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Clinical Research Associate
3 weeks ago
We are seeking a Clinical Research Associate to conduct on-site and remote monitoring of clinical research studies, ensuring compliance with widely accepted clinical practices. This role involves reviewing study protocols, informed consent forms, and case report forms.
The ideal candidate will have strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements. They will also possess excellent communication and interpersonal skills, with the ability to work independently and manage multiple priorities.
Key Responsibilities- Conduct on-site and remote monitoring to ensure adherence to clinical practices.
- Develop and implement tools, procedures, and processes to ensure quality monitoring.
- Collaborate with cross-functional teams to support clinical trial operations.
- Bachelor's degree in a related field or equivalent experience.
- Minimum of 2–4 years of experience in clinical research monitoring.
- CCRA certification or equivalent preferred.
- CCRA certification or equivalent preferred.
- Attention to detail, strong analytical and problem-solving skills.
- Excellent time management and organizational skills.
This role offers opportunities for career development, progression, training, peer recognition, and total rewards programs. We strive to build a workplace where diverse thoughts, backgrounds, cultures, and perspectives are valued and everyone belongs.
Why Join UsWe are dedicated to building a diverse, inclusive, and authentic workplace. If your past experience doesn't align perfectly, we encourage you to apply anyway. We invite you to join our Talent Network to stay connected to opportunities.
