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