Clinical Research Associate

Job Description

Join us as a Clinical Research Associate where you will ensure the progress of clinical studies. You will work closely with clinical staff to develop protocols, monitor trial sites, and analyze data to ensure the integrity and compliance of studies.

Responsibilities

• Liaise with regulatory bodies and ethics committees.
• Assist in the preparation of regulatory submissions and audits.
• Support recruitment and retention strategies for participants.
• Evaluate and monitor site performance and quality.
• Ensure accurate data management and reporting for clinical trials.

Requirements

Education

• Bachelor's degree in Nursing or pharmacy
• Relevant research qualification is a plus

Experience

• 3+ years as a CRA or similar role

Technical Skills

• Knowledge of clinical trial regulations
• Proficient in statistical software

Soft Skills

• Problem-solving
• Interpersonal Skills

Certifications

• Good Clinical Practice (GCP) Certification
• Professional Researcher Certification

Languages

• English: Fluent

Advantageous

• Skills in patient recruitment strategies: Experience in developing effective recruitment strategies for clinical trials.
• Experience in regulatory submission preparation: Hands-on experience with preparing documents for regulatory submissions.

Benefits

• Full benefits package including health, dental, and vision.
• 401(k) matching program.
• Flexible work hours with remote work options.
• Support for continuing education and training.

Company Culture

• Commitment to Quality: Our focus is on high-quality research outcomes where ethics and adherence to guidelines are paramount.
• Employee Recognition: We celebrate achievements and contributions of our staff, recognizing hard work and dedication.
• Work-Life Balance: We promote a healthy work-life balance and offer flexible scheduling to support our employees.