Do you want to watch clinical development change, or do you want to be the one to shape it?
Because we're hoping you're here for the latter.
Who are we?
We Are PRA Bioanalytical Labs, with locations in Lenexa, KS USA and Assen, Netherlands, EU.
We are part of the 16,000+ employees strong for PRA Health Sciences, operating in more than 90 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most.
Sample Analysis and Assay Validation
Provides key assay input to the research project and assay validation to ensure successful execution
May perform and document maintenance, trouble-shooting and repairs on advanced instrumentation with support of service engineers or other trained supervisory personnel.
Develops assays independently but with team interaction
Develops new scientific approaches to method development and communicates these to the global science team so that they can be broadly implemented.
Mentoring of more junior scientists and advising operation on developed methods.
Reviews and approves data of other scientists.
Communicates with team members and management regarding project status, purpose, scheduling, problems, etc.
Utilizes standard approach for method development
Communicates and/or participates in communication with clients regarding project status.
Maintain knowledge and skill in all techniques where you perform your work.
Provide scientific input to management and BD about new technology investments and lines of service.
Discusses scientific results with sponsors together with project manager
Promotes PRA utilizing their scientific skills through scientific communication such as external publication of posters and journal articles.
Perform R&D projects
Training of technicians on technical aspects
Quality and Timely Work Execution
Takes initiative in process development and SOP/WI writing.
Legible, logical and reproducible documentation of all experimentation.
Develops and communicates an accurate estimate of time frame for project completion.
Has a thorough understanding and complies with GLP and other appropriate regulations
Develops rugged and economical assays
Performs data review of other scientists work.
Mentor and train staff on scientific topics.
BS + 5 years of experience PhD with applicable research in a relevant Scientific field.
Presenter/Publisher in Regulated relevant Field
PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.
PRA Health Sciences