Job Description
Full job description
Avania Clinical is a leading contract research organization (CRO) that offers exciting career opportunities for professionals in the clinical research industry. With a global footprint, a diverse range of therapeutic areas, and expertise in supporting medical device and MedTech solutions, Avania Clinical provides a dynamic and rewarding work environment that fosters growth, innovation, and collaboration.
Join our team of subject matter experts and contribute to the development of life-changing medical devices that improve patients' lives worldwide.
Avania are Hiring – Vice President - Regulatory and Advisory Services
Avania is adding to our dynamic, multi-disciplinary Regulatory and Advisory Services team. We are seeking an experienced regulatory professional with deep expertise in medical device regulatory strategy, particularly with the U.S. FDA. This is a senior-level technical role for a regulatory expert who brings strategic insight, hands-on regulatory experience, and a proven ability to guide medical device companies through complex regulatory landscapes.
In the role of VP role, you will engage with potential new clients to understand their products and needs, design client support programs, lead client engagements, shape regulatory strategies for novel technologies, negotiate with regulators such as FDA, and provide expert guidance throughout the product lifecycle—from development through submission and post-market activities.
The role of Principal Consultant will involve the following;
General Responsibilities:
Own the overall client strategy.
Service as trusted advisor and strategist, helping clients solve their most critical business challenges.
Strong ability to synthesize all details, including client business needs, to produce a comprehensive strategy.
Ability to articulate complex concepts in a simple way which can be understood by cross-functional stakeholders.
Lead and direct client projects, ensuring strategic alignment and successful delivery.
Act as point of contact with regulatory authorities (e.g. FDA, Notified Body, TGA etc) as needed for the client.
Client Management:
Manage client accounts and maintain strategic, long-term relationships with
key client decision-makers.
Ability to interact with Senior level client personnel, Board of Directors, and Investors.
Ensure client’s best interests are represented at all times, balancing client needs with Avania’s capabilities.
Act as a bridge between the client’s executive team and the consulting team.
Handle complex or high-risk issues that may arise within the project, stepping in when there are significant problems or disputes to resolve.
Business Development:
Participate in new opportunity scoping calls, provide technical strategic input, craft proposals to support client needs, negotiate contracts.
Generate new business by identifying opportunities within existing accounts, proposing new services or solutions, and negotiating contracts.
Represent Avania in thought leadership activities, such as speaking at conferences or publishing articles, which can enhance Avania’s reputation and brand
This is an individual contributor role
The ideal candidate will have prior experience working at the FDA, combined with a strong understanding of regulatory requirements across multiple global markets, including the EU MDR, UK, Canada, and Australia. Experience working as a regulatory consultant or within a company developing a novel medical device is highly desirable.
We offer -
The opportunity to work in an innovative, fast-growing and rewarding industry
A dynamic and enthusiastic global team that fosters collaboration and the opportunity to work with experts across many specialties
Exchange of knowledge and ideas to help employees grow and advance their careers, backed with training and other development opportunities
Competitive compensation and benefits package (details shared during the interview process)
Some roles offer the opportunities for travel
Ask us about our hybrid and fully remote work opportunities
We look forward to receiving your application!
Avania takes pride in being an equal opportunity employer. We consider qualified applicants without regard to race, color, religion, gender, national origin, age, ****** orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
#LI-DNI
Avania Clinical is a leading contract research organization (CRO) that offers exciting career opportunities for professionals in the clinical research industry. With a global footprint, a diverse range of therapeutic areas, and expertise in supporting medical device and MedTech solutions, Avania Clinical provides a dynamic and rewarding work environment that fosters growth, innovation, and collaboration.
Join our team of subject matter experts and contribute to the development of life-changing medical devices that improve patients' lives worldwide.
Avania are Hiring – Vice President - Regulatory and Advisory Services
Avania is adding to our dynamic, multi-disciplinary Regulatory and Advisory Services team. We are seeking an experienced regulatory professional with deep expertise in medical device regulatory strategy, particularly with the U.S. FDA. This is a senior-level technical role for a regulatory expert who brings strategic insight, hands-on regulatory experience, and a proven ability to guide medical device companies through complex regulatory landscapes.
In the role of VP role, you will engage with potential new clients to understand their products and needs, design client support programs, lead client engagements, shape regulatory strategies for novel technologies, negotiate with regulators such as FDA, and provide expert guidance throughout the product lifecycle—from development through submission and post-market activities.
The role of Principal Consultant will involve the following;
General Responsibilities:
Own the overall client strategy.
Service as trusted advisor and strategist, helping clients solve their most critical business challenges.
Strong ability to synthesize all details, including client business needs, to produce a comprehensive strategy.
Ability to articulate complex concepts in a simple way which can be understood by cross-functional stakeholders.
Lead and direct client projects, ensuring strategic alignment and successful delivery.
Act as point of contact with regulatory authorities (e.g. FDA, Notified Body, TGA etc) as needed for the client.
Client Management:
Manage client accounts and maintain strategic, long-term relationships with
key client decision-makers.
Ability to interact with Senior level client personnel, Board of Directors, and Investors.
Ensure client’s best interests are represented at all times, balancing client needs with Avania’s capabilities.
Act as a bridge between the client’s executive team and the consulting team.
Handle complex or high-risk issues that may arise within the project, stepping in when there are significant problems or disputes to resolve.
Business Development:
Participate in new opportunity scoping calls, provide technical strategic input, craft proposals to support client needs, negotiate contracts.
Generate new business by identifying opportunities within existing accounts, proposing new services or solutions, and negotiating contracts.
Represent Avania in thought leadership activities, such as speaking at conferences or publishing articles, which can enhance Avania’s reputation and brand
This is an individual contributor role
The ideal candidate will have prior experience working at the FDA, combined with a strong understanding of regulatory requirements across multiple global markets, including the EU MDR, UK, Canada, and Australia. Experience working as a regulatory consultant or within a company developing a novel medical device is highly desirable.
We offer -
The opportunity to work in an innovative, fast-growing and rewarding industry
A dynamic and enthusiastic global team that fosters collaboration and the opportunity to work with experts across many specialties
Exchange of knowledge and ideas to help employees grow and advance their careers, backed with training and other development opportunities
Competitive compensation and benefits package (details shared during the interview process)
Some roles offer the opportunities for travel
Ask us about our hybrid and fully remote work opportunities
We look forward to receiving your application!
Avania takes pride in being an equal opportunity employer. We consider qualified applicants without regard to race, color, religion, gender, national origin, age, ****** orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.
#LI-DNI
💡 Quick Summary
Seeking a career-building opportunity? The Vice President, Regulatory and Advisory Services position is now open for candidates interested in the Work from home Jobs sector. This role in Toronto and East York offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Work from home Jobs is a plus.
