Clinical Research Associate
vor 1 Monat
We are seeking a highly skilled and experienced Clinical Research Associate to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for ensuring the smooth execution of clinical trials, from site initiation to close-out.
Key Responsibilities- Monitor and manage clinical trial sites to ensure compliance with Good Clinical Practice (GCP), International Conference on Harmonisation (ICH) guidelines, and study protocols.
- Conduct site initiation, monitoring, and close-out visits to assess site performance and identify potential issues.
- Collaborate with cross-functional teams, including project management, clinical operations, and regulatory affairs, to ensure seamless trial execution.
- Develop and maintain strong relationships with site staff, investigators, and other stakeholders to ensure effective communication and issue resolution.
- Identify and mitigate potential risks and issues, and develop contingency plans to ensure trial continuity.
- Ensure accurate and timely data collection, reporting, and documentation, and maintain a high level of data quality.
- Participate in the development and implementation of study protocols, informed consent forms, and other study-related documents.
- Contribute to the development and maintenance of clinical trial documentation, including trial master files and investigator site files.
- At least 5 years of clinical monitoring experience, with a strong background in GCP, ICH, and clinical trial regulations.
- Relevant life science degree or healthcare background, with a strong understanding of medical terminology and clinical trial processes.
- Excellent communication, interpersonal, and organizational skills, with the ability to work effectively in a fast-paced environment.
- Strong analytical and problem-solving skills, with the ability to identify and mitigate potential risks and issues.
- Proficiency in computer applications, including Microsoft Office and clinical trial management systems.
- A comprehensive benefits package, including health insurance, retirement plan, and paid time off.
- A competitive salary and bonus structure, with opportunities for career growth and professional development.
- A dynamic and supportive work environment, with a focus on teamwork and collaboration.
- Opportunities to work on a variety of clinical trials, with a focus on innovative and cutting-edge research.
- A commitment to diversity, equity, and inclusion, with a focus on creating a welcoming and inclusive work environment.
We are an equal opportunities employer and welcome applications from diverse candidates. If you are a motivated and experienced clinical research professional looking for a new challenge, please submit your application, including your resume and cover letter, to [insert contact information].
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