VP of Clinical Affairs – Vascular Device Trials | Miami, FL

Are you a strategic clinical leader with deep expertise in vascular device trials and a passion for advancing innovative medical technologies? We are seeking a Vice President of Clinical Affairs to lead and oversee clinical trial operations for cutting-edge vascular devices. Based in Miami, FL, this is a unique opportunity to drive clinical excellence, regulatory compliance, and impactful data generation within a pioneering medical device company. If you excel in leading multidisciplinary teams and shaping clinical strategy in a fast-evolving environment, we want to hear from you.

Lead Clinical Strategy and Execution for Vascular Device Innovation

Join a forward-thinking medical device company in Miami, FL as the Vice President of Clinical Affairs, where you will spearhead clinical trials and regulatory collaborations for vascular devices. The ideal candidate will bring extensive experience in clinical trial design, execution, and oversight, combined with a thorough understanding of FDA and global regulatory pathways. If you are passionate about transforming vascular care through evidence-based clinical research and have a track record of leading high-impact clinical programs, this role offers a platform to make a significant difference in patient outcomes and company growth.

Key Responsibilities of the Vice President of Clinical Affairs – Vascular Device Trials

Clinical Strategy & Leadership: Develop and execute comprehensive clinical strategies that align with company goals and regulatory requirements. Lead the design, planning, and oversight of vascular device clinical trials to generate robust data supporting product approvals and market access.

Trial Management & Execution: Oversee all phases of vascular device clinical trials, ensuring timelines, budgets, and quality standards are met. Collaborate with clinical operations teams, investigators, and external partners to drive trial efficiency and patient safety.

Regulatory & Compliance Oversight: Ensure all clinical activities comply with FDA, EMA, and other global regulatory bodies’ requirements, as well as Good Clinical Practice (GCP) guidelines. Lead the preparation and submission of regulatory documents and clinical trial applications.

Data Integrity & Quality Assurance: Implement rigorous clinical data management processes and quality assurance practices to ensure integrity and reliability of trial results. Work closely with biostatistics, medical affairs, and regulatory teams to interpret clinical data.

Cross-Functional Collaboration: Partner with R&D, regulatory affairs, marketing, and commercial teams to integrate clinical insights into product development, regulatory strategy, and commercialization plans.

Team Development & Leadership: Build and mentor a high-performing clinical affairs team, fostering a culture of scientific excellence, accountability, and continuous improvement.

Stakeholder Engagement: Serve as the clinical affairs liaison to external stakeholders including key opinion leaders, clinical investigators, and regulatory agencies. Represent the company at industry conferences, advisory boards, and clinical consortiums.

Risk Management & Ethical Standards: Identify and mitigate clinical trial risks, ensuring patient safety and ethical conduct of clinical research. Establish policies and procedures that promote compliance and risk reduction.

What the Client is Looking for in You

As the Vice President of Clinical Affairs for Vascular Device Trials, the client seeks a highly skilled clinical leader with a proven record of successfully managing complex clinical programs in the medical device space. You should be a strategic, results-oriented professional who thrives in fast-paced environments and can lead clinical innovation while ensuring regulatory compliance and patient safety.

Proven Expertise in Vascular Device Clinical Trials

The ideal candidate will bring extensive experience in vascular or cardiovascular device clinical trial management. You should have a demonstrated history of designing and executing clinical studies that meet stringent regulatory standards and generate high-quality data to support product approvals and market access.

Strategic Clinical Vision and Regulatory Insight

You must have the ability to develop and implement long-term clinical strategies that align with business goals and evolving regulatory landscapes. The client values leaders who can anticipate regulatory changes, leverage clinical data to inform product development, and drive evidence-based decision-making.

Strong Leadership and Team Building Skills

Leadership excellence is critical for this role. You should be adept at building, mentoring, and leading high-performing clinical teams, fostering collaboration across departments, and driving accountability and scientific rigor in clinical operations.

In-Depth Knowledge of Regulatory and Compliance Standards

A thorough understanding of FDA, EMA, and global regulatory requirements for vascular devices is essential. The client expects a leader who can ensure full compliance with Good Clinical Practice (GCP) and manage clinical risk effectively to safeguard patient welfare and data integrity.

Collaborative and Influential Communicator

The ability to engage effectively with cross-functional teams, key opinion leaders, regulatory agencies, and external clinical investigators is vital. Strong interpersonal skills and credibility within the vascular device clinical community will enable you to represent the company confidently at scientific and industry forums.

Commitment to Innovation and Patient-Centric Research

Finally, the client seeks a visionary clinical affairs leader who is passionate about advancing vascular health through innovative clinical research. You should be committed to conducting patient-centric trials that not only meet regulatory standards but also improve clinical outcomes and quality of life.

FAQs About the Role – Vice President of Clinical Affairs – Vascular Device Trials

What are the key responsibilities of the VP of Clinical Affairs in this role?

As the Vice President of Clinical Affairs, you will lead the planning, execution, and oversight of vascular device clinical trials. You will develop clinical strategies, ensure regulatory compliance, manage clinical teams, collaborate with cross-functional departments, and engage with external investigators and regulatory agencies to support product approvals and market access.

What qualifications and experience are required for this position?

The ideal candidate will have extensive experience managing clinical trials for vascular or cardiovascular devices, strong knowledge of FDA and global regulatory requirements, and proven leadership in clinical operations. An advanced degree in life sciences, medicine, or a related field is preferred, along with expertise in Good Clinical Practice (GCP) and clinical data management.

What leadership qualities are essential for this role?

The client seeks a strategic, results-driven leader with excellent communication and team-building skills. You should be able to inspire multidisciplinary teams, foster collaboration, and maintain a patient-centric approach while driving scientific rigor and regulatory compliance throughout clinical development.

What challenges can I expect in this role?

Challenges include managing complex, multi-site clinical trials within tight timelines and budgets, navigating evolving regulatory landscapes, ensuring high data quality and patient safety, and aligning clinical activities with business objectives in a competitive medical device environment.

What impact is the VP of Clinical Affairs expected to have on the company?

You will play a critical role in advancing the company’s vascular device pipeline by generating pivotal clinical evidence, enabling regulatory approvals, and supporting successful product commercialization. Your leadership will directly influence patient outcomes and the company’s market position.

What is the company’s culture and work environment like?

The company promotes a collaborative, innovation-driven culture focused on patient-centric solutions and scientific excellence. You will join a dynamic team committed to advancing vascular health through cutting-edge medical device research and development.

What Remuneration Can You Expect from This Job?

As the Vice President of Clinical Affairs for Vascular Device Trials in Miami, FL, you can expect a competitive and comprehensive compensation package designed to attract experienced clinical leaders in the medical device industry. The remuneration typically includes:

Base Salary

The base salary for a VP of Clinical Affairs in the vascular device sector varies depending on company size, clinical pipeline, and market presence. For mid-to-large medical device companies, the annual base salary generally ranges from $180,000 to $300,000, with potential for higher compensation in leading organizations.

Performance-Based Bonuses

In addition to the base salary, most compensation packages include annual performance bonuses tied to clinical milestones, regulatory achievements, budget adherence, and overall contribution to the company’s clinical and commercial success. These bonuses can range from 20% to 50% of the base salary.

Equity & Stock Options

Many companies offer equity incentives such as stock options or restricted stock units (RSUs) to align your interests with the company’s long-term growth. Depending on company valuation and stage, equity can form a meaningful portion of the total compensation package.

Long-Term Incentive Plans

Some organizations provide long-term incentive plans (LTIPs) that reward sustained clinical development success and company growth over multiple years. These plans encourage commitment and align with strategic clinical and business goals.

Executive Benefits & Perks

The role typically comes with a comprehensive benefits package, including:

Health, dental, and vision insurance
Retirement savings plans with company matching
Flexible work arrangements
Professional development opportunities
Travel and conference allowances related to clinical affairs activities

Signing Bonuses & Relocation Assistance

For exceptional candidates, companies may offer signing bonuses or relocation support to facilitate transition to the Miami area. These incentives vary based on experience and company policy.

Total Compensation Potential

Taking into account base salary, bonuses, equity, and benefits, total compensation for this VP-level clinical affairs position can range from approximately $220,000 to $400,000 annually, with higher packages available at leading or publicly traded vascular device firms.

How to Apply

If you are a visionary and results-oriented clinical leader with a strong background in vascular device trials, we invite you to apply for the Vice President of Clinical Affairs position in Miami, FL. This is a unique opportunity to lead critical clinical development programs, influence regulatory strategy, and drive innovation in a fast-evolving medical device industry.

To apply, please submit your updated resume along with a cover letter highlighting your experience in managing vascular or cardiovascular clinical trials, regulatory compliance, clinical operations leadership, and cross-functional team management. Emphasize your proven ability to deliver clinical evidence that supports product approvals and market success.

This role offers a high-impact career opportunity to shape the future of vascular device development and improve patient outcomes through strategic clinical leadership. Apply today to take the next step in your executive clinical affairs career as Vice President of Clinical Affairs – Vascular Device Trials in Miami, FL!

For more information or to explore similar executive opportunities in medical devices and clinical development, visit our Executive Healthcare Recruiters Page.

Job Category: Vascular Device Trials

Job Type: Full Time

Job Location: Miami

VP of Clinical Affairs – Vascular Device Trials | Miami, FL