Are you a highly skilled leader in clinical data management with a passion for ensuring the integrity, accuracy, and compliance of clinical trial data? We are seeking a Director of Clinical Data Management (Med Device) in Orlando, FL to lead data operations for groundbreaking medical device studies. This role is ideal for a data-driven professional with extensive experience in clinical trial data collection, database management, and regulatory compliance within the medical device sector.
As the Director of Clinical Data Management (Med Device) in Orlando, FL, you will oversee the end-to-end clinical data lifecycle, ensuring data quality, compliance with regulatory requirements, and implementation of best practices in clinical data management. If you thrive in a fast-paced, innovative environment and are committed to delivering high-quality clinical data to support regulatory approvals and market access, we encourage you to apply.
About This Role
The Director of Clinical Data Management (Med Device) in Orlando, FL is responsible for leading all aspects of clinical data management, from study design through database lock, ensuring data integrity, regulatory compliance, and operational efficiency. This role requires collaboration with cross-functional teams, including clinical operations, biostatistics, regulatory affairs, and IT, to develop and maintain robust data management strategies.
As a key leader in the organization, the Director of Clinical Data Management (Med Device) in Orlando, FL will establish and oversee data governance policies, implement innovative data capture technologies, and drive continuous improvements in clinical data processes. With a strong focus on regulatory standards such as FDA, ICH-GCP, and ISO guidelines, this position ensures that all clinical trial data is collected, managed, and reported with the highest level of accuracy and reliability.
Key Responsibilities – Director of Clinical Data Management (Med Device) in Orlando, FL
Develop and Implement Clinical Data Management Strategies
- Design and execute data management plans aligned with regulatory requirements and industry best practices.
- Establish policies and procedures to ensure data integrity, consistency, and compliance across all clinical trials.
- Drive innovation in data capture methodologies, including electronic data capture (EDC) systems and automation tools.
Oversee Data Collection, Cleaning, and Validation Processes
- Lead the setup, testing, and maintenance of EDC systems to ensure accurate data capture.
- Develop and oversee data validation procedures to identify and resolve discrepancies efficiently.
- Implement quality control measures to ensure completeness and reliability of clinical data.
Ensure Compliance with Regulatory and Industry Standards
- Maintain compliance with FDA, ICH-GCP, HIPAA, and other relevant regulatory requirements.
- Collaborate with regulatory affairs teams to ensure accurate and timely submission of clinical data.
- Stay updated on evolving regulations and industry guidelines to align data management practices accordingly.
Manage Clinical Database Design and Maintenance
- Develop and maintain clinical trial databases, ensuring functionality, accuracy, and security.
- Coordinate with IT and biostatistics teams to optimize database structures for efficient data analysis.
- Lead database lock and archival processes to ensure secure long-term data storage.
Lead and Train a High-Performing Clinical Data Management Team
- Recruit, mentor, and develop a skilled team of clinical data management professionals.
- Provide ongoing training and professional development opportunities to enhance team expertise.
- Foster a culture of collaboration, innovation, and continuous improvement in data management.
Collaborate with Cross-Functional Teams to Optimize Clinical Data Operations
- Work closely with clinical operations, regulatory, and statistical teams to streamline data processes.
- Participate in study protocol design to ensure optimal data collection strategies.
- Support risk-based monitoring initiatives by providing real-time data insights.
Drive Efficiency and Innovation in Data Management Processes
- Evaluate and implement new technologies to enhance data collection, analysis, and reporting.
- Optimize workflows to reduce data management cycle times and improve overall efficiency.
- Identify and implement process improvements to ensure high-quality data deliverables.
Support Statistical Analysis and Reporting for Regulatory Submissions
- Ensure clinical data is formatted and structured for biostatistical analysis.
- Oversee the preparation of data listings, tables, and reports for regulatory submissions.
- Collaborate with regulatory and medical writing teams to ensure data accuracy in submission documents.
What The Client is Looking For in You
To excel as the Director of Clinical Data Management (Med Device) in Orlando, FL, you should be a highly experienced professional with deep expertise in clinical data management, regulatory compliance, and leadership. The ideal candidate will possess:
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Extensive Experience in Clinical Data Management – A strong background in overseeing clinical data operations for medical device trials, ensuring data integrity and regulatory compliance.
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Proven Leadership in Data Management Teams – Experience in leading and mentoring high-performing clinical data management teams while fostering a culture of quality, efficiency, and innovation.
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Regulatory & Compliance Expertise – In-depth knowledge of FDA, ICH-GCP, HIPAA, ISO 14155, and other global regulatory requirements governing clinical data in the medical device industry.
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Proficiency in Clinical Data Systems – Hands-on experience with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and other relevant data tools.
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Strategic and Analytical Mindset – Ability to design and implement data strategies that optimize clinical trial efficiency, data quality, and compliance.
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Strong Collaboration & Communication Skills – A track record of working effectively with cross-functional teams, including clinical operations, regulatory affairs, biostatistics, and IT.
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Ability to Drive Process Improvements & Innovation – Passion for enhancing data collection, cleaning, and validation processes through automation, AI-driven insights, and risk-based monitoring approaches.
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Detail-Oriented & Quality-Focused Approach – A meticulous focus on data accuracy, completeness, and adherence to best practices in clinical trial data management.
Why This Opportunity Stands Out
This position offers a unique opportunity to shape the clinical data management function of a fast-growing medical device company. As the Director of Clinical Data Management (Med Device) in Orlando, FL, you will:
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Lead Data Management for Cutting-Edge Medical Devices – Play a key role in clinical trials that bring groundbreaking medical technologies to market.
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Drive Innovation in Clinical Data Processes – Leverage the latest technologies, automation tools, and data management best practices to optimize trial operations.
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Work in a Collaborative & High-Impact Environment – Partner with top professionals across clinical operations, regulatory affairs, and biostatistics to drive data excellence.
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Competitive Compensation & Benefits – Receive a lucrative salary, performance-based incentives, and comprehensive benefits, including healthcare, 401(k), and executive perks.
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Opportunities for Professional Growth – Enhance your career through leadership development, exposure to global clinical trials, and opportunities to shape company-wide data strategies.
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Executive-Level Influence – Be a key decision-maker in the company’s clinical research strategy and play a pivotal role in ensuring compliance and efficiency in clinical data management.
FAQs About the Role
Q: What industries should I have experience in?
A: Candidates should have extensive experience in the medical device industry, specifically in clinical data management for clinical trials. Experience in pharmaceutical or biotech clinical trials is also valuable.
Q: Is relocation required for this position?
A: This role is based in Orlando, FL. Candidates must be open to relocation or already reside in the area.
Q: What is the reporting structure for this role?
A: The Director of Clinical Data Management (Med Device) in Orlando, FL will report directly to the VP of Clinical Operations and work closely with clinical, regulatory, and biostatistics teams.
Q: What kind of leadership style is expected?
A: The company is seeking a strategic, results-driven leader who can foster a culture of collaboration, efficiency, and innovation in clinical data management.
Q: What is the expected travel requirement?
A: This role may require occasional travel for industry conferences, regulatory meetings, and site visits for clinical trial management.
Q: What qualifications and skills are required?
A: Candidates should have a bachelor’s or master’s degree in life sciences, biostatistics, or a related field, along with at least 10+ years of experience in clinical data management. Expertise in EDC systems, regulatory compliance, and team leadership is essential.
Q: How does this role contribute to the company’s overall success?
A: The Director of Clinical Data Management (Med Device) in Orlando, FL ensures that clinical trial data is collected, managed, and reported accurately, which is critical for regulatory approval and successful product commercialization.
Q: What is the timeline for hiring and onboarding?
A: The company is actively seeking the right candidate and aims to complete the hiring process within the next 60–90 days. Onboarding will include collaboration with leadership, an overview of ongoing clinical trials, and integration into the clinical operations team.
What Remuneration Can You Expect from This Job?
As the Director of Clinical Data Management (Med Device) in Orlando, FL, you can expect a highly competitive compensation package that reflects your leadership role and expertise in clinical data management. The base salary typically ranges between $160,000 – $210,000 per year, depending on experience, industry knowledge, and the complexity of past clinical trial oversight.
Beyond the base salary, this role includes performance-based bonuses and incentives tied to key clinical data metrics such as regulatory compliance, data accuracy, and process efficiency improvements. Equity options or stock grants may also be available for the right candidate, offering long-term financial growth.
The benefits package includes comprehensive healthcare coverage (medical, dental, and vision), a 401(k) retirement plan with company matching, paid time off, and executive perks such as travel allowances and conference participation. The company may also offer relocation assistance for candidates moving to Orlando, FL.
This role is a rewarding opportunity to not only receive a lucrative financial package but also to play a pivotal role in shaping the clinical data landscape within a leading medical device organization.
How to Apply for This Director of Clinical Data Management (Med Device) Position in Orlando, FL
If you are a strategic and experienced clinical data management leader looking to drive innovation in medical device trials, we invite you to apply for the Director of Clinical Data Management (Med Device) in Orlando, FL. This is a unique opportunity to lead data operations, optimize clinical trial processes, and contribute to groundbreaking healthcare advancements.
To apply, please submit your resume and a cover letter detailing your experience in clinical data management, regulatory compliance, and leadership within the medical device sector.
This role offers a chance to be at the forefront of clinical data excellence, working in a dynamic, high-impact environment. Apply today to take the next step in your career as the Director of Clinical Data Management (Med Device) in Orlando, FL!
For more information or to explore similar opportunities, visit our Medical Device Recruiters Page.
Tags: Director of Clinical Data Management | Clinical Data Leadership | Medical Device Clinical Trials | Clinical Data Systems | Regulatory Compliance
