Job Description
Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. 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 3,500+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.
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 Medical Writing does at Worldwide Medical Writing at Worldwide is a dynamic global group with comprehensive peer, leadership and administrative support. Our team liaises with Subject Matter Experts across the company, including regulatory strategists and clinical methodologists in high level protocol and clinical development discussions. We also author a wide range of documents across many therapeutic areas.Join us and discover opportunities for ongoing training and career development.
What you will do Tasks may include but are not limited to:
- Prepare study documents such as protocols, informed consent documents, clinical study reports (CSRs), patient narratives, and other documents in accordance with regulatory requirements and WCT SOPs.
- Serve as publishing point-of-contact in conjunction with the document coordinator to publish CSRs or other documents, as needed.
- Create and manage project-specific timelines, adaptation of timing and milestones based on client needs/feedback.
- Identify and appropriately communicate risks associated with document delivery and propose mitigation plans.
What you will bring to the role - Excellent written and spoken English, able to accurately interpret data and express findings in a clear and concise written manner.
- Excellent project/time management and organizational skills, and ability to work independently.
- Flexibility in meeting challenging deadlines and changing requirements while working on multiple projects.
- Attention to detail-style, consistency, grammar, syntax, scientific accuracy.
- Thorough knowledge of applicable regulatory requirements and guidelines (in particular ICH E3, E6, and E9).
Your experience - University/college degree (life science or related allied health profession) and American Medical Writers Association Certification or equivalent combination of education and experience that provides the individual with the required knowledge, skills, and abilities to perform the above responsibilities.
- Graduate degree preferred.
- Minimum of 2 years of clinical pharmaceutical industry experience including skills and competency in medical writing.
- Available for domestic and international travel, including overnight stays (valid passport)
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 ! For more information on Worldwide, visit or connect with us on LinkedIn.
Job Tags
Permanent employment, Contract work, Worldwide, Flexible hours, Night shift,