Senior clinical research scientist vs study coordinator

Differences between senior clinical research scientist and study coordinator duties and responsibilities

Senior clinical research scientist example responsibilities.

• Supervise and manage planning, implementation, conduct and reporting of assign early phase international clinical studies in oncology.
• Contribute to the development of templates for protocols and clinical study reports following FDA, GCP and ICH guidelines.
• Authore and review abstracts, manuscripts, slide decks and posters in collaboration with internal and external (CRO) stakeholders.
• Lead feasibility and identification of CRO selection for pediatric program.
• Recruit investigators perform pre-study visits, negotiate budgets, initiate and monitor studies and verify data for accuracy and completeness.
• Manage clinical monitors in successful completion of large international hypertension study.

Study coordinator example responsibilities.

• Manage and analyze EKG and sleep data collect from subjects in confidential database.
• Establish and maintain strong community partnerships to achieve HIV prevention objectives.
• Conduct consent discussions and other study procedures per protocol and CFR and GCP guidelines.
• Maintain strict patient confidentiality according to HIPPA regulations, GCP and ICH , 21 CFR and other regulatory documentation.
• Maintain accurate IRB, regulatory and study documentation to insure compliance with protocol and good clinical practice guidelines.
• Coordinate day-to-day study activities including data collection and statistical analysis, protocol development/implementation, IRB relations, and staff development.
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