Clinical Operations Intern
TypeInternship
LocationPoland
Posted17 hours ago
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.
Key Responsibilities
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.
Candidate Profile
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.
What's in It for You?
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)
Originally posted on Himalayas
Key Responsibilities
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.
Candidate Profile
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.
What's in It for You?
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)
Originally posted on Himalayas
Apply on Himalayas →
Job sourced from Himalayas. Applications happen directly on the original platform — we never collect your data.