Are you an experienced operations professional with a passion for managing clinical trials? Join our esteemed client, a major Healthcare Firm based in Miami, FL, as a Clinical Trials Operations Manager. We are searching for a dedicated leader to oversee the planning, execution, and management of clinical trials, ensuring adherence to regulatory standards and operational excellence.
About Our Client:
Our client is a leader in the healthcare industry, committed to advancing medical research and improving patient outcomes. With a focus on conducting high-quality clinical trials, they are at the forefront of innovation in healthcare. As they continue to grow, they are looking for a skilled Clinical Trials Operations Manager to ensure the smooth execution of clinical studies and contribute to the future of healthcare research.
Responsibilities of the Clinical Trials Operations Manager:
As the Clinical Trials Operations Manager, you will be responsible for:
- Clinical Trial Oversight: Leading the planning, coordination, and execution of clinical trials, ensuring they are completed on time and within budget.
- Regulatory Compliance: Ensuring all clinical trial activities comply with FDA, ICH-GCP, and other applicable regulations and guidelines.
- Team Management: Overseeing clinical trial staff, including coordinators, data managers, and other support personnel, to ensure efficient trial operations.
- Budget Management: Managing clinical trial budgets, ensuring cost-effective use of resources while maintaining the highest standards of quality.
- Vendor Coordination: Collaborating with external vendors, such as CROs and lab partners, to ensure timely and accurate execution of clinical trial activities.
- Data Integrity: Ensuring the integrity and quality of data collected during clinical trials, facilitating smooth data analysis and reporting.
Qualifications:
To succeed in the role of Clinical Trials Operations Manager, you should possess:
- Experience: Proven experience in clinical trial operations management, preferably within the healthcare or pharmaceutical industries.
- Regulatory Knowledge: Strong understanding of FDA regulations, ICH-GCP guidelines, and clinical trial protocols.
- Leadership Skills: Excellent leadership and communication skills, with the ability to manage cross-functional teams and engage with external stakeholders.
- Analytical Skills: Strong problem-solving and analytical skills, with a focus on ensuring the accuracy and quality of clinical data.
- Educational Background: A bachelor’s degree in Life Sciences, Healthcare Management, or a related field is required. Advanced degrees and certifications (e.g., CCRA, CCRP) are highly desirable.
How to Apply:
If you are a detail-oriented and dedicated professional ready to drive the success of clinical trials, we encourage you to submit your resume and a cover letter outlining your qualifications and vision for the role.
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