
Senior Clinical Research Specialist
2 weeks ago
Synergize with our agile team to accelerate the delivery of therapies.
About This RoleWe are seeking a skilled Clinical Research Associate to join our organization. The successful candidate will conduct comprehensive on-site and remote monitoring of clinical research studies, ensuring compliance with widely accepted clinical practices and study protocols.
The ideal candidate will have a strong understanding of clinical trial processes and regulations, as well as excellent organizational and time management skills. They will be able to work independently and as part of a team, communicating effectively with study sites, investigators, and other stakeholders.
Key Responsibilities- Develop and implement tools, procedures, and processes to ensure quality monitoring and adherence to regulatory requirements
- Collaborate with study teams to ensure accurate and timely data collection, entry, and reporting
- Provide guidance and support to lower-level professionals, including training and mentoring
- Maintain thorough and accurate documentation of monitoring activities, findings, and corrective actions
- Stay current with industry trends, regulatory changes, and best practices in clinical research and monitoring
- Bachelor's degree in a relevant field such as life sciences, nursing, or a related discipline
- Previous experience in clinical research or a related field is preferred
- Strong analytical and problem-solving skills
- Excellent communication and interpersonal skills
- Ability to travel as required for on-site monitoring
- Proficiency in using clinical trial management systems and other relevant software
- Attention to detail and ability to maintain high standards of quality
- Ability to adapt to changing priorities and deadlines
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