Pharmacovigilance Specialist - US - Remote

Worldwide Clinical Trials is hiring a Pharmacovigilance Specialist for a remote, full-time role. The job is open to candidates in the United States, and the posted salary range is USD 50,000 to 99,000 per year. You would collect, process, evaluate and report incoming Serious Adverse Event (SAE) data under regulatory guidelines, the company's Standard Operating Procedures and project-specific instructions.

The position is listed as an Associate, Pharmacovigilance role. You would serve as Lead PV Associate on small to moderate sized studies that are simple to moderate in complexity and scope, with support from senior staff.

What you will do

• Author the Safety Management Plan for assigned studies
• Review incoming SAE data for completeness and accuracy
• Perform data entry in the Safety Database and complete applicable tracking of incoming safety information
• Generate queries for missing or unclear information and follow up with sites for resolution
• Perform quality control of SAEs processed by other PV Associates
• Generate regulatory reports and perform safety submissions as needed

What they are looking for

• Good understanding of medical and scientific terminology, the principles of clinical assessment of adverse drug events, international regulations and reporting requirements
• Good understanding of computer technology and management of relational database systems, including extraction of data
• A positive attitude and the ability to interact diplomatically and professionally with internal and external customers in a global environment
• Excellent organization skills and the ability to handle multiple competing priorities within tight timelines
• Consistent commitment, dependability, cooperation, adaptability and flexibility in daily tasks and responsibilities
• Ability to anticipate needs and follow through on all assigned tasks

Your experience

• Bachelor's degree in a science-related field, nursing, or equivalent
• Minimum of 1 year of pharmacovigilance experience in pre-approval clinical trials
• Equivalent combination of relevant education and experience
• Computer literacy and strong working knowledge of MS Office applications (Excel, PowerPoint, Word)
• Excellent written and verbal communication skills
• Excellent organization skills and attention to detail
• Demonstrated ability to handle multiple competing priorities while adhering to applicable timelines
• Ability to work independently, prioritize work effectively and work successfully in a matrix team environment
• Ability and willingness for potential limited travel (domestic and international) as needed, to attend Investigator Meetings, project kick-off meetings and/or bid defense meetings
• Fluent in written and verbal English

Pay and benefits

The salary range for this position is USD 50,000.00 to 99,000.00 per year for the United States. The company states that compensation will fall within the provided range, and it is not a guarantee of exact salary. Final salary is determined based on relevant experience, performance, education and internal equity. In addition to base salary, a benefits package is offered depending on location. Salary information will be discussed during the interview process.

About the company

Worldwide Clinical Trials is a global, midsize CRO with over 3,500 experts. The company describes its work as taking pioneering, creative approaches and implementing them with quality and excellence. It states that it is committed to an inclusive and equitable workplace and provides transparent compensation.

Job details

• Req ID: JR102334
• Posted: 2026-07-14
• Employment Type: Full-time
• Work Location: Remote
• Location: United States