Offer summary

Qualifications:

Bachelor's degree in Life Sciences or related field., Experience in pharmacovigilance or drug safety is preferred., Strong analytical and communication skills are essential., Familiarity with regulatory requirements in the UK/EU is a plus..

Key responsibilities:

Monitor and assess adverse event reports for compliance.

Prepare and submit safety reports to regulatory authorities.

Collaborate with cross-functional teams to ensure data accuracy.

Participate in meetings with clients to discuss safety data and findings.

About Worldwide Clinical Trials  Worldwide Clinical Trials is a leading full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new treatments. Our capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by our team members who bring their expertise and a collaborative, personalized approach to each clinical program. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers. Our talented team of 3,000+ professionals spans 60+ countries, and embraces a culture of diversity, equity, inclusion, and belonging (DEI&B). We are united in cause with our customers to improve the lives of patients through new, innovative therapies. For more information on Worldwide, visit www.Worldwide.com.

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