Senior Clinical Data Manager 

(Utrecht, full-time, #hybrid)

 

Would you like to apply your data management expertise within an intellectual, inspiring, and international environment? Are you passionate about showing the business impact of executing clinical studies, exploring new capabilities and improving efficiency within data science?

 

As a Senior Clinical Data Manager you are responsible for setting up and maintaining data collection tools according to the Protocol, and for following the entire data management process until the database lock. You  are a member of an international multi-disciplinary study team. You are responsible for the clinical data management process in clinical trials and report to the Senior Team Leader Clinical Data Management.

 

You will perform the following tasks:

Design & validate electronic data capture instruments (eg. electronic case report) including automated data entry checks and validation of the database outputsLead and support innovation projects in the field of clinical dataAct as a mentor for junior associates in the teamWriting/ validation of the user acceptance testing (UAT) plan, Data Validation Plan (DVP) and Data Management Plan (DMP)Perform User Acceptance Testing (UAT)Perform query management and data validationSDTM mapping of clinical dataPrepare the safety review, perform medical coding and Safety Adverse Events (SAE) reconciliation in cooperation with the Medical MonitorPrepare the Data Review Meeting (DRM) and database lockMonitor timelines and risksCollaborate with and provide support to (pre)clinical and life science researchersOversight of CROs performing data management activitiesSetting up contracts with new CROs to perform data management activities

We are looking for a Senior Clinical Data Manager with the following skills and competencies:

Master's degree in Biomedical or Life SciencesMinimum of 5 years of experience in clinical data management in pharmaceutical, nutritional or academic researchKnowledge of CDISC (CDASH and SDTM)Demonstrated ability to take initiative and work independentlyHas an interest in new tools and processes, willing to learnExperience with Electronic Data Capture (EDC), MedDRA, WHO DrugProgramming experience (SAS/R/Python)Fluent in English (speaking and writing)A solid understanding of biomedical research, clinical trials, and Good Clinical Practice (GCP), drug/product developmentPragmatic attitude and being adaptable to the changing needs of the business, being agile and flexible 

Working here you’ll need to enjoy a fast-pace, complexity and it can get a little challenging. But it’s packed with opportunities. You’ll work with some of the best-known brands in the world, such as Evian, Nutricia, Activia and Nutrilon and we absolutely guarantee that you can just be yourself. Be innovative and entrepreneurial and the impact you could make might just amaze you. Join our movement for a healthier world. One Planet One Health BY YOU.

 

We are proud to be an equal employer. We are convinced our differences make the difference and that an inclusive working environment will drive our growth as a business, as teams and as individuals. We will therefore consider all applicants for employment* fostering an inclusive working culture that is accessible for all.

 

Did you know that as a B-Corp certified company, Danone Benelux meets the highest verified standards of social and environmental performance, transparency, and accountability?

 

We Offer

At Danone, we offer a complete package of benefits, with a competitive primary salary and yearly bonus, but also benefits like a premium free pension, 30 days annual leave and several discounts on a collective health insurance and even on some of our products. In the Netherlands we also offer a hybrid working environment which enables each team to meet our people's desire for flexibility. Across our 3 office hubs in Hoofddorp, Zoetermeer and Utrecht this helps us create better opportunities for connection & synergies across our entities, teams, functions and categories.

What’s next?

Hit the “apply now” button. After your application deadline first feedback will follow within 2 weeks. In case you are invited to the selection process you should expect to receive feedback 2 weeks after each step of the process

To comply with GDPR regulations, we cannot process your personal data without given consent. Therefore, we strongly recommend applying directly via our website.

 

Need more information? Please contact Valerija Usova, Talent Manager via valerija.usova@danone.com.

 

* all applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

#LI-NL