Clinical Research Expert for Solid Tumors
2 weeks ago
About the Role
">We are seeking a skilled Clinical Research Expert to join our Solid Tumors team. In this role, you will be responsible for leading or co-leading clinical trials in a therapeutic area for one or more compounds.
Your Key Responsibilities
">- Develop and implement clinical trial strategies, working closely with cross-functional teams to ensure timely deliverables.
- Collaborate with Medical Directors and other Clinical Research Scientists to achieve program goals.
- Contribute to the development of clinical development plans, study protocols, and regulatory documents.
- Provide medical input for country/site selection, feasibility assessment, and key opinion leader interaction.
- Assist in training investigators, sites, and CRO/CRA as warranted.
- Develop and review clinical and regulatory documents, including protocol, ICF, IB, annual safety updates, and study reports.
- Participate in the development of case report forms and their completion guidelines.
About You
">- You have a PhD, Pharm D, MS, or equivalent degree in a related discipline.
- You possess minimum 6 years of experience in clinical research, with at least 3 years in drug development.
- Prior oncology/hematology drug development experience is highly valued.
- You demonstrate proven skills in project-oriented matrixed team environments.
- Excellent oral, written, and interpersonal communication skills are essential.
- You can travel as needed.
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