Clinical Research Associate
4 weeks ago
We are seeking a highly skilled Clinical Research Associate to join our team in the Oncology Trials department. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials, ensuring compliance with regulatory requirements and Good Clinical Practice guidelines.
Key Responsibilities- Monitor and manage clinical trials, including site initiation, data collection, and study close-out
- Ensure compliance with regulatory requirements and Good Clinical Practice guidelines
- Collaborate with cross-functional teams, including study managers, data managers, and biostatisticians
- Develop and maintain site start-up documents, including SIV agendas
- Provide training and support to site staff on study protocols and procedures
- Conduct site visits and provide feedback to site staff on study performance
- Assist with the development and implementation of patient recruitment strategies
- Collaborate with investigators and site staff to ensure timely completion of studies
- Bachelor's degree in a life science or related field
- Minimum 2-3 years of experience in clinical research, preferably in the pharmaceutical industry
- Experience in Oncology trials is highly desirable
- Strong analytical and problem-solving skills
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
- Proficiency in Microsoft Office and clinical trial management systems
- Competitive salary and benefits package
- Opportunities for professional growth and development
- Collaborative and dynamic work environment
- Recognition and rewards for outstanding performance
We are an equal opportunities employer and welcome applications from diverse candidates. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.
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