Clinical Associate

Job Summary

Supporting the execution and management of clinical trials, the full-time Clinical Associate will ensure quality and efficiency while working remotely in the field of early development oncology.

Key responsibilities:

• Independently support the planning, execution, and reporting of clinical trials across all phases and therapeutic areas
• Maintain and analyze trial tracking systems to ensure data accuracy and compliance
• Manage the Trial Master File (TMF) and oversee investigational product (IP) and ancillary supply management

Required qualifications:

• Bachelor's degree in a relevant field, such as life sciences or healthcare preferred
• Previous experience in clinical research or a related field preferred
• Strong organizational and communication skills
• Ability to work independently and collaboratively in a fast-paced environment
• Attention to detail and ability to prioritize tasks effectively