Contracts Migration Intern - Fixed Term - Nottingham - Office Based

☞ Worldwide Clinical Trials

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Update day: 07-05-2024

Location: Nottingham East Midlands

Category: Science Labor Pharmaceutical / Chemical / Biotech

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Requisition Number 6951
Employment Type : Fixed Term

Who we are

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.

Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

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 a Contracts Migration Intern does at Worldwide

As a Contracts Migration Intern, you will play a crucial role in ensuring the accuracy and integrity of data before it is imported into our new system. You will work closely with members of the site contracts team, and vendors to support the data cleaning process.

  • Transition site contracts database and documents on to new system
  • Review and verify the accuracy of data collected from various sources. Identify and correct errors, inconsistencies, and missing information in the data.
  • Collaborate with team members to resolve data discrepancies and ensure data integrity.
  • Maintain thorough documentation of migration activities and outcomes.


What you will bring to the role

  • Excellent organizational and time management skills to handle multiple tasks and meet deadlines.
  • Strong problem-solving skills and the ability to work independently and as part of a team.
  • Effective communication skills, both written and verbal.
  • Demonstrated ability to maintain confidentiality and handle sensitive data with integrity.

Your experience

  • Currently enrolled in a Bachelor’s or Master’s degree program in a relevant field (preferred life sciences, data management, statistics, contract management, legal or a related discipline).
  • Strong attention to detail and the ability to spot errors and inconsistencies in data.
  • Proficient in using Microsoft Excel or other data management tools.
  • Familiarity with clinical research terminology and data collection processes is preferred but not required
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Deadline: 21-06-2024

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