Job Summary
A company is looking for a Director Clinical Scientist Consultant.
Key Responsibilities
- Develop clinical concepts and plans, including writing protocols and informed consent forms
- Collaborate with Clinical Operations on site selection and communication, and represent the medical function on clinical study teams
- Author clinical study reports, manage safety data, and support Health Authority interactions
Required Qualifications
- Bachelor's degree with strong knowledge of clinical oncology; training in immuno-oncology is desired
- Postgraduate qualification in clinical oncology (e.g., Master's degree), MD, Nurse Practitioner License, PharmD, or PhD is welcomed
- At least 2 years of industry experience in oncology, preferably in early phase clinical trials
- Experience in protocol design, medical monitoring, and assessment of adverse events in clinical trials
- Knowledge of Good Clinical Practice and fluency in English is required
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