- Full-time
To support a major manufacturer of medical devices, the full-time Senior Clinical Data Manager will oversee all aspects of clinical data management, ensuring data integrity and compliance while working remotely. Key responsibilities Support and supervise moderate to complex clinical trials, ensuring adherence to project timelines and quality standards Create and monitor data management plans, coordinating all data management activities from protocol initiation to database lock Participate in ongoing data review and oversee the correction of errors and discrepancies throughout the project lifecycle Required qualifications Bachelor's Degree in biological sciences, computer science, or a related discipline At least 4 years of clinical data management experience in Medical Devices or Pharmaceuticals Proficient in Microsoft Office and knowledgeable in GCP and regulatory requirements for clinical data management Experience with Electronic Data Capture (EDC) systems, preferably Medidata RAVE Familiarity with medical terminology and coding dictionaries such as MedDRA and WHO Drug