Top Benefits
About the role
We’re Hiring!
We are looking for a passionate and detail-driven Clinical Research Associate to join our mission in advancing neuro-regenerative therapies.
Epineuron is an early commercial stage medical device company on a singular mission to maximize human potential. We are focused on the development and commercialization of first-in-class therapeutic devices to aid in the surgical repair and treatment of peripheral nerves. Our lead product is a novel wearable that accelerates regeneration of injured nerves - it is designated an FDA Breakthrough Device and is Health Canada approved. We are growing a dynamic team to support ongoing and new clinical translation initiatives and are looking for talented individuals, like yourself, to join us!
This is an excellent opportunity for a recent graduate who:
✅ Is excited about clinical research and making a real-world impact
✅ Has a sharp analytical mind and loves digging into data
✅ Thrives in a friendly, open, and fun team culture that values unique perspectives
✅ Is open to 20-30% travel to clinical sites across Canada and the US
You’ll be reporting directly to the Clinical Research Manager, supporting the Clinical Application Specialists, and act as site monitor and liaison to the clinical trial sites.
Appointment
Contract Full-time (1.5 years), possibility for permanent full-time
Job Description
We are looking for a highly motivated and detail-oriented Clinical Research Associate (CRA) to join our growing Clinical Operations team. The CRA will play a critical role in the successful execution and oversight of our clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and all applicable regulatory requirements. This role requires a strong understanding of clinical trial processes, exceptional communication skills, and a passion for advancing innovative medical technologies that impact patient lives. You will report directly to the Clinical Research Manager, support the Clinical Applications Specialists, and act as site monitor and liaison to the clinical trial sites across Canada and the USA.
The CRA is responsible for coordinating study activities, ensuring compliance of the clinical trials, preparing/maintaining study documents, and engaging with the clinical trial sites.
The ideal candidate is an excellent team player, detail-oriented and organized, and ready to take on any challenge.
Responsibilities
● Conduct comprehensive site qualification, initiation, interim monitoring, and close-out visits in accordance with study protocols, Good Clinical Practice, and SOPs.
● Ensure the integrity of clinical data through source document verification, review of case report forms (CRFs), and resolution of data queries.
● Assess site performance, identify potential risks, and implement corrective and preventative actions as needed.
● Support and manage ethics board and regulatory submissions.
● Support audit and inspection readiness activities.
● Prepare site study training materials and conduct site training sessions.
● Organize and maintain clinical trial master files and investigational site files.
● Manage communication and correspondence with clinical trial sites and internal/external stakeholders.
● Manage and maintain study databases.
Qualifications
Required
● Bachelor’s degree in a life science and/or health-related discipline.
● Highly organized with meticulous attention to detail.
● Strong oral and written communication skills.
● Highly responsive to all communications.
● Excellent interpersonal skills to effectively engage with a diverse set of external stakeholders.
● Strong project management and time management skills.
● Critical thinker and problem solver, with the drive to work in a fast-paced environment.
● Proficient in MS Office (e.g., Word, Excel, PowerPoint, etc.).
● Valid driver’s license in good standing and passport with the ability to travel for business purposes.
Preferred
● 1-2 years of clinical trial coordination and management experience.
● Certificate and/or diploma in clinical research coordination.
● Graduate degree in life or health sciences (e.g., MSc or PhD).
● Direct involvement in preparation and submission of regulatory and/or ethics board applications.
● Direct experience with execution of clinical trials and engagement with various clinical site stakeholders (e.g., principal investigators, research coordinators, etc.).
● Experience in medical device studies in surgical specialties including plastics, orthopedics, and neurosurgery.
● In-depth knowledge of ISO 14155, Good Clinical Practice, and medical device regulatory requirements.
Why you’ll love working at Epineuron
● Be part of a groundbreaking company developing innovative solutions to address significant unmet medical needs in nerve recovery.
● Opportunity to work on an FDA Breakthrough Device designated technology.
● We have a friendly, open, and fun team culture that values unique perspectives.
● We enjoy discovering great foods locally and drink great coffee, fresh ground and brewed.
Added perks we offer
● A full benefit package including medical and dental for full-time employees
● An open, collaborative and inclusive work environment.
● Our head office includes a modern gym, volleyball court, basketball court, a calisthenics park.
● On-site parking and EV charging stations
● Excellent coffee, seriously.
Location & Hours
1875 Buckhorn Gate, Mississauga, ON, L4W 5P1
Full time (Monday to Friday at 8 hours per day or 40 hours per week).
Travel 20-30% of the time (Canada and USA).
Compensation c ommensurate with experience
Anticipated Start Date July 2025
Application Process
Please submit your resume/CV and cover letter through the link provided.
We can shape the future of nerve repair, together!
#Hiring #ClinicalResearch #medtech #nerveregeneration #RecentGradJobs #MedTechCareers #Epineuron
About Epineuron
Epineuron has combined cutting-edge advances in neuroscience, surgery, and biomedical engineering to create PeriPulse™ - a groundbreaking solution to deliver a novel, drug-free, bioelectronic therapy that supercharges the regeneration of damaged peripheral nerves.
Top Benefits
About the role
We’re Hiring!
We are looking for a passionate and detail-driven Clinical Research Associate to join our mission in advancing neuro-regenerative therapies.
Epineuron is an early commercial stage medical device company on a singular mission to maximize human potential. We are focused on the development and commercialization of first-in-class therapeutic devices to aid in the surgical repair and treatment of peripheral nerves. Our lead product is a novel wearable that accelerates regeneration of injured nerves - it is designated an FDA Breakthrough Device and is Health Canada approved. We are growing a dynamic team to support ongoing and new clinical translation initiatives and are looking for talented individuals, like yourself, to join us!
This is an excellent opportunity for a recent graduate who:
✅ Is excited about clinical research and making a real-world impact
✅ Has a sharp analytical mind and loves digging into data
✅ Thrives in a friendly, open, and fun team culture that values unique perspectives
✅ Is open to 20-30% travel to clinical sites across Canada and the US
You’ll be reporting directly to the Clinical Research Manager, supporting the Clinical Application Specialists, and act as site monitor and liaison to the clinical trial sites.
Appointment
Contract Full-time (1.5 years), possibility for permanent full-time
Job Description
We are looking for a highly motivated and detail-oriented Clinical Research Associate (CRA) to join our growing Clinical Operations team. The CRA will play a critical role in the successful execution and oversight of our clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and all applicable regulatory requirements. This role requires a strong understanding of clinical trial processes, exceptional communication skills, and a passion for advancing innovative medical technologies that impact patient lives. You will report directly to the Clinical Research Manager, support the Clinical Applications Specialists, and act as site monitor and liaison to the clinical trial sites across Canada and the USA.
The CRA is responsible for coordinating study activities, ensuring compliance of the clinical trials, preparing/maintaining study documents, and engaging with the clinical trial sites.
The ideal candidate is an excellent team player, detail-oriented and organized, and ready to take on any challenge.
Responsibilities
● Conduct comprehensive site qualification, initiation, interim monitoring, and close-out visits in accordance with study protocols, Good Clinical Practice, and SOPs.
● Ensure the integrity of clinical data through source document verification, review of case report forms (CRFs), and resolution of data queries.
● Assess site performance, identify potential risks, and implement corrective and preventative actions as needed.
● Support and manage ethics board and regulatory submissions.
● Support audit and inspection readiness activities.
● Prepare site study training materials and conduct site training sessions.
● Organize and maintain clinical trial master files and investigational site files.
● Manage communication and correspondence with clinical trial sites and internal/external stakeholders.
● Manage and maintain study databases.
Qualifications
Required
● Bachelor’s degree in a life science and/or health-related discipline.
● Highly organized with meticulous attention to detail.
● Strong oral and written communication skills.
● Highly responsive to all communications.
● Excellent interpersonal skills to effectively engage with a diverse set of external stakeholders.
● Strong project management and time management skills.
● Critical thinker and problem solver, with the drive to work in a fast-paced environment.
● Proficient in MS Office (e.g., Word, Excel, PowerPoint, etc.).
● Valid driver’s license in good standing and passport with the ability to travel for business purposes.
Preferred
● 1-2 years of clinical trial coordination and management experience.
● Certificate and/or diploma in clinical research coordination.
● Graduate degree in life or health sciences (e.g., MSc or PhD).
● Direct involvement in preparation and submission of regulatory and/or ethics board applications.
● Direct experience with execution of clinical trials and engagement with various clinical site stakeholders (e.g., principal investigators, research coordinators, etc.).
● Experience in medical device studies in surgical specialties including plastics, orthopedics, and neurosurgery.
● In-depth knowledge of ISO 14155, Good Clinical Practice, and medical device regulatory requirements.
Why you’ll love working at Epineuron
● Be part of a groundbreaking company developing innovative solutions to address significant unmet medical needs in nerve recovery.
● Opportunity to work on an FDA Breakthrough Device designated technology.
● We have a friendly, open, and fun team culture that values unique perspectives.
● We enjoy discovering great foods locally and drink great coffee, fresh ground and brewed.
Added perks we offer
● A full benefit package including medical and dental for full-time employees
● An open, collaborative and inclusive work environment.
● Our head office includes a modern gym, volleyball court, basketball court, a calisthenics park.
● On-site parking and EV charging stations
● Excellent coffee, seriously.
Location & Hours
1875 Buckhorn Gate, Mississauga, ON, L4W 5P1
Full time (Monday to Friday at 8 hours per day or 40 hours per week).
Travel 20-30% of the time (Canada and USA).
Compensation c ommensurate with experience
Anticipated Start Date July 2025
Application Process
Please submit your resume/CV and cover letter through the link provided.
We can shape the future of nerve repair, together!
#Hiring #ClinicalResearch #medtech #nerveregeneration #RecentGradJobs #MedTechCareers #Epineuron
About Epineuron
Epineuron has combined cutting-edge advances in neuroscience, surgery, and biomedical engineering to create PeriPulse™ - a groundbreaking solution to deliver a novel, drug-free, bioelectronic therapy that supercharges the regeneration of damaged peripheral nerves.