Job Title:
Associate, Pharmacovigilance
Location:
Remote – United States
Company:
Worldwide Clinical Trials
Compensation:
Competitive (not specified in the job description)
Job Summary
Worldwide Clinical Trials is hiring a Pharmacovigilance Associate to join their remote team in the United States. This is an excellent opportunity for professionals with at least 1 year of PV experience in pre-approval clinical trials to contribute to global drug safety operations. You’ll be part of a forward-thinking, midsize CRO known for innovation, scientific rigor, and a patient-centric approach to clinical development.
Key Responsibilities
Author Safety Management Plans for assigned studies
Attend and present in internal, client, and Investigator Meetings
Review Serious Adverse Events (SAEs) for accuracy and completeness
Enter safety data into the database and maintain tracking records
Query and follow up with clinical sites for missing safety data
Perform Quality Control checks on processed SAEs
Generate regulatory reports and perform safety submissions
Prepare and submit periodic safety reports
Stay up-to-date with safety regulations and guidelines
Monitor project scope and escalate issues as needed
Assist in bid defenses, training, or mentoring new PV staff
Required Skills & Qualifications
Bachelor's degree in a science-related field, nursing, or equivalent
Minimum 1 year of pharmacovigilance experience (pre-approval trials)
Familiarity with medical terminology, clinical AE assessment, and global PV regulations
Proficiency in MS Office (Excel, PowerPoint, Word)
Strong written and verbal communication skills
Detail-oriented with excellent organizational abilities
Capable of managing multiple priorities within deadlines
Comfortable working independently and in a matrix team environment
Willingness to travel occasionally for meetings (domestic/international)
Fluent in English (written and spoken)
Perks & Benefits
100% Remote work flexibility within the US
Work with innovative, science-driven CRO projects
Inclusive and supportive workplace culture
Career development and cross-functional collaboration opportunities
Opportunity to support global regulatory submissions and drug safety
Company Description
Worldwide Clinical Trials is a global, mid-sized Contract Research Organization (CRO) with over 3,500 experts delivering high-quality clinical development services. Focused on innovation and therapeutic impact, Worldwide is a leader in patient-centric trials and drug safety operations, partnering with sponsors to advance medical breakthroughs.
Work Mode
Remote – USA
Call-to-Action
Ready to make a difference in global drug safety? If you’re passionate about pharmacovigilance and seeking a flexible, mission-driven role, apply now and become part of a company that’s reimagining the future of CROs.
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