Description
Key Features:-Excellent analytical, problem-solving, organizational, time-management, interpersonal and communication skills
-Knowledge of all aspects of the clinical trials process from pre-clinical to post-marketing phases
-Ability to interpret and apply regulatory requirements
-Knowledgeable concerning all aspects of qualification and compliance assessments
-Demonstrated ability to effectively partner with ESPs
-Technical understanding of clinical research technologies and software development methodologies
-Experience in systems integration and the application of data interchange standards
-Proficient in the use of one or more of the leading Clinical Database Management Systems or clinical programming environments
-Experience supporting continuous process improvement initiatives
-Current with industry developments, trends and opportunities
Education and/or Experience: Minimum: BA/BS + 2 years experience or equivalent
Preferred: 2+ years of clinical systems or programming experience in the Pharmaceutical, Device or Biotech industries (Sponsor, CRO or combination) in roles of increasing responsibility.
This is an excellent opportunity to become a part of a well established organization within the pharmaceutical and medical device industry. Please submit your current resume in order to be considered for an interview.
To find out more about Real please visit www.realstaffing.com