Clinical Research Associate

Job Description

We are seeking a Clinical Research Associate with a strong commitment to advancing medical research. You will play a crucial role in the execution of clinical trials, ensuring compliance with regulatory requirements and protocols. The ideal candidate will have a solid background in clinical research and excellent organizational skills.

Responsibilities

• Oversee trial progress and report findings to the Clinical Trial Manager.
• Conduct site evaluations and feasibility assessments.
• Work closely with regulatory agencies on submissions.
• Assist in writing study protocols and ethical submissions.
• Ensure compliance with local and international regulations.
• Manage study timelines and budgets effectively.
• Act as the main point of contact for study sites.
• Foster relationships with external stakeholders.

Requirements

Education

• Bachelor's degree in Nursing or related field
• Advanced degree preferred

Experience

• 5+ years of experience in clinical research roles

Technical Skills

• Data Analysis
• Protocol Development

Soft Skills

• Attention to Detail
• Team Leadership

Certifications

• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Familiarity with clinical site management: Experience in managing relationships with clinical trial sites.
• Proficiency in medical writing: Ability to prepare regulatory documents and clinical reports.

Benefits

• Comprehensive medical aid coverage
• Retirement savings plan
• Generous leave policies
• Opportunities for career advancement

Company Culture

• Excellence: We strive for excellence in all our clinical trials and research initiatives.
• Continuous Learning: We encourage ongoing education and skills development for all employees.
• Supportive Environment: A supportive workplace where team members are encouraged to share ideas and collaborate.