Please review the list of current career opportunities below. We also encourage you to check back regularly for newly posted opportunities. If you are interested in one of the available positions and feel that you meet the required qualifications, please email your resume to .
If your resume meets our needs, we will contact you by phone within 7-10 business days. Due to the high volume of resumes that we regularly receive, we will be unable to notify you if your resume does not meet our needs at this time.
We are currently looking for home based (regional US) Clinical Research Associates (CRAs) to monitor and manage clinical investigative sites to ensure adherence to procedures, protocols, and project plans. All therapeutic areas considered. Senior levels considered on experience and therapeutic expertise.
Additional unique growth opportunities toward field and regional management within a robust decentralized model with bold leadership.
Required Experience
Qualified candidates will have two years of monitoring experience with a bachelor?s degree in life sciences, nursing or other health-related discipline. Strong working knowledge of Federal Code of Regulations and GCP guidelines are required.
Education Requirements
Successful candidates will also have bachelor?s degree in life sciences, nursing or other health-related discipline.
www.paragonbiomedical.com
Reports to the Director of Global Biostatistics & SAS programming. Supports Paragon Data Operations department by providing expert statistical input into and review of statistical deliverables to meet the requirements of internal and external clients. Coordinate and/or develop Statistical Analysis Plans (SAP), mock-up tables, programming and derived dataset specifications. Protocol development including experimental design, randomization, sample size calculation, statistical methods, defining study objectives and parameters. Write the statistical section of the Clinical Study Report (CSR) and collaborate with medical writer in preparing the integrated CSR. Perform QC of TFL and derived datasets. Programming of derived datasets and Tables, Figures and Listings (TFL), perform data review and statistical analysis. Collaborate with Data Management by reviewing DMPs, CRFs and edit check specifications. PhD or Master’s in statistics. Other duties commensurate with the position as assigned by line manager. PhD + 2 year or MS + 5 years experience in pharmaceutical and/or CRO environment Direct CRO experience preferred. Software is Microsoft Office with several custom windows based applications and programming software. Statistical Programming using the SAS system. 10 – 20% travel.