ABOUT ABBOTT

At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 110,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.

MAIN PURPOSE OF ROLE

We are seeking a Site-ICRA Intern to join our team. This internship provides hands-on experience in various aspects of clinical research, including document collection, study site activation, maintenance, and close-out. As well as exposure to essential tools such as CTMS and EDC/CRF. The successful candidate will work closely with our experienced team members and gain valuable insights into the clinical research process.

MAIN RESPONSIBILITIES

• Assist in document collection and review.
• Coordinate material shipments and maintain accurate shipment records.
• Contribute to study site maintenance.
• Gain exposure to CTMS (Clinical Trial Management System) for document status tracking.
• Learn to use EDC (Electronic Data Capture) and CRF (Case Report Form) tools.
• Collaborate with cross-functional teams to ensure smooth study execution.

QUALIFICATIONS

• Pursuing a master’s degree in medical studies, biomedical science, or pharmacy.
• Fluent in English (written and spoken).
• Strong organizational skills and attention to detail.
• Ability to work independently and as part of a team.
• Proficiency in Microsoft Excel.
• Quick learner and adaptable to new tools and processes.

WHAT CAN WE OFFER YOU?

Abbott provides a varied, challenging, and international position in a dynamic and pleasant working environment. You will participate in the onboarding process and receive training like that of regular employees.