Posted 3 months ago
Regulatory & Market Access Intern
@ Avania
Canada
Overview
Avania is hiring a Regulatory & Market Access Intern for a six-month placement on its Advisory team. The intern supports medical device consulting projects, client deliverables and marketing initiatives alongside senior consultants. The posting requires current enrolment in a Northeastern University Master of Science in Regulatory Affairs, is open to Boston or Toronto campuses, and states that US work authorization is required with no visa sponsorship.
Responsibilities:
- Research medical device companies and consulting opportunities
- Support CRM data entry, client tracking and outreach
- Contribute to regulatory and quality-focused white papers and marketing materials
- Assist consultants with client work and report preparation
- Help maintain templates and knowledge management tools
Requirements summary:
- Current Northeastern University Master of Science in Regulatory Affairs student
- Strong research, writing and analytical skills
- Interest in ISO 13485, FDA QMSR and EU MDR/IVDR
- Proficient in Microsoft Office and online collaboration tools
- Local to Boston or Toronto campus
Tools & skills
Source and dates
Source type not verified · hirebridge
- Employer posting date
- 2026-08-17
- First seen by our source
- 2026-10-15
- Source record updated
- 2026-10-15
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Entry level |
| Department | Business development |
| Work setting | Office |
| Position | Mostly sitting |
| Physical demands | physical low · computer high |
| Languages | English |
| Education | Master’s degree (required) |
| Fields of study | Regulatory Affairs |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Avania
Saved company profile
Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.
The Only Global CRO Built for MedTech
Full company description
Avania is the only global CRO built for MedTech — integrating regulatory strategy, clinical development, and market access and reimbursement to take innovations from concept to commercialization with confidence. Avania was purpose-designed to serve medical technology innovators, combining regulatory, clinical, engineering, and market access expertise to guide products across the full lifecycle. We bring deep experience across a wide range of therapeutic areas, with particular strength in cardiovascular, neurovascular, and orthopedics: three of MedTech’s most complex and high-growth fields. Avania combines international reach with deep local expertise. Our regional teams understand the regulatory, cultural, and operational nuances that accelerate approvals and improve site engagement worldwide. Partner with Avania and experience the difference of a MedTech-only CRO: trusted expertise, collaborative engagement, and proven results.
- LinkedIn followers
- 22,109
- People associated on LinkedIn
- 372
- Reported office locations
- 100 Crowley, Suite 216, Marlborough, MA 01752, US
- Prof. Bronkhorstlaan 10, bld. 54, Bilthoven, MB 3723, NL
- 101 Federal St, Boston, Massachusetts 02110, US
- 3031 Tisch Way, San Jose, California 95128, US
- 250 Carlaw Ave, Toronto, Ontario M4M 3L1, CA
- Carrer de Sant Antoni Maria Claret, 167, Barcelona, Catalonia 08025, ES
- Friedrich-Ebert Anlage 49, Messeturm, 9th floor, Frankfurt, Hesse 60308, DE
- 71 Gipps St, Collingwood, Victoria 3066, AU
- 13/76 Reserve Rd, Artarmon, New South Wales 2064, AU
- Business categories
- Health Care
- Medical Device
- Clinical Trials
- Life Science
- Other recorded names
- Avania
- Specialties
- Medical Device Clinical Trials
- Regulatory Strategy
- Clinical Development
- Market Access and Reimbursement
- MedTech CRO Services
- Cardiovascular Devices
- Neurovascular Interventions
- Orthopedic Devices
- Musculoskeletal & Orthopedics
- Aesthetics & Dermatology
- Medical Device Regulatory Affairs
- Medical Urology
- Endocrinology
- Global Clinical Operations
- Med-Tech Focused CRO
- Global Market Access
- European Regulatory Affairs
- Multi-Regional Trials
- International Clinical Trials
- Integrated Regulatory-Clinical-Market Access
- Medical Device Commercialization
- Regional Regulatory Expertise
- FDA Guidance
- IVD/Diagnostic Studies
- Early Feasibility/First in Human Studies
- and Post-Market Surveillance
- Profile identifies a recruitment agency
- No
- Reported total investment
- 0
Currency and observation date were not supplied; this is not a current valuation or a funding round.
Avania is the only global CRO built for MedTech — integrating regulatory strategy, clinical development, and market access and reimbursement to take innovations from concept to commercialization with confidence. Avania was purpose-designed to serve medical technology innovators, combining regulatory, clinical, engineering, and market access expertise to guide products across the full lifecycle. We bring deep…
| Field | Value |
|---|---|
| Industry | Medical Equipment Manufacturing |
| Company size | 201-500 employees |
| Headquarters | Marlborough, MA |
| Organization type | Privately Held |
| Specialties | Medical Device Clinical TrialsRegulatory StrategyClinical DevelopmentMarket Access and ReimbursementMedTech CRO ServicesCardiovascular DevicesNeurovascular InterventionsOrthopedic DevicesMusculoskeletal & OrthopedicsAesthetics & Dermatology |
| Open jobs on Jobsy | 2 |
| View page |
Avania are Hiring – Regulatory & Market Access Intern
We are seeking, Medical Device Regulatory Affairs & Quality Intern to join the Advisory team for a six-month placement. The roles offer hands-on experience supporting medical device consulting projects, client deliverables, and strategic marketing initiatives. You will work directly with senior consultants to gain practical insight into medical device regulation, quality systems, and the business of consulting.
Key Responsibilities
- Lead Generation & Market Research
- Research emerging medical device companies and consulting opportunities.
- Support CRM data entry, client tracking, and outreach efforts.
- Content Development
- Contribute to creation of medical device regulatory and quality-focused white papers, blogs, and marketing materials.
- Conduct medical device literature and regulatory research to support technical writing.
- Quality & Regulatory Support
- Assist consultants on client work including:
- Support data organization and report preparation for client deliverables.
- Internal Process Support
- Help maintain templates and knowledge management tools.
Qualifications
- Current Northeastern University Master of Science in Regulatory Affairs students with interest in medical devices.
- Strong research, writing, and analytical skills.
- Interest in medical device regulation, ISO 13485, FDA QSR/QMSR, and EU MDR/IVDR.
- Proficient in Microsoft Office and collaborative online tools (SharePoint, Teams, or similar).
- Detail-oriented, self-motivated, and eager to learn in a fast-paced consulting environment.
- Local to either Boston or Toronto campuses
What You’ll Gain
- Exposure to real-world regulatory and quality projects in the medical device industry.
- Experience collaborating with senior consultants and clients across global markets.
- Skill-building in regulatory strategy, QMS development, and technical writing.
- Opportunity to contribute to visible marketing and thought leadership initiatives.
Applicants must be legally authorized to work in the United States at the time of hire. This internship is intended to serve as a pathway to full-time employment. Candidates must have authorization to work in the United States that does not require current or future employer-sponsored visa sponsorship, as sponsorship is not available for this internship or subsequent full-time employment.
We look forward to receiving your application!
Avania - MedTech's trusted Champion#LI-DNI
Qualifications
- Current Northeastern University Master of Science in Regulatory Affairs students with interest in medical devices.
- Strong research, writing, and analytical skills.
- Interest in medical device regulation, ISO 13485, FDA QSR/QMSR, and EU MDR/IVDR.
- Proficient in Microsoft Office and collaborative online tools (SharePoint, Teams, or similar).
- Detail-oriented, self-motivated, and eager to learn in a fast-paced consulting environment.
- Local to either Boston or Toronto campuses
What You’ll Gain
- Exposure to real-world regulatory and quality projects in the medical device industry.
- Experience collaborating with senior consultants and clients across global markets.
- Skill-building in regulatory strategy, QMS development, and technical writing.
- Opportunity to contribute to visible marketing and thought leadership initiatives.
Applicants must be legally authorized to work in the United States at the time of hire. This internship is intended to serve as a pathway to full-time employment. Candidates must have authorization to work in the United States that does not require current or future employer-sponsored visa sponsorship, as sponsorship is not available for this internship or subsequent full-time employment.
We look forward to receiving your application!
Avania - MedTech's trusted Champion#LI-DNI
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