Transparency and Disclosure Specialist - Serbia - Remote

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 Medical Writing department 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

• Managing and coordinating transparency, anonymization and redaction activities for clinical documents and process submissions
•  Responsible for preparing submission-ready documents to CTIS and any other publicly available portal.
• Responsible for redaction and anonymization of all submission documents for public release
• Contributes to process improvement by refining work instructions, training materials and procedures as needed

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.
• Project/time management and organizational skills, as well as the ability to work independently.
• Understanding of global transparency and disclosure requirements; excellent understanding of all aspects of ICH- GCP, FDA, EMA (CTR and Clinical Trial Information System).
• Attention to detail - style, consistency, grammar, syntax and scientific accuracy.

Your experience

• University/college degree.
  Prior clinical trial, clinical trial regulatory, privacy or pharmaceutical industry experience or equivalent.

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 Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.