Clinical Research Associate II
vor 4 Wochen
About the Role
We are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a Clinical Research Associate II, you will play a critical role in the success of our clinical trials by ensuring that all study activities are conducted in accordance with Good Clinical Practice (GCP), International Conference on Harmonisation (ICH) guidelines, and applicable regulations.
Key Responsibilities
- Conduct site initiation, monitoring, and closure visits to ensure compliance with study protocols and regulations.
- Monitor and track study data to ensure accuracy and completeness.
- Prepare and review regulatory documents, including informed consent forms and study protocols.
- Collaborate with the project team to identify and mitigate potential issues.
- Develop and maintain strong relationships with site staff and investigators.
- Ensure the continuous maintenance of the Trial Master File and Investigator Site File.
- Participate in the start-up process, including preparing study documents and site contracts.
- Assist the project team with the day-to-day management of critical studies.
Requirements
To be successful in this role, you will possess:
- At least three years of clinical monitoring experience and/or relevant clinical trial experience.
- A relevant life science degree or healthcare background.
- Sound knowledge of medical terminology and clinical monitoring processes.
- Strong communication and interpersonal skills.
- Ability to work independently and prioritize tasks effectively.
- Proficiency with various computer applications, including Word, Excel, and PowerPoint.
Benefits
As a Clinical Research Associate II at Allucent, you will enjoy a comprehensive benefits package, competitive salary, and opportunities for professional development and growth. You will also have the chance to work in a dynamic and fast-paced environment with a team of dedicated professionals who are passionate about making a difference in the lives of patients.
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