Clinical Research & Regulatory Affairs Intern

Embark on an exciting journey at PulseMedica! As an intern on the Clinical Research team, you’ll support the development of clinical research protocols, assist with documentation, and help coordinate efforts towards regulatory submissions for innovative medical devices. You'll contribute to impactful work that helps showcase the clinical benefits of PulseMedica’s groundbreaking technologies. This is an exciting opportunity to learn and grow within a dynamic, fast-paced medical device startup environment.

About Us

PulseMedica, recently certified as a Great Place to Work for the second consecutive year, is a fast-growing disruptive medical device startup company. We seamlessly integrate research, innovation, and production environments. We are determined to help those suffering from eye diseases and disabilities by offering novel treatment options using our state of the art technologies. Our platform combines real-time 3D eye imaging and high precision Femtosecond laser surgery. Our goal is to revolutionize ophthalmic treatments by providing people with exceptional outcomes and, ultimately, changing the world by preventing blindness and disability resulting from eye diseases.

The Opportunity

As a Clinical Research & Regulatory Affairs Intern, you’ll gain hands-on experience in the medical device field while supporting a range of pre-clinical, clinical, and regulatory activities. You will assist the clinical and regulatory teams with documentation, research, coordination, and communication with stakeholders. You’ll also be exposed to key aspects of regulatory strategy and preclinical and clinical trial design. This internship is ideal for students looking to pursue a career in clinical research, medical devices, or regulatory affairs.

Responsibilities:

• Assist with the preparation and organization of clinical and regulatory documents such as study protocols, reports, and ethics board submissions
• Support literature reviews and background research for regulatory and clinical planning
• Help maintain tracking tools and documentation related to regulatory submissions and clinical studies
• Participate in team meetings and take meeting notes and action items
• Assist with internal and external communications with clinical sites, consultants, and advisory board members
• Support data collection, analysis, and the preparation of presentation materials
• Help coordinate logistics for meetings, training sessions, or site visits
• Support general experimental and lab-based activities, which may include assisting with laboratory experiments using ex vivo animal specimens
• Contribute to organizing information for conference submissions, publications, and white papers
• Perform other administrative and research support duties as assigned

Qualifications:

• Currently enrolled in or recently graduated from a Bachelor's or Master’s program in a health sciences, life sciences, biomedical engineering, or a Regulatory Affairs Certificate or Diploma program
• Interest in clinical research, regulatory affairs, or medical devices, supported by relevant coursework or training
• Strong organizational and communication skills
• Ability to work independently and collaboratively in a team environment
• Detail-oriented and eager to learn
• Proficient in Microsoft Office and comfortable learning new tools
• Must be a Canadian citizen, permanent resident, or person to whom refugee protection has been conferred under the Immigration and Refugee Protection Act for the duration of the employment.
• Must have a valid Social Insurance Number at the start of employment and be legally entitled to work in Canada in accordance with relevant provincial or territorial legislation and regulations.

Anticipated Start Date: September 2, 2025 or as soon as a suitable candidate is available

Duration: Full-Time Permanent (40 hours per week)

Salary: $22 - $28/hour

Location: Edmonton (remote work may be considered)

What you can expect from PulseMedica:

• Free on-site gym (Jackson’s Gym)
• A role that contributes to helping change people’s lives by enhancing their vision
• A unique opportunity to build, grow, and be part of a team that is going to revolutionize a multi-billion dollar industry
• Growth Opportunities
• Monthly team events
• Working for a company that was recently Great Place to Work
  certified!
  

We believe that diverse teams perform better and that fostering an inclusive work environment is a key part of growing a successful team. We welcome people of diverse backgrounds, experiences, and perspectives to apply for this position.