Freelance Oncology Research Specialist

4 weeks ago


London, Greater London, United Kingdom Meet Full time

Meet is seeking an experienced Freelance Clinical Research Associate (CRA) to join our team. This full-time engagement requires extensive experience in oncology clinical trials, strong project management skills, and a passion for advancing medical research. The ideal candidate will be detail-oriented, have a deep understanding of oncology protocols, and excel in a dynamic, fast-paced environment.

Key Responsibilities:

  • Monitor and manage clinical trial sites to ensure compliance with protocols, regulatory guidelines, and study timelines in oncology-focused trials.
  • Conduct on-site visits, monitoring, and audits to ensure the success of the study.
  • Collaborate closely with the project team to ensure the timely completion of the study.
  • Collect, review, and manage clinical trial data to ensure accuracy and completeness, adhering to Good Clinical Practice (GCP) guidelines.

Qualifications:

  • Minimum 3 years of experience as a Clinical Research Associate (CRA) with a strong background in oncology.
  • Excellent communication and interpersonal skills, with the ability to work independently and manage multiple clinical sites.
  • Strong knowledge of ICH-GCP guidelines and regulatory requirements.
  • Ability to work in a fast-paced environment and prioritize tasks effectively.


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