Study Start Up Associate II
Posted 2 days ago
Posted 2 days ago
This is a fully remote position, open to applicants in Brazil, +1 more country.
• Oversee the commencement of clinical trials, ensuring adherence to regulatory standards.
• Assist in site initiation and activation efforts.
• Prepare and submit necessary regulatory documentation, including clinical trial applications, ethics committee submissions, and communications with regulatory agencies.
• Coordinate and engage with both internal and external stakeholders to secure approvals and authorizations for the initiation of studies.
• Manage and uphold records related to regulatory submissions, approvals, and correspondence.
• Offer guidance and support to study teams regarding regulatory requirements and best practices for study initiation.
• Take part in initiatives aimed at improving processes to enhance the efficiency of study start-up activities.
• A bachelor's degree in life sciences or a related discipline.
• At least 2 years of experience in clinical research or regulatory affairs, particularly in study start-up activities.
• Strong knowledge of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulations.
• Exceptional organizational and project management abilities, with a talent for prioritizing and managing multiple tasks concurrently.
• Outstanding communication and interpersonal skills, capable of collaborating effectively with cross-functional teams.
• Availability to travel as necessary (approximately 5%).
• Legal authorization to work in the country where the position is located.
• Competitive base salary along with performance-related incentives.
• Health and wellness programs, including medical, dental, and vision coverage where applicable.
• Retirement and pension schemes.
• Life insurance and disability coverage.
• Employee assistance programs and wellness resources.
• Opportunities for learning and development through structured training and career advancement pathways.
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