Research Associate

Benefits

Qualifications

• •The ideal candidate is detail-oriented, highly organized, and comfortable working across disciplines, with a minimum of two years of relevant industry experience in biomedical or clinical research or drug development and demonstrated success working in a remote-first setting
• •Legally authorized to work in the United States; no visa sponsorship available
• •Master’s degree in a life sciences discipline (e.g., pharmacology, biology, neuroscience, or related field)
• •Minimum of 2 years of relevant industry experience supporting clinical trials or nonclinical studies in an industry setting
• •Strong scientific writing and communication skills
• •Experience conducting and summarizing scientific literature reviews
• •Exceptional attention to detail and organizational skills
• •Working knowledge of biostatistics and statistical software (e.g., SPSS, GraphPad Prism), with experience supporting data analysis, figure/table generation, and interpretation of nonclinical and/or clinical research data
• •Demonstrated ability to work effectively in a remote-first environment, including managing priorities independently, communicating clearly across time zones, and collaborating with cross-functional teams using digital tools
• •Note: this position is currently remote; however, future business needs may require occasional or regular on-site presence
• •Ability to travel within North America up to quarterly for meetings, site visits, or conferences
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Responsibilities

• •This role will work closely with internal scientific and regulatory leadership, as well as external collaborators, to support study design and execution, regulatory submissions, and the preparation of scientific and regulatory documentation across multiple stages of development
• •Clinical & Nonclinical Research Support
• •Support the planning, tracking, and execution of clinical and nonclinical studies, including investigator-initiated and Sponsored trials, qualitative studies and early-phase development programs
• •Assist in the authoring and review of study documentation, including protocols, ICFs, study reports, and scientific publications
• •Coordinate timelines, deliverables, and communications with CROs, academic collaborators, consultants, and SMEs
• •Support engagement with patient advocacy groups to incorporate patient perspectives into study design, endpoint selection, and communication materials
• •Regulatory & Compliance Support
• •Assist in the preparation, compilation, and maintenance of regulatory submissions (e.g., IND/CTA submissions, and IRB/REB submissions), ensuring that documentation aligns with applicable regulatory guidance (e.g., FDA, Health Canada, ICH)
• •Support document compliance activities
• •Scientific Writing & Literature Review
• •Conduct systematic literature reviews to support nonclinical safety, pharmacology, and clinical rationale
• •Summarize and synthesize emerging scientific data into internal reports, regulatory documents, and presentation materials
• •Assist with manuscript preparation, figure/table development, and data summaries as needed
• •General Research & Project Management
• •Maintain organized study files, trackers, and project documentation
• •Support internal data review meetings and preparation of materials for leadership or external stakeholders
• •Assist with ad hoc research, data analysis support, and cross-functional projects as needed
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