Senior Clinical Study Manager

📋 Description

• Lead assigned clinical research activities
• Partner with internal stakeholders, investigators, and KOLs to develop and review study design and
• Plan and execute clinical studies including site selection, patient recruitment, study documents
• Conduct clinical studies on schedule and within budget while ensuring high quality and compliance
• Perform on-site and remote site qualification, initiation, monitoring, and close-out visits
• Conduct clinical study monitoring to ensure regulatory and protocol compliance and data accuracy

🎯 Requirements

• Advanced degree in scientific/bioengineering field (M.S., Ph.D., or M.D.) with 5+ years clinical
• Experience managing medical device trials
• Knowledge of clinical and/or outcomes research study design
• Proven experience in protocol and ICF development and writing clinical sections for regulatory
• Proven experience in conducting literature searches, reviews, and appraisal of scientific data
• Excellent ability to interact with physicians and professionals

🎁 Benefits

• Market-competitive compensation packages including base pay, incentives, benefits, and equity
• Remote work opportunity