Clinical Statistician

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Job description

*Are you the perfect candidate**?*

For a CRO we are looking for an experienced, communicative and proactive (Clinical) Statistician.
Can you provide expertise in the creation of research protocols and associated SAPs with an emphasis on prospective clinical trial design, power and sample size calculation, and hypothesis testing along with associated statistical methods?
And can you provide expertise in the creation, quality control and maintenance of clinical programming for the statistical outputs?
Do you want to support the review and/or development of study protocols, recognizing and highlighting statistical issues in collaboration with internal and external colleagues with minimal supervision?
Then you are our perfect candidate!

*Do you have:*

* A PhD (with at least 5 years of experience supporting clinical trials) or a Master's degree (with minimum of 8 years of experience) in Statistics (preferred), Epidemiology, or Mathematics
* A strong background in trial design and statistical models ideally in a drug development setting (e.g. pharmaceutical industry, biomedical research)
* Experience in in supporting protocols, writing SAPs, and in the production of TLFs for clinical trials using SAS
* Strong understanding of how observational data sources can be used for statistical inference
* Strong communications skills to explain and resolve statistical analysis issues, ability to communicate (verbal and written) technical and non-technical information clearly to a diverse audience

*Y**our tasks and responsibilities: *

* Creating or advising on study protocols or analysis plans across multiple therapeutic areas in collaboration with internal and external functional experts
* Executing or overseeing the execution of study plans or protocols using either SAS or R which address data preparation, derivation of study variables (including CDISC as applicable), and performing statistical modelling and/or testing
* Provide Quality Control for (statistical) analysis programs and deliverables
* Follows internal and external procedures, best practice guidelines (e.g. ICH-GCP E9), and regulations. Provides project guidance on issues pertaining to regulations and guidelines
* Collaborating with the project team to design the CRFs (in conjunction with a Data Manager), methodologies, and (statistical) techniques to address complex study objectives
* Contributing to the development of innovative methodologies and new offerings.

*The client offers*

* An open culture in an innovative and dynamic environment with inspiring colleagues and good working conditions
* An environment where you have room to be creative, take initiative and have direct influence on the way we work
* After COVID we intend to offer the option of working from home, working at the office or a combination of the two

*Are you ready to become part of their story?*

*Our recruitment process*
We go beyond traditional recruitment; we work closely with you to ensure an unrivaled, personal candidate experience throughout our entire process.

Our relationship with this client allows us to fully support you through the recruitment process, providing you with all the role insight and knowledge you need for this 2 part interview process.

Our recruitment process is entirely confidential. Your details will never be shared without your prior consent.
If you would like to be considered for this position, please send in your English CV in WORD format to