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 The Regulatory Affairs Department Does At Worldwide
Regulatory Affairs plays a pivotal role in navigating the complex regulatory landscape, ensuring the success of diverse clinical trials. As subject matter experts, the team leads submissions to regulatory authorities, coordinates with ethics committees across EMEA, Asia Pacific, and Latin America, and ensures compliance with evolving regulations. Their expertise drives the development and approval of innovative medical products, supports business development efforts, and offers strategic guidance on contract negotiations. They also mentor junior staff, review key documentation for global regulatory standards, and keep all stakeholders informed throughout the submission process
What You Will Do
- Training and Development: Participate in training sessions designed to equip the intern with fundamental knowledge about clinical trials and regulatory affairs processes. Gain a deep understanding of the role regulatory affairs plays in the successful execution of clinical studies.
- Collaborative Support: Work closely with experienced Regulatory Affairs specialists and Managers, assisting them in setting up regulatory aspects for clinical trials in diverse global locations. Observe and learn from their expertise in navigating regulatory landscapes and ensuring compliance.
- Document Management: Support the Regulatory Affairs team by organizing document translations, filing important regulatory documents, and tracking their progress. Attention to detail and meticulous record-keeping are essential for this role.
- Team Contribution: Actively participate in team meetings, discussions, and projects. Contribute with ideas and insights, demonstrating curiosity and enthusiasm for the field of regulatory affairs.
- Additional Support: When appropriate, the intern may be invited to assist with other activities within the department, broadening their exposure to various aspects of clinical trial operations.
What You Will Bring To The Role
- Strong interest in clinical research and regulatory affairs.
- Exceptional organizational skills and attention to detail.
- Excellent communication and interpersonal skills.
- Ability to work independently as well as in a team-oriented environment.
- Demonstrated professionalism, curiosity, and a proactive approach to learning.
Your Experience
- Currently enrolled in a Bachelor's or Master's degree program in Life Sciences, Medicine, Pharmacy, Biomedical Sciences, Regulatory Affairs, or related fields.
- Proficiency in MS Office applications (Word, Excel, PowerPoint).
- Fluency in English language, both written and verbal
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
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