Drug Safety Coordinator: Pharmacovigilance & Data Ops

Viking Therapeutics, Inc.; San Diego (CA); On-site; USD 77,000 - 90,000; Full time

Job summary

Viking Therapeutics, Inc. is seeking a Drug Safety Associate in San Diego, CA to provide crucial operational and documentation support in clinical safety and pharmacovigilance. The role involves ensuring timely safety oversight across multiple studies and maintaining safety logs and documentation.

The ideal candidate will have a BA degree in a relevant field and 1-3 years of experience in drug safety or clinical research. A strong attention to detail and proficiency in Microsoft Office are essential for this position.

Qualifications

• Minimum of 1–3 years of relevant experience in drug safety or clinical research.
• Familiarity with clinical trial operations and safety reporting concepts.
• Strong attention to detail and ability to manage multiple tasks simultaneously.

Responsibilities

• Track safety case flow and status across clinical studies.
• Review and quality check safety data outputs.
• Coordinate collection and filing of safety documents.
• Assist with preparation for audits and inspections.

Skills

Clinical research experience

Drug safety/pharmacovigilance knowledge

Microsoft Office Suite proficiency

Effective communication skills

Education

BA degree in Nursing, Pharmacy, or related discipline

Clinical credential or healthcare certification preferred

Job description

Viking Therapeutics, Inc. is seeking a Drug Safety Associate in San Diego, CA to provide crucial operational and documentation support in clinical safety and pharmacovigilance. The role involves ensuring timely safety oversight across multiple studies and maintaining safety logs and documentation.

The ideal candidate will have a BA degree in a relevant field and 1-3 years of experience in drug safety or clinical research. A strong attention to detail and proficiency in Microsoft Office are essential for this position.