I have completed a Masters program in Biotechnology. I have keen interest in Clinical Research and Regulatory Affairs. I am looking for an entry level Clinical or Regulatory position. I have research site coordination experience in the areas of Rheumatology and Pain research. I am also ICH and GCP certified.

Highlights:

• CRF writing
• patient follow up
• administering informed consent form
• administering psycometric scales
• source documents review
• Reporting SAE’s
• Pre-screening and recruiting patients
• -Submitted documents to the Ethics Committee
• Rheumatology
• Pain