*work schedule*
standard (mon-fri)
*environmental conditions*
office
*job description*
join us as a clinical data assoc ii – make an impact at the forefront of innovation
we have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a clinical data assoc ii, you will perform advanced aspects of the data cleaning process with a high level of accuracy and in accordance with good clinical practices (gcps) and standard operating procedures/work process documents (sops/wpds), to assess the safety and efficacy of investigational products and/or medical devices.
What you’ll do
identify, resolve, and update data discrepancies. Make changes to the data management database as required. Generate, track and resolve data clarifications and queries. May implement crf design in identified graphic design package. Review data listings for accuracy and consistency of data. Analyze and resolve data validation and other data management reports. Produce project-specific status reports for cdm management and for clients on a regular basis. Perform data management activities such as serious adverse event and third party vendor reconciliations as well as data listing reviews.
Education and experience requirements
high / secondary school diploma or equivalent and relevant formal academic / vocational qualification technical positions may require a certificate previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 6 years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient fo