Senior Associate - Pharmacovigilance (Brazil/UK)

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.
With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research.
Make an Impact as a Senior Associate Pharmacovigilance at Worldwide
Play a critical role in patient safety by ensuring the accurate collection, evaluation, and reporting of serious adverse event (SAE) data for clinical trials. Your work will help support regulatory compliance while contributing to the development of therapies that can improve lives around the world.
As a Senior Associate Pharmacovigilance, you'll take ownership of key pharmacovigilance activities, collaborate with global study teams, and serve as the Lead PV Associate on small to moderate-sized studies. This is an opportunity to apply your scientific knowledge, attention to detail, and problem-solving skills in a fast-paced, quality-focused environment.
Working closely with internal stakeholders and external partners, you'll help ensure safety data is processed accurately, timelines are met, and reporting requirements are fulfilled to the highest standards
Where You'll Work
This is a remote role open to candidates based in Brazil/UK. You will collaborate with global teams across multiple time zones. Limited domestic and international travel may be required for investigator meetings, project kick-off meetings, and/or bid defense meetings.
What You'll Do
Lead pharmacovigilance activities for small to moderate-sized clinical studies with support from senior team members
Author Safety Management Plans for assigned studies to support effective safety oversight
Review incoming SAE data for completeness, accuracy, and regulatory compliance
Enter and maintain safety information within safety databases and tracking systems
Generate and manage follow-up queries to resolve missing, incomplete, or unclear safety information
Perform quality control reviews of SAE cases processed by other Pharmacovigilance Associates
Prepare regulatory safety reports and support timely safety submissions
Ensure all pharmacovigilance activities are conducted in accordance with applicable regulations, SOPs, and study-specific requirements
What You'll Bring
Bachelor’s degree in a science-related field, nursing, or an equivalent combination of education and relevant experience
Minimum of 1 year of pharmacovigilance experience supporting 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 matrix team environment
Ability and willingness for potential limited travel (domestic and international) as needed (attend Investigator Meeting, project kick-off meeting and/or bid defense meeting)
Fluent in written and verbal English
Discover the Difference
We love knowing that someone is going to have a better life because of the work we do. Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit http://www.worldwide.com/careers, or connect with us on LinkedIn.

Work arrangement
Yes