At a Glance
- Tasks: Support clinical project teams with administrative tasks and project tracking.
- Company: Join a global CRO dedicated to innovative healthcare solutions.
- Benefits: Remote work, diverse culture, and opportunities for personal growth.
- Other info: Inclusive environment that values creativity and collaboration.
- Why this job: Make a real difference in patients' lives while developing your career.
- Qualifications: Degree or equivalent experience with strong organisational skills.
The predicted salary is between 27000 - 33000 £ per year.
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.
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.
As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.
What you will do:
- Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
- Maintain and quality audit to assure the most recent revisions of documents are on project portals
- Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File
- Maintain version and quality control of project documentation and submit to trial master file
- Assist with the tracking and maintenance of project related information, including site medical question and answer log
What you will bring to the role:
- Excellent written and verbal English as well as fluency of the language of the country of location
- Ability to handle multiple tasks and exercise independent judgment
- Strong attention to detail and focus on quality of work
- Strong organizational and problem-solving skills
- Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Your experience:
- Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
- Skill sets and proven performance equivalent to the above
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.
Clinical Trials Associate - UK or Serbia - Remote employer: Worldwide
At Worldwide Clinical Trials, we pride ourselves on being an exceptional employer that fosters a culture of innovation and collaboration. Our remote work model allows for flexibility while our commitment to diversity and inclusion ensures that every team member can thrive and contribute meaningfully to our mission of improving lives. With ample opportunities for professional growth and a supportive environment, we empower our employees to take charge of their careers and make a real impact in the clinical research field.