Clinical Research Coordinator IV managing complex clinical trials and supervising research administration staff. Handling compliance, budgets, and participant engagement strategies in a healthcare setting.
About the role
- Clinical Scientist supporting the execution of clinical trials at Oruka Therapeutics. Involves operational support, data collection, and cross-functional collaboration in clinical development.
Responsibilities
- The Clinical Scientist plays a key role in the execution and operational support of clinical trials, assisting in the collection and review of clinical data to ensure study success.
- This role involves supporting protocol development, study implementation, data review, and documentation preparation to align with clinical development goals.
- The Clinical Scientist collaborates closely with cross-functional teams to ensure the generation of high-quality clinical data.
- Additionally, they work closely with the Medical Director, Clinical Development to execute key tasks.
- Contributes to the development of clinical trial protocols, including patient selection criteria, study endpoints, and data collection methods.
Requirements
- Advanced degree in life sciences, such as a PhD, PharmD or related field
- Understanding of clinical trial methodologies and regulatory requirements
- Experience in clinical study design, data analysis, data review and interpretation
- Good written and verbal communication skills
- Ability to work effectively in a collaborative, cross-functional environment.
Benefits
- A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients.
- Competitive salary and benefits package.
- A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work.
- Opportunities for professional growth and development.
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