Offer summary

Qualifications:

Bachelor's degree in life sciences or related field., Proven experience in medical writing, particularly in regulatory submissions., Strong understanding of clinical research and medical terminology., Excellent communication and organizational skills..

Key responsibilities:

Develop and write high-quality clinical documents including protocols and clinical study reports.

Collaborate with cross-functional teams to ensure accuracy and compliance of documents.

Review and edit documents for clarity, consistency, and adherence to guidelines.

Participate in meetings with clients and stakeholders to discuss project requirements.

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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