Pharmacovigilance database management (MedWatch, Eudravigilance, or similar systems)

Electronic Case Tracking Systems (eCTS) and Clinical Trial Management Systems (CTMS)

Microsoft Office Suite (Word, Excel, PowerPoint, Access)

Medical coding and terminology (MedDRA preferred)

Data analysis and reporting tools

Regulatory document preparation and submission

Safety database maintenance and query management

Signal detection methodologies and statistical analysis

Attention to detail and accuracy in documentation

Strong analytical and problem-solving abilities

Excellent communication and interpersonal skills

Ability to work collaboratively in cross-functional teams

Time management and organizational skills

Regulatory compliance mindset and ethical standards

Adaptability to changing regulatory requirements

Professional judgment and decision-making capability

Proactive approach to identifying and resolving safety issues