Neuromuscular Funding and Employment Opportunities
Selected presenters will have the opportunity to showcase their work to a national audience of neuromuscular specialists, receive expert feedback, expand their professional network, and receive complimentary conference registration and a $250 honorarium. Read the full invite and participate on conference website wcnmc.ca
Application Deadline: September 4, 2026 (midnight ET)
The Cure SMA Basic Research RFP supports innovative research aimed at advancing the understanding of spinal muscular atrophy (SMA) at the molecular, cellular, and biochemical levels, with a focus on uncovering disease mechanisms, identifying therapeutic targets, and developing tools to accelerate treatment strategies. Open to researchers worldwide, including principal investigators and postdoctoral fellows, the program provides up to $75,000 per year for up to two years, with proposals evaluated based on scientific merit and alignment with Cure SMA’s research priorities.
The Department of Pediatrics at CHEO, University of Ottawa is recruiting a full-time pediatric neurologist within the Division of Neurology. Priority will be given to candidates with:
• Certification with the Royal College of Physicians of Surgeons (Neurology) although equivalent training in other countries/jurisdictions will be considered;
• Subspecialty training and expertise in Pediatric Epilepsy;
• Certification in EEG with the Canadian Society of Clinical Neurophysiologists (CSCN) and/or the American Board of Electrodiagnostic Medicine.
Application Deadline: 20 July 2026
The NeuroMuscular Centre at The Ottawa Hospital is continuing to expand, and is recruiting Neuromuscular Neurologist to join their growing program as a Clinician-Scientist (Tier 2 Canada Research Chair with salary support)
The Rare Disease Foundation, in partnership with REACH Trauma Response Consulting and BC Children’s Hospital Foundation, is offering bursaries to help rare disease families across Canada access online counselling with specially trained mental health providers at a significantly reduced cost. While the program primarily supports youth with a rare disease, bursaries may also be available for parents, guardians, caregivers, and siblings, recognizing that family wellbeing is deeply interconnected. Applications are accepted on a rolling basis through the submission form, and decisions are typically provided within two (2) weeks.
Registration is now ongoing for the NMD4C Neuromuscular Talent Pool. The Talent Pool is intended to be used as a viewing and discovery resource by laboratories, institutions, and research teams. If you would like to be included in the Neuromuscular Talent Pool, you are invited to register by completing the short registration form below and uploading your CV along with a brief personal statement. The personal statement should outline your experience, your interest in neuromuscular research, and the type of position you are seeking next.
Deadline for submissions: 1 October 2026.
The award consists of a prize of €10,000 and is intended to start a new project or to further develop or implement an existing initiative that contributes to improving the care and daily lives of people with Duchenne. The winner will be selected by an expert jury chaired by Dr. Imelda de Groot.
Projects eligible for the award are practical, innovative, and directly applicable. This may involve starting a new project or supporting or further developing an existing initiative.
Proposals Due: September 4, 2026.
The Myotonic Dystrophy Foundation (MDF) is soliciting scientific proposals for two types of Early Career Scholar awards,
1. an “Early Career Scholar- Basic/Translational Science” award and
2. an “Early Career Scholar- Clinical Research” award.
Eligible research includes projects focused on improving treatment, care, and support for DM patients and their families, as well as fundamental basic science investigations. Applicants must demonstrate a clear plan for contributing to the DM field.
Proposals Due: September 4, 2026.
The Myotonic Dystrophy Foundation (MDF) is now accepting applications for its 2027 Doctoral and Postdoctoral Research Fellowships.
This fellowship program supports research projects focused on basic, translational, and clinical aspects of myotonic dystrophy, as well as projects that aim to improve the care and quality of life of people living with DM. Fellowships are for projects conducted under the supervision of qualified sponsors in academic institutions or research institutes.
Did you know RareKids-CAN offers a range of subsidized services for investigator-initiated (academic-led) pediatric rare disease clinical trials?
See more career opportunities:
- the Canadian Neurological Sciences Federation (CNSF) Neuro Career Webpage
- the World Muscle Society (WMS) Job Postings