Pharmacovigilance Specialist - US - Remote

Worldwide Clinical Trials; Durham (NC); On-site; USD 50,000 - 99,000; Full time

Job summary

Worldwide Clinical Trials is seeking an Associate in Pharmacovigilance in the United States. You will manage SAE data collection, review for completeness, and perform data entry in safety databases, with support from senior PV staff on small to moderate studies.

The role requires a Bachelor’s degree in a science field or nursing, 1 year of PV experience, and strong MS Office skills. You will work in a global environment, travel if needed, and contribute to regulatory safety submissions.

Qualifications

• Bachelor’s degree in a science‑related field, nursing, or equivalent.
• Minimum of 1 year of pharmacovigilance experience (pre‑approval clinical trials).
• Equivalent combination of relevant education and experience.

Responsibilities

• Author Safety Management Plan for assigned studies.
• Review incoming SAE data for completeness and accuracy.
• Perform data entry in the Safety Database and track safety information.

Skills

Medical terminology

Regulatory awareness

Excellent communication

Independent worker

Multi-tasking

Education

Bachelor’s degree in science or nursing

Tools

Excel

PowerPoint

Word

Job description

Who we are

We’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!

What The Associate, Pharmacovigilance Does At Worldwide

Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions.

Serves as Lead PV Associate on small to moderate sized studies that are simple to moderate in complexity and scope of work with support from senior staff.

What You Will Do

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

What You Will Bring To The Role

• Good understanding of medical and scientific terminology, of the principles of clinical assessment of adverse drug events, of international regulations and of reporting requirements
• Good understanding of computer technology, and management of relational database systems, including extraction of data
• Positive attitude and ability to interact diplomatically and professionally with internal and external customers in a global environment
• Excellent organization skills and ability to handle multiple competing priorities within tight timelines
• Consistently demonstrates commitment, dependability, cooperation, adaptability and flexibility in executing 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 (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

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

United States of America - $50,000.00 - $99,000.00

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.