Clinical Research Associate

Job Description

As a Clinical Research Associate, you'll take ownership of clinical monitoring, data integrity, and site management. Your role is vital in ensuring that trials run smoothly and yield reliable results that contribute to meaningful health advancements.

Responsibilities

• Coordinate and monitor clinical trials to ensure regulatory compliance and adherence to study protocols.
• Serve as the main point of contact between the study site and the organization.
• Collect, review, and manage study data, ensuring accuracy and completeness.
• Ensure informed consent is obtained and documented appropriately.
• Conduct site visits to assess adherence to protocols and timely enrollment of participants.
• Support the training and onboarding of site staff and investigators on study protocols.

Requirements

Education

• Bachelor's degree in Life Sciences or related field
• Master's degree is a plus

Experience

• 2+ years of experience in clinical research roles

Technical Skills

• Good Clinical Practice (GCP)
• Data Analysis

Soft Skills

• Attention to Detail
• Communication Skills

Certifications

• Certified Clinical Research Associate (CCRA)
• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Experience with Electronic Data Capture (EDC) systems: Familiarity with EDC platforms for efficient data management.
• Knowledge of regulatory submission processes: Understanding of how to prepare and submit protocols for regulatory approval.

Benefits

• Competitive salary package
• Medical aid and health benefits
• Flexible working hours
• Professional development opportunities

Company Culture

• Collaboration and Teamwork: We promote a culture of teamwork and collaboration to achieve common goals.
• Passion for Research: Our team is dedicated to conducting impactful research that transforms patient care.
• Commitment to Ethics: We value ethical practices and integrity in conducting all aspects of our research.