Remote Clinical Coding Manager – UK

Parexel; Uxbridge; Remote; GBP 85.000 - 120.000; Vollzeit

Zusammenfassung

Parexel is seeking a Clinical Coding Manager to join the UK team in a remote capacity. You will lead coding activities, ensure adherence to guidelines, and collaborate with cross-functional teams to support clinical programs and regulatory submissions.

The role requires expert knowledge of coding dictionaries (MedDRA, WHODrug), and strong communication and analytical skills to drive quality and compliance in a regulated environment.

Qualifikationen

• Bachelor's degree in Nursing, Biology, or related field.
• 7 years of experience in a clinical coding role.
• Expert knowledge of clinical data coding methodologies and medical coding practices.
• Expert understanding of clinical research, clinical trial execution, and applicable regulatory requirements and guidelines including ICH-GCP and safety reporting requirements.
• Expert knowledge of industry-standard coding dictionaries including MedDRA and WHODrug.
• Strong communication, organization, analytical, and problem-solving skills.

Aufgaben

• Serve as the medical coding subject matter expert, driving quality and consistency across coding activities.
• Plan, direct, coordinate, and oversee clinical medical coding activities with procedures and guidelines.
• Lead coding and dictionary-related initiatives supporting clinical development and regulatory activities.
• Manage medical coding dictionaries and synonym lists, including maintenance and version updates.
• Review coded clinical data for consistency, accuracy, quality, and compliance with coding guidelines.
• Prepare and provide coding reports for medical review and decision-making.

Kenntnisse

Communication skills

Analytical thinking

Problem solving

Attention to detail

Ausbildung

Bachelor's degree in Nursing/Biology or related field

Tools

MedDRA

WHODrug

Jobbeschreibung

Parexel is seeking a Clinical Coding Manager to join the UK team in a remote capacity. You will lead coding activities, ensure adherence to guidelines, and collaborate with cross-functional teams to support clinical programs and regulatory submissions.

The role requires expert knowledge of coding dictionaries (MedDRA, WHODrug), and strong communication and analytical skills to drive quality and compliance in a regulated environment.