Description
Key features --Creating technical blueprints and technical documentation.
-Providing analytical problem solving skills.
-Providing feedback and insight on technical design discussions.
-Creation of monitoring reports.
-Ensuring the timely delivery of data into all clinical trial databases.
Skills an Experience -
-Bachelor's degree in a clinical, scientific, or related field, or equivalent work experience required.
-Ideal candidate will have at least 1 year of relevant experience in a biopharmaceutical company, CRO or academic setting.
-Experience with one or more EDC systems helpful
-Experience with database software, Microsoft Word, Excel, Powerpoint
-Excellent communication and interpersonal skills to effectively interface with others in a team setting.
-Excellent organizational skills, attention to detail, and a customer service demeanour.
-Experience in SAS Programming is a plus.
This is an exciting opportunity to work for an emerging leader in the pharmaceutical industry. Please submit your updated resume in order to be considered for this opportunity.
To find out more about Real please visit www.realstaffing.com