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You will support Clinical Trial Management Associates and Clinical Research Associates by managing trial documentation and maintaining the Trial Master File. Additionally, you will perform data entry, maintain operational trackers, and prepare reports to support clinical trial updates.
Are you a passionate Life Sciences student looking to gain hands-on experience in the fast-paced world of clinical trials? We are partnering with an innovative biotechnology company dedicated to developing groundbreaking, high-impact therapies for patients with severe medical conditions. Operating on a global scale, our client combines cutting-edge scientific research with a collaborative culture that values continuous learning and innovation. By joining their clinical team, you will work alongside experienced professionals and directly contribute to advancing life-saving treatments.
In this role, you will play a crucial part in supporting Clinical Trial Management Associates (CTMAs) and Clinical Research Associates (CRAs) to keep trial operations running smoothly.
Documentation Management: Track trial documentation, conduct Trial Master File (TMF) activities (uploading, indexing, and quality verification), and ensure compliance with regulatory standards.
System & Data Entry: Accurately enter and maintain critical trial data across internal systems and maintain operational trackers.
Reporting: Prepare operational reports and presentation materials to support clinical trial updates.
Monitoring Support: Assist Clinical Research Associates (CRAs/monitors) with daily administrative and operational duties.
Education: Active student status required, preferably pursuing a degree in Pharmacy, Biotechnology, Chemistry, Physics, or related Life Sciences fields.
Technical Skills: Proficiency in MS Office (Excel, PowerPoint), familiarity with graphic design tools like Canva, and a practical understanding of AI tools.
Language Proficiency: Good command of English (minimum B2 level) for effective everyday communication.
Soft Skills: Excellent organizational abilities, strong attention to detail, proactive attitude, and clear communication skills.
Gain practical, real-world experience in the clinical research industry.
Mentorship from seasoned industry professionals.
Flexible working environment tailored around your university schedule (100% remote, 30 hours per week)
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