Consultant - Advisory Services

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 2 x Consultants - Advisory Services

Salary range $100,000 up to $120,000 + annual performance related bonus + benefits

About Avania

Avania Clinical is the world's only global CRO exclusively focused on medical technology, serving 90% of the top 50 MedTech companies across eight offices on three continents

Our Advisory Services division provides premium consulting across regulatory strategy, quality and compliance, market access and reimbursement, R&D engineering, and AI/SaMD guidance. We work with everyone from Series A startups bringing their first device to market to Fortune 500 MedTech leaders launching next-generation AI-enabled platforms

The Regulatory and Advisory Services team is responsible for the development of a wide range of deliverables for clients, including but not limited to:

• Strategic regulatory support from global jurisdictions
• Clinical strategy development
• Product development, design and engineering services
• Quality management strategy, establishment and execution

The Consultant role will participate in a variety of client project activities based on their specific background and experience, interests, and the contracted project work available.

General Responsibilities include:

• Perform project work with strategic input and minimal oversight. Holds either a broad, general consulting skill set or technical depth in a specific consulting skill set Project Management:
• Manage specific project workstreams and interact directly with clients to ensure work is completed on budget and to client expectations.

Client Management:

• Lead specific client interactions, with oversight of more senior team members. Build rapport with clients by developing high quality deliverables, consistently meeting project deadlines, and ensuring precise and timely communication.
• Prepare materials or reports that will be presented to the client, ensuring they are aligned with the Client’s objectives.
• Gather Client-specific data and information for senior project team members
• Attend Client meetings and provide support where necessary.

Business Development:

• Support new opportunity development by proofreading or providing initial drafts of new Statement of Work or Work Orders, as requested

Candidates who offer any combination of the skills, knowledge and experience listed below, are encouraged to apply for the role of Consultant.

What we're looking for.

• The Consultant roles requires competencies such as Design History File work, nonclinical testing strategy, and FDA research strategy
• Degree in health care, science, technology or industry-related discipline, or equivalent industry experience
• Knowledge of regulations and guidelines on medical technology. Industry context in MedTech, medical devices, diagnostics, or adjacent regulated industries. You've heard of 510(k) and MDR, even if you can't recite the regs
• Ability to provide client consulting in a broad range of topics, based on knowledge of regulations and guidelines on MedTech OR ability to provide detailed, deeply technical consulting in a specific technical area.
• Proficient in the use of computer and software systems (Microsoft Word, Excel, PowerPoint, email).
• Fluent in English, spoken and written.
• Ability to travel domestically and internationally

#LI-DNI