Job Summary
The Clinical Research Associate 2 (CRA2) at Emerald Clinical Trials plays a vital role in advancing clinical research by collaborating with over 160 biotech firms. This position is essential for the identification, feasibility evaluation, and selection of investigators and sites involved in clinical trials, ensuring that all components are effectively managed.
Responsibilities
- Support the identification and assessment of potential investigators and trial sites.
- Conduct feasibility studies to determine site capabilities for clinical trials.
- Ensure compliance with regulatory requirements and company standards.
- Collaborate with the clinical study team to achieve trial objectives.
- Complete relevant documentation and reporting activities promptly.
Qualifications
- Experience in clinical research, preferably in a CRA role.
- Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work effectively in a fast-paced, onsite environment.
- Proficiency in using clinical trial management systems and relevant software.
Emerald Clinical Trials 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.
