Clinical Research Associate II

📋 Description

• Monitors activities conducted by clinical investigative sites as related to AbbVie clinical studies
• Conducts site qualification, initiation, interim monitoring, and study closeout visits for Phase I
• Overviews activities of site personnel, motivates them to meet study objectives, proactively
• Ensures quality and timely submission of data, including reporting and follow-up for safety events.
• Ensures safety and protection of study subjects through compliance with monitoring plans and
• Trains study site personnel on the protocol and regulatory requirements.

🎯 Requirements

• Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred.
• Minimum of 2 years of clinically-related monitoring experience; on-site monitoring of
• In-depth knowledge of relevant therapeutic indications and regulations governing clinical research
• Familiarity with all aspects of study monitoring: data, drug accountability, documentation.
• Strong planning, organizational, analytical, and interpersonal skills; ability to communicate
• Demonstrated business ethics and integrity.

🎁 Benefits

• Innovative work culture
• Professional development
• Paid time off: vacation, holidays, personal days, and volunteer days
• Employee stock purchase
• Wellness spending account
• Flexible health insurance