Serve in support-level capacity on a Clinical Data Management team to provide efficient, quality data management products that meet customer needs. Responsible for study management and execution of studies as per the established Standard Operating Procedures (SOP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP) best practices and regulatory requirements
If interested, send you resume and contact details.
I have briefly read the description on clinical research , and I can deliver as per the requirements however I need us to discuss for more clarity on the details........
Hi there, I am a Microbiologist by profession. I am sure I am the right candidate for this project. I am very hardworking and honest person. I assure you quality work. looking forwards