Senior Associate, Pharmacovigilance

Worldwide Clinical Trials; Brasília; Remote; BRL 120,000 - 180,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Associate Pharmacovigilance for a remote Brazil role. You will lead PV activities on small to moderate studies, author Safety Management Plans, review SAE data, and ensure timely regulatory submissions in collaboration with global teams. The role demands a science degree, 1 year PV experience, strong communication, and English fluency; travel as needed.

Qualifications

• Bachelor’s degree in a science-related field is required.
• Minimum of 1 year pharmacovigilance experience in clinical trials.
• Proficient in MS Office (Excel, PowerPoint, Word).
• Excellent written and verbal communication; detail-oriented.
• Ability to work independently and in a matrix team environment.
• Fluent in written and verbal English.

Responsibilities

• Lead pharmacovigilance activities for small to moderate-sized studies.
• Author Safety Management Plans for assigned studies.
• Review SAE data for completeness and regulatory compliance.
• Enter and maintain safety information in safety databases.
• Prepare safety reports and support submissions.
• Ensure PV activities comply with regulations and SOPs.
• Coordinate with global teams and external partners.

Skills

Excellent communication skills

Strong organizational skills

Ability to prioritize multiple tasks

Independent work in matrix environment

Fluent in English

Education

Bachelor’s degree in a science-related field

Tools

MS Office Suite

Job description

Who We AreWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

Who We AreWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! 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. 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

We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn. Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.