Job Description

Join our dynamic team as a Clinical Research Associate and play a vital role in advancing healthcare by ensuring the successful implementation, monitoring, and completion of clinical trials. Your efforts will contribute to the safety and well-being of patients while adhering to the highest standards in clinical research.

Why You Should Apply

• Make a Difference : Be a part of groundbreaking research that can improve patient lives.
• Professional Growth : Work in a stimulating environment with opportunities to expand your skill set.
• Collaborative Environment : Develop strong relationships with clinical investigative sites and a supportive team.
• Flexibility : Enjoy a balance between remote work and occasional office presence.

What You’ll Be Doing

• Acting as the primary liaison for assigned study sites, ensuring compliance and resolving issues.
• Attending Investigator Meetings and study-specific training.
• Conducting pre-study qualification visits, site initiation, routine monitoring, and close-out visits.
• Developing and maintaining collaborative relationships with clinical sites.
• Monitoring recruitment, data quality, and ensuring regulatory compliance.
• Collaborating with data management to meet data cut and lock deadlines.
• Assisting in preparation for audits/inspections.

About You

• A minimum of 4-10 years of on-site and remote monitoring experience is required.
• Bachelor's degree, preferably in life sciences.
• Experience with remote or risk-based monitoring is preferred.
• Proficiency in GCP and understanding of clinical trial management.
• Strong communication and interpersonal skills.
• Comfortable working in an entrepreneurial, small company environment.
• Self-starter with the ability to interact with global teams.

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