Job Summary
The Clinical Research Associate at Integrated Resources, Inc. is part of a highly experienced team committed to advancing the clinical research field. This role focuses on supporting the planning and execution of clinical trials by engaging in various operational activities, ensuring that all processes comply with industry standards and regulatory requirements.
Responsibilities
- Assist in the arrangement and management of investigator meetings.
- Provide on-site support during clinical trials when required.
- Collaborate with team members to ensure trial operations align with study protocols.
- Monitor compliance with regulatory and ethical standards during clinical operations.
Qualifications
- Experience in clinical research and a solid understanding of the relevant regulations.
- Ability to work collaboratively with a diverse team of professionals.
- Strong organizational skills and attention to detail.
- Excellent communication abilities, both written and verbal.
Integrated Resources 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.
