Clinical Research Associate
il y a 2 semaines
As a leading global contract research organization (CRO), Fortrea is seeking a highly motivated and experienced professional to join our team as a Clinical Research Associate. In this role, you will be responsible for managing clinical trials and ensuring compliance with regulatory guidelines.
Key Responsibilities:- Manage clinical trials from start to finish, ensuring timely and efficient execution
- Develop and maintain strong relationships with site staff, investigators, and other stakeholders
- Ensure compliance with regulatory guidelines, including ICH-GCP and local regulations
- Collaborate with cross-functional teams to identify and mitigate risks
- Provide training and support to site staff on clinical trial procedures and protocols
- Fluent in local languages and business proficient in English (verbal and written)
- Good understanding of global, country/region clinical research guidelines
- Hands-on knowledge of Good Documentation Practices
- Good IT skills, including MS Office and clinical IT applications
- Strong MS Excel skills
Fortrea is a global CRO with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
We are committed to diversity and inclusion in the workforce and do not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual.
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