Clinical Research Associate
3 hours ago
About the Role
">We are seeking a skilled and experienced Clinical Research Associate to join our team. As a key member of our clinical development team, you will play a critical role in ensuring the integrity and quality of our clinical research studies.
">Key Responsibilities
">- ">
- Conduct comprehensive on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices and study protocols.">
- Develop and implement tools, procedures, and processes to ensure quality monitoring and adherence to regulatory requirements.">
- Assist in the design, implementation, and delivery of processes, programs, and policies related to clinical monitoring, ensuring alignment with organizational goals.">
- Collaborate with study teams to ensure accurate and timely data collection, entry, and reporting, addressing any discrepancies or issues promptly.">
- Provide guidance and support to lower-level professionals, including training and mentoring, to ensure consistent application of monitoring practices.">
- Manage processes and programs as needed, ensuring efficient and effective operations within the clinical monitoring function.">
- Ensure the integrity and quality of clinical data through regular audits, reviews, and verification of source documents and data entries.">
- Maintain thorough and accurate documentation of monitoring activities, findings, and corrective actions, ensuring compliance with regulatory and organizational standards.">
- Communicate effectively with study sites, investigators, and other stakeholders to address any issues or concerns related to study conduct and monitoring.">
- Stay current with industry trends, regulatory changes, and best practices in clinical research and monitoring, incorporating new knowledge into daily practices.">
Requirements
">- ">
- 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 understanding of clinical trial processes and regulations.">
- Excellent organizational and time management skills.">
- Ability to work independently and as part of a team.">
Necessary Skills
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- Proficiency in using clinical trial management systems and other relevant software.">
- Strong analytical and problem-solving skills.">
- Excellent communication and interpersonal skills.">
- Attention to detail and ability to maintain high standards of quality.">
- Ability to travel as required for on-site monitoring.">
Benefits
">This is an excellent opportunity to work with a leading biopharmaceutical solutions organization and contribute to the advancement of medical knowledge and improved patient outcomes. We offer a competitive compensation package and a collaborative work environment that values employee growth and development.
">About Us
">We are committed to creating a diverse, equitable, and inclusive culture that supports the well-being of our employees and the communities we serve. Our mission is to accelerate customer success by delivering innovative solutions and exceptional service.
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