Clinical Research Associate
4 weeks ago
About the Role
We are seeking a highly skilled Clinical Research Associate to join our team in the pharmaceutical industry. As a Clinical Research Associate, you will be responsible for monitoring and quality assurance of clinical trials, with a focus on oncology trials.
Key Responsibilities:
- Monitor and manage clinical trials, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements.
- Conduct site visits to ensure trial integrity and quality.
- Develop and maintain strong relationships with investigators, site staff, and other stakeholders.
- Provide training and support to site staff on trial procedures and protocols.
- Collaborate with cross-functional teams to ensure trial success.
Requirements:
- Bachelor's degree in a life science or related field.
- Minimum 2 years of experience in clinical research, preferably in the pharmaceutical industry.
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to travel up to 50%.
What We Offer:
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- Collaborative and dynamic work environment.
- Recognition and rewards for outstanding performance.
How to Apply:
Please submit your application through our website, including your resume and a cover letter outlining your experience and qualifications.
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