Job Description

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We are seeking a highly motivated and detail-oriented Clinical Research Intern to join our team. This internship provides an excellent opportunity to work in a fast-paced and dynamic start-up environment and gain hands-on experience with clinical trial operations and medical device research & development. The intern will be supervised by the Associate Clinical Research Manager and will contribute to critical aspects of clinical trial coordination, documentation, data collection and management.

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Responsibilities

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• Assist in preparing for and conducting clinical trial monitoring visits.

• Ensure accurate and complete data collection and data entry for clinical and technical activities.

• Assist in preparing and maintaining essential study documents, including the clinical trial master files.

• Support the coordination of study activities and document preparation according to Good Clinical Practices (GCP) and applicable standards.

• Assist in device usability analysis.

Qualifications

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• Currently enrolled in a relevant Life Sciences, Health Sciences, Biomedical Engineering, or related program.

• Strong organizational skills and exceptional attention to detail.

• Clear and professional written and verbal communication skills, including the ability to explain ideas, document findings, and ask clarifying questions when needed.

• Proficient in Microsoft Office Suite, with strong Excel and Access skills for data entry and basic analysis.

• Ability to handle confidential and sensitive information (e.g., patient data, clinical trial records) in accordance with privacy regulations and company policies.

• Eagerness to learn about clinical trial management, medical device technology, and regulatory compliance.

• Able to apply critical thinking when reviewing data, documentation, and technical procedures, and to ask questions when something doesn’t look right.

• Valid driver’s license and access to a personal vehicle, with the ability to travel locally in Southern Ontario (up to 40%).

 

Nice-to-Have Skills

• Experience in a hospital or clinical environment.

• Previous exposure to clinical research.

• Familiarity with the biophysics of nerve stimulation and nerve recording.

• Knowledge of peripheral nerve anatomy and physiology.

• Understanding of Design Control and general medical device standards (ISO 13485, IEC 60601-1).

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Term: 4 or 8 months (start date May 1, 2026)
Schedule: Full-time, Monday to Friday, 40 hours per week (8 hours per day).  Hybrid work Arrangement. Our head office is in
Mississauga near Dixie & Eglinton.

• Local travel within Southern Ontario, up to 40% of the time.

• Occasional evening and/or weekend work may be required depending on surgical case schedules.

 

Hiring Process:

1. Application Deadline: Interested candidates should submit their cover letter, resume and most recent transcripts by 5:00 PM on January 23th, 2026.

2. First-Round Interview (Video Call): Applications will be reviewed on a rolling basis. Selected candidates will be invited to a 15–20 minute video interview to discuss their background and interest in the position.

3. On-Site Interview: Candidates who advance beyond the first round will be invited to an onsite interview on a rolling basis.

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Epineuron is an equal opportunity employer. We are committed to providing a diverse and inclusive work environment, while providing ongoing education for all employees. Qualified applicants will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

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Please inform us if you require any accommodations during the recruitment process. While we thank all applicants, only those being considered for an interview will be contacted.

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​Please submit a resume/CV as a PDF.