Assistant Clinical Research Coordinator
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 Assistant Clinical Research Coordinators do at Worldwide
Clinical Research Coordinator Supervisor, and each clinical trial’s Principal Investigator, is responsible for assisting with assuring that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines and ICH guidelines as applicable.
Teamwork and collaboration is paramount, especially as a globally distributed, remote based team. We are at the forefront of Worldwide’s exciting growth and the nexus between candidates and opportunities.
What you will do- Always represent Worldwide Clinical Trials Early Phase Services (WCTEPS) in a professional manner (verbal, written and in appearance) when interacting with Sponsors, subjects, outside vendors and fellow employees.
- Review study protocol for studies as assigned.
- Attend study initiation visits for their studies.
- During involvement in trial, helps assure source documents for the trial are accurate and thorough.
- Performs data transcription and maintenance of paper study and source documents .
- Strong interpersonal and communication skills.
- Ability to understand written and oral instructions.
- Basic computer knowledge and applications required for generation of business correspondence and preparation of regulatory and other study documents.
- A Bachelor’s degree and a minimum of one year of relevant experience working in an administrative or support capacity required OR an equivalent combination of education and exp organizational skills.
- Ability to meet deadlines with high quality work experience.
- An understanding of scheduling across multiple time zones preferred
- Experience in a related industry such as healthcare, pharmaceutical, or clinical research preferred
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 www.worldwide.com/careers ! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn .