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Clinical Trials Associate - Serbia/UK

Serbia full-time Entry Salary not listed
full-time Entry level Technology & IT Curated
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About the role

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 does a Clinical Trials Associate do at Worldwide

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

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 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.
Originally posted on Himalayas

Interview prep

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Entry
Technology & IT Excel Writing Clinical Trials Associate Entry level

Likely questions

  1. Tell us about work you have done that is close to the Clinical Trials Associate - Serbia/UK role.
  2. How would you approach your first 30 days at name?
  3. Which of Excel, Writing and Clinical have you used recently, and what did it help you achieve?
  4. What have you learned quickly in a past role, project, or training experience?
  5. How do you handle busy days, changing priorities, or pressure at work?

Prepare before the call

  • A recent example that proves your experience with Excel, Writing and Clinical.
  • One short story with a problem, your action, and the result.
  • Two examples that show the strengths listed on your CV.
  • A clear reason why this role and company interest you.
  • Your availability, preferred work style, and salary expectations.

Ask them

  • What would success look like in the first 90 days?
  • What are the main problems this hire should help solve?
  • How does the team give feedback and measure good work?
  • What does a normal working week look like for this role?
Practice line

I am interested in the Clinical Trials Associate - Serbia/UK role because I can bring practical experience in Excel, Writing and Clinical, learn the team quickly, and contribute to the outcomes name needs from this hire.

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