- 経験
- どれでも
- 給料
- —
- 求人情報
- 1
- 投稿済み
- 1時間前
- 作業モード
- 在任中
- 教育
- University degree in medicine, science or equivalent
- 再開する
- 応募必須
仕事内容
Role Summary
As a Clinical Research Associate I at ICON, you will play a vital role in clinical trial operations, working collaboratively to ensure outstanding results throughout the clinical programs.
Primary Duties
- Independently managing and coordinating all tasks involved in study setup and ongoing monitoring, including preparing precise study status reports and maintaining thorough documentation.
- Efficiently resolving queries generated by sponsors, managing study cost-effectiveness, and assisting in preparing and reviewing documentation and feasibility assessments for new study proposals as necessary.
- Building and nurturing strong, cooperative relationships with stakeholders, clinical investigators, and site personnel.
- Ensuring patient safety by adhering strictly to ICON's protocols, procedures, and all applicable regulatory guidelines.
Candidate Profile
- Holds a university degree in medicine, science, or a related field.
- Thorough understanding of ICH-GCP guidelines with competence in reviewing and assessing medical data.
- Proficient communication skills in English, both written and spoken.
- Interpersonal skills that facilitate prompt and effective query management.
- Prepared to travel as needed, typically between 60% to 75% of the time.