Job Summary
The Clinical Research Associate I position is located in Alameda, California, and requires an onsite work arrangement. This role is designed to maintain the highest standards of quality, accuracy, and integrity within clinical trial data throughout its entire lifecycle. The position supports a diverse team, including working mothers, female executives, and scientists.
Responsibilities
- Oversee the quality and integrity of data collected during clinical trials.
- Ensure compliance with regulatory standards throughout the trial process.
- Collaborate with research and development teams on trial execution.
- Monitor trial progress and report findings to stakeholders.
Qualifications
- A strong commitment to maintaining data accuracy and quality.
- Detail-oriented mindset for reviewing clinical research processes.
- Excellent communication and organizational skills.
- Ability to work effectively within a multidisciplinary team.
Abbott provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
