Freelance Oncology Research Specialist
4 weeks ago
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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