Clinical Scientist
Behavioral Health Market Context
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Job Description
ead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights that move programs forward.
Responsibilities:
• Lead design and execute clinical deliverables to support the CDP, including INDs, protocols, IBs, and study documents (CRFs, SAPs, data listings).
• Oversee clinical data generation, validation, and review, including query resolution, patient eligibility, and protocol deviation management.
• Perform study subject-level data analysis to inform clinical development strategy and reporting.
• Partner with medical teams, advisors, and Health Authorities, including support for HA/IRB interactions and responses.
• Contribute to therapeutic area research, KOL/investigator engagement, and development of scalable clinical processes.
Qualifications:
• A minimum of 8 years of relevant experience and an advanced degree (PharmD, PhD, MD, MSN, PA, MPH, etc.)
• Strong background in small molecule therapies and oncology clinical development.
• Experience in hematology required.
• Experience in early phase clinical trials required.
Responsibilities:
• Lead design and execute clinical deliverables to support the CDP, including INDs, protocols, IBs, and study documents (CRFs, SAPs, data listings).
• Oversee clinical data generation, validation, and review, including query resolution, patient eligibility, and protocol deviation management.
• Perform study subject-level data analysis to inform clinical development strategy and reporting.
• Partner with medical teams, advisors, and Health Authorities, including support for HA/IRB interactions and responses.
• Contribute to therapeutic area research, KOL/investigator engagement, and development of scalable clinical processes.
Qualifications:
• A minimum of 8 years of relevant experience and an advanced degree (PharmD, PhD, MD, MSN, PA, MPH, etc.)
• Strong background in small molecule therapies and oncology clinical development.
• Experience in hematology required.
• Experience in early phase clinical trials required.
Qualifications
- •A minimum of 8 years of relevant experience and an advanced degree (PharmD, PhD, MD, MSN, PA, MPH, etc.)
- •Strong background in small molecule therapies and oncology clinical development
- •Experience in hematology required
- •Experience in early phase clinical trials required
Benefits
Responsibilities
- •Summary: The Clinical Scientist will lead aspects of protocol development, study planning, data generation, analysis, and reporting as well as work cross-functionally to deliver high-quality data and insights that move programs forward
- •Lead design and execute clinical deliverables to support the CDP, including INDs, protocols, IBs, and study documents (CRFs, SAPs, data listings)
- •Oversee clinical data generation, validation, and review, including query resolution, patient eligibility, and protocol deviation management
- •Perform study subject-level data analysis to inform clinical development strategy and reporting
- •Partner with medical teams, advisors, and Health Authorities, including support for HA/IRB interactions and responses
- •Contribute to therapeutic area research, KOL/investigator engagement, and development of scalable clinical processes
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