Offer summary

Qualifications:

Bachelor's degree in Life Sciences or related field., Minimum of 5 years of experience in clinical research., Strong knowledge of GCP and regulatory requirements., Excellent communication and organizational skills..

Key responsibilities:

Oversee and manage clinical trial sites to ensure compliance.

Conduct monitoring visits and prepare detailed reports.

Collaborate with cross-functional teams to support study objectives.

Provide training and guidance to site staff on study protocols.

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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