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We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world.

Proclinical is seeking a Medical Coding Lead with a focus on oncology. This role involves strategic leadership and execution of medical coding activities for clinical trials, ensuring high-quality coded data that meets industry standards and regulatory requirements. You will be part of a small global team within the Biometrics Center of Excellence, contributing to the development and implementation of coding processes.

This is a remote role based in London, the UK, or anywhere within the EU.

Responsibilities:

• Lead clinical trial coding deliverables and provide mentorship to team members.
• Develop and implement long-term coding strategies for oncology trials.
• Serve as a subject matter expert in oncology terminology and coding practices.
• Oversee coding of clinical trial data, including adverse events and concomitant medications.
• Review outsourced study-level coded data for quality and consistency.
• Maintain coding conventions and guidelines across studies.
• Manage queries related to unclear terminology or posology in data.
• Collaborate with data management and clinical development teams to optimize workflows.
• Maintain effective communication with stakeholders, including vendors and trial sites.
• Develop and manage dictionary processes, focusing on oncology-specific terms.
• Utilize medical dictionaries like MedDRA and WHODrug effectively.

Key Skills and Requirements:

• Degree in health science-related field (e.g., biology, pharmacy, nursing).
• Certification in clinical coding preferred (e.g., CCC, CPC).
• Extensive experience in medical dictionary coding, especially in oncology.
• Advanced knowledge of ICH-GCP guidelines and drug development regulations.
• Strong understanding of oncology trial design and execution.
• Expertise in medical terminology, particularly oncology-related terms.
• Experience with clinical trial data systems and EDC coding tools; Medidata Coder preferred.
• Ability to manage multiple trials and tasks efficiently in a dynamic environment.
• Excellent communication and organizational skills.
• Fluent in English, both written and spoken.
• Ability to work independently and collaboratively in a team setting.