Clinical Research Associate I- Principal

Mid-Sized CRO hiring Clinical Research Associates- All levels!

• Clinical Research Associate I-Principal
• 8-12 days on site per month
• Variety of therapeutic openings
• Competitive compensation package including; sign on bonus, retention bonuses, stock options, travel incentives and merit increases

Responsibilities:

• Completion of monitoring reports and follow-up letters
• Ensure good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
• Conduct all types of visits including, qualification, initiaiton, monitoring and close out
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
• Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff

Requirements:

• Minimum 1.5 years monitoring experience
• Bachelors degree in health or science related field
• Strong verbal and written communication skills