Clinical Research Associate Senior
2 weken geleden
We are seeking a highly skilled and experienced Sr. Clinical Research Associate to join our team at Allucent. As a Sr. CRA, you will play a critical role in ensuring the successful execution of clinical trials, working closely with our clients and site staff to deliver high-quality results.
Key Responsibilities:- Monitor and manage clinical trial sites to ensure compliance with Good Clinical Practice (GCP) and applicable regulations.
- Conduct site visits, audits, and inspections to assess site performance and identify areas for improvement.
- Develop and implement corrective actions to address site issues and ensure compliance with trial protocols.
- Collaborate with project teams to develop and implement trial strategies, including monitoring plans and site management plans.
- Provide training and support to site staff on trial protocols, GCP, and regulatory requirements.
- Ensure timely and accurate reporting of trial data and progress to clients and regulatory authorities.
- At least 5 years of experience in clinical research, with a strong background in GCP and regulatory compliance.
- Relevant life science degree or medical background, or combination of education and experience.
- Excellent communication and interpersonal skills, with the ability to work effectively with clients, site staff, and project teams.
- Strong analytical and problem-solving skills, with the ability to identify and resolve complex issues.
- Proficiency in computer applications, including Microsoft Office and clinical trial management systems.
- Competitive salary and benefits package.
- Opportunities for professional growth and development, including training and mentorship.
- Collaborative and dynamic work environment.
- Flexible working hours and remote work options.
We are an equal opportunities employer and welcome applications from diverse candidates. If you are a motivated and experienced Sr. CRA looking for a new challenge, please submit your application.
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