Senior Clinical Research Associate

Shape the Future of Clinical Research with Fortrea

As a Senior Clinical Research Associate, you will play a pivotal role in ensuring the success of clinical trials by managing and monitoring study sites. You'll work closely with investigators and sponsors to uphold regulatory standards and deliver high-quality data that advances medical breakthroughs.

Key Responsibilities

• Monitor and manage clinical study sites, including initiation, routine visits, and closeout activities.
• Ensure patient safety and compliance with informed consent and protocol requirements.
• Review source documents and verify data integrity on Case Report Forms (CRFs).
• Prepare accurate and timely monitoring reports and maintain study files.
• Serve as lead monitor for assigned protocols and assist in developing monitoring plans.
• Coordinate with vendors and internal teams to meet project timelines and objectives.
• Support feasibility assessments, budget negotiations, and regulatory submissions.
• Mentor and train junior team members through co-monitoring and guidance.
• Travel extensively (60–80%) to support site activities and maintain audit readiness.

Qualifications

• Bachelor's degree in life sciences or related field, or equivalent clinical research experience.
• Typically a minimum 3 years of clinical monitoring experience in pharmaceutical or CRO settings.
• Strong knowledge of regulatory requirements and drug development processes.
• Advanced site monitoring and management skills.
• Excellent communication, organisational, and problem-solving abilities.
• Proficiency in relevant computer applications and systems.
• Valid driver's license and ability to travel extensively.

Why Join Fortrea

• Contribute to groundbreaking research that improves lives worldwide.
• Access robust training, mentorship, and advancement opportunities.
• Thrive in a collaborative, inclusive environment that values work-life balance.
• Be part of a forward-thinking organisation shaping the future of clinical trials.