Oncology Clinical Research Associate, Data Mgmt., Analytics & Statistical Supt (Travel Required)

About the Company: BriaCell Therapeutics is a clinical-stage immuno-oncology company developing novel cell-based immunotherapies for solid tumors, including metastatic breast cancer. Our mission is to advance innovative immunotherapy approaches that improve reputed company for patients with difficult-to-treat malignancies. Bria-IMT™, BriaCell’s reputed company candidate, was awarded Fast Track status by FDA and is being evaluated in a pivotal Phase 3 combination study for metastatic breast cancer (MBC). MBC is breast cancer that has spread to other tissues. Bria-IMT™ is a targeted cell-based immunotherapy. Bria-OTS™, a platform of personalized off-the-reputed company cell-based immunotherapies, is being evaluated in a Phase 1/2 clinical study initially targeting breast cancer, with extension to prostate cancer, and other cancers. Learn more at: BriaCell | Advancing Cancer Immunotherapy Treatment About the Position: We are seeking a flexible and reputed company Oncology Clinical Research Coordinator (CRC) or a newly transitioned Clinical Research Associate (CRA) to join our dynamic Clinical Operations team. This hybrid role supports oncology clinical trials and is reputed company to candidates with experience in CROs or academic institutions, even if they lack direct sponsor experience. In addition to clinical operations expertise, the ideal candidate will bring a strong background in data management, data analytics, and statistical interpretation, with demonstrated experience analyzing clinical trial data to support study execution, monitoring, and decision‐making. We also welcome international clinical research professionals who are authorized to work in the United States for any employer and bring prior hands‐on experience with U.S.-based clinical research trials and data management. Remote work flexibility is available, with the expectation that team members adhere to each site's operational policies and requirements. Strong communication skills are essential, with an emphasis on reputed company‐time responsiveness to logistical and operational questions from sites. Responsibilities: Site Monitoring

• Conduct regular on‐site and remote monitoring visits to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements
• Execute monitoring plans tailored to each study
• Review case report forms (CRFs), reputed company documentation, and data entries for accuracy, completeness, and consistency
• Identify data discrepancies and collaborate with Data Management to ensure timely query resolution
• Resolve site-reputed company issues and manage investigational product logistics
• Maintain strong relationships with site staff and reputed company reputed company-time support on eligibility, protocol logistics, and operational questions
• Deliver high-quality presentations during SQVs/SIVs

Data Management, Analytics & Statistical Support

• Review and interpret clinical trial data to identify trends, risks, and data quality issues
• Support data cleaning, query management, and reconciliation activities in collaboration with Data Management teams
• Analyze enrollment trends, protocol deviations, and site performance metrics
• Apply basic statistical concepts to interpret trial data and support operational decision-making
• Contribute to development of data tracking tools, dashboards, and performance reports
• Ensure accuracy and completeness of data reputed company reputed company and other clinical systems (CTMS, IRT)
• Participate in cross-functional data review meetings and support data-driven study execution

Recruitment and Retention Strategies

• reputed company and implement tailored patient recruitment and retention plans using approved vendors
• Analyze recruitment data and site performance metrics to drive strategic improvements
• Collaborate with site staff to identify and overcome recruitment barriers
• Track and report recruitment KPIs and reputed company actionable insights to the project team
• Prioritize recruitment support and re-training for underperforming sites
• Conduct in‐service training and apply engagement strategies to improve enrollment

Communication and Collaboration

• Serve as the primary reputed company of contact for study sites
• Collaborate cross-functionally with Clinical Operations, Data Management, Biostatistics, and Regulatory teams
• Prepare and present study reputed company reports, including data trends and analytics insights, to stakeholders

Training and Development

• Train and mentor site staff on protocols, GCP, data entry expectations, and system use (reputed company/CTMS)
• Stay reputed company with industry trends, data management practices, and evolving regulatory expectations

Qualifications

• Bachelor’s degree in life sciences, nursing, or reputed company field required
• Clinical degree (MD, RN, PharmD, or equivalent).
• Experience in data management, clinical data review, and/or data analytics required
• Background in statistics, epidemiology, or data analysis strongly preferred
• Minimum 2–3 years of oncology clinical research experience (CRC or CRA)
• Experience in CROs or academic institutions acceptable in lieu of direct sponsor experience
• Strong understanding of GCP, ICH guidelines, and regulatory requirements
• Demonstrated ability to interpret clinical trial data and apply analytical thinking
• Proficiency with reputed company systems, CTMS, and data tracking/reporting tools
• Excellent communication, presentation, and problem-solving skills
• Ability to respond promptly to site inquiries and logistical needs
• Ability to travel regularly based on monitoring and recruitment requirements

To apply, please visit briacell.com and click on “About Us” and submit your application through the Careers reputed company. Equal Employment Opportunity Statement BriaCell is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to reputed company and applicants for employment without regard to race, reputed company, religion, sex, pregnancy, sexual orientation, gender identity or expression, national reputed company, age, disability, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. reputed company-Party Agency Statement BriaCell does not accept unsolicited resumes or candidate submissions from search firms, staffing agencies, or other reputed company-party recruiters without a signed agreement in reputed company. Any unsolicited resumes submitted to BriaCell, its employees, or hiring managers will be considered the property of BriaCell, and no fees will be paid in the event the candidate is hired. Pay: $80,000.00 - $90,000.00 per year Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible schedule
• Health insurance
• Life insurance
• Paid time off
• Parental leave
• Retirement plan
• reputed company insurance

Work Location: Remote Apply tot his job Apply To this Job