Clinical Research Assistant/statistician

7 days ago

Hamilton, Canada Centre for Surgical Invention & Innovation (CSii) Full time

**Position Summary**:
The Clinical Research Assistant/Statistician plays a key role in supporting clinical research activities conducted by CMAS/CSii and affiliated Principal Investigators. Under the supervision of the Senior Research Coordinator, the role combines statistical expertise to facilitate the successful execution, analysis and dissemination of clinical research studies and administrative coordination.

**Statistical Analysis & Reporting**
- Identify appropriate statistical models and tools for various data sets.
- Generate statistical summaries, tables, visualizations, and interpretive reports for both internal and external stakeholders.
- Conduct data audits and quality checks to ensure accuracy and integrity.

**Key Responsibilities:Research Coordination & Support**
- Assist in planning, organizing, and coordinating clinical research projects to ensure adherence to timelines and regulatory standards.
- Collaborate with remote project sites and personnel to ensure consistent implementation of study protocols.
- Maintain detailed, organized records of study activities, data, and communications.
- Prepare study documentation, including protocols, case report forms (CRFs), patient information sheets, and consent forms.
- Contribute to regulatory submissions (e.g., REB, Health Canada).

**Knowledge Dissemination**
- Assist in preparing manuscripts, abstracts, grant proposals, presentations, and scientific reports.
- Perform literature reviews and critical appraisals of published research to inform study design and interpretation.
- Develop and present training sessions or data presentations to project personnel and stakeholders.

**Compliance & Ethics**
- Ensure that all research procedures follow Good Clinical Practice (GCP), ethical guidelines, and institutional protocols.
- Safeguard the confidentiality of participant data and maintain compliance with privacy regulations.

**Qualifications**:
**Minimum**:

- Bachelor’s degree in Statistics, Biostatistics, Epidemiology, Public Health, Health Sciences, or a related field.
- Minimum 2 years of relevant experience in a clinical research or healthcare research environment.

**Preferred**:

- Proficiency with statistical software (e.g., SPSS, R, SAS, STATA).
- Knowledge of clinical trial processes, ethical standards, and regulatory requirements.
- Strong analytical, organizational, and communication skills.
- Experience with preparing research publications and grant submissions.

**Key Competencies**:

- Attention to detail and data integrity
- Critical thinking and problem-solving
- Collaborative team player
- Strong written and verbal communication
- Ability to manage multiple tasks and prioritize deadlines

Pay: $57,000.00-$58,300.00 per year

**Benefits**:

- Casual dress
- Dental care
- Disability insurance
- Extended health care
- Life insurance
- Paid time off
- Vision care

Flexible language requirement:

- French not required

Schedule:

- Monday to Friday

Ability to commute/relocate:

- Hamilton, ON L8N 1Y3: reliably commute or plan to relocate before starting work (required)

**Education**:

- Bachelor's Degree (preferred)

**Experience**:

- Statistical analysis: 2 years (required)

Work Location: In person

Application deadline: 2025-06-22
Expected start date: 2025-08-11

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