Job Summary
The Senior Clinical Research Coordinator is tasked with the independent oversight of intricate industry-sponsored clinical trials, ensuring that all aspects of the study are effectively executed, regulatory standards are adhered to, and patient enrollment is successful. Additionally, this role involves guiding junior team members, conducting clinical procedures, and maintaining high standards of data management throughout the trial process.
Responsibilities
- Independently manage and execute complex clinical trials sponsored by industry partners.
- Ensure compliance with regulatory requirements throughout the study.
- Oversee patient recruitment efforts to achieve study enrollment milestones.
- Mentor and support junior staff in their roles and responsibilities.
- Conduct clinical procedures as required by the study protocol.
- Ensure the integrity and quality of data management at all stages of the trial.
Qualifications
- Education: Associate’s or Bachelor’s degree in a scientific or healthcare field.
- Experience: Minimum of 5 years in clinical research settings.
- Knowledge of Good Clinical Practice (GCP) and Food and Drug Administration (FDA) regulations.
- Competency in practical clinical tasks such as phlebotomy and performing ECGs.
