analyses.Strong analytical, problem-solvingand communication skills arerequiredfor success, just like the ability to work on multiple projects at a time by managing deadlines while keeping track of priorities.

The position requires a master’s degree inabio-pharmaceutical sciencesfield. Applicants from related fields such as bioinformatics, biomedicalengineeringor life sciences are also encouraged to apply, especially if they have a strong interest in early-phase drug discovery.

Who are we?

Since 1987, our enthusiastic and ambitious team at CHDR has been committed to conducting high-quality clinical research into the effects of both new and existing medicines. As a non-profit foundation, we take pride in contributing to scientific progress and the advancement of drug development.CHDR is located in Leiden and works in close collaboration with Leiden University and the clinical departments of the Leiden University Medical Center (LUMC).?

Centre for Human Drug Research, Zernikedreef 8, 2333 CL Leiden, the Netherlands. Tel.: [phone].