Hybrid Clinical Research Associate

Top-5 Pharma Hybrid CLINICAL RESEARCH ASSOCIATE - Accelerate Innovation & Shape the Future of Medicine.

Location: London, United Kingdom (Fully remote options available)

I'm working on an exciting opportunity with a top-5 Pharma client with a focus on a groundbreaking new treatment in Oncology, this role brings significant opportunities for growth and leadership for driven professionals.

What makes this opportunity exceptional?

• Impactful Work: Contribute to the advancement of vital medicines, impacting patient outcomes globally.
• Career Growth: Dedicated investment in your professional development, including career progression, engaged line management, technical and therapeutic area training, and peer recognition.
• Supportive Culture: Be part of our "Total Self" culture, where diversity of thoughts, backgrounds, and perspectives are celebrated, fostering a sense of belonging and taking care of our people.
• Innovation at Your Fingertips: Leverage cutting-edge tools and processes to enhance your monitoring capabilities and contribute to the evolution of clinical trial execution.

Key responsibilities:

• Own and Oversee Clinical Trial Sites: Take responsibility for managing assigned study sites, ensuring the highest standards of quality, compliance, and patient safety from initiation through close-out.
• Become a Trusted Partner: Build strong, collaborative relationships with investigators, site staff, and other stakeholders, providing guidance and support to ensure smooth and successful study conduct.
• Drive Data Integrity: Conduct thorough on-site and remote monitoring visits, performing Source Document Verification (SDV) to verify the accuracy and completeness of data and ensuring strict adherence to protocols, according to ScienceDirect.com.
• Navigate the Regulatory Landscape: Ensure meticulous compliance with Good Clinical Practice (GCP) guidelines and all applicable regulatory requirements (e.g., FDA, EMA, MHRA).
• Empower Innovation: Actively participate in the design, implementation, and improvement of monitoring tools, procedures, and processes, such as developing monitoring plans, SOPs, and training materials.

Requirements:

• Proven CRA Expertise: Minimum of 2-4 years of experience as a Clinical Research Associate, demonstrating a strong understanding of clinical trial processes and a track record of successful site monitoring.
• GCP Mastery: In-depth knowledge and practical application of ICH-GCP guidelines and relevant regulatory requirements.
• Exceptional Communication & Interpersonal Skills: Ability to build rapport, communicate effectively with diverse stakeholders, and resolve issues collaboratively.
• Autonomous & Detail-Oriented: Ability to work independently, manage multiple priorities, and maintain meticulous attention to detail in all aspects of trial oversight.
• Tech-Savvy: Proficiency in using clinical trial management systems (CTMS) and other relevant software for efficient monitoring and data handling.
• Continuous Improvement Mindset: A proactive approach to identifying opportunities for process enhancement and contributing to a culture of excellence

Tangible benefits:

• Higher band negotiable salary & Performance-Based Incentives
• Travel Allowances & Expenses: Covering per diem and travel costs for UK and EU monitoring activities.
• Private medical.
• Professional Development & Career Growth: Opportunities for training, certifications, conference attendance, and advancement to senior roles.
• Flexible Working Options
• Corporate retreats