Top 1817 Statistical Data Associate Jobs

Oncology Clinical Research Associate, Data Mgmt., Analytics & Statistical Supt (Travel Required)
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- Medicine
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Everest Clinical Research —Bridgewater, NJ
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Principal Associate, Data Scientist - US Card (Generative AI Systems)
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Research Associate 3, Miami Neuroscience Research, FT,8:00am - 4:30pm
Baptist Health South Florida —Miami, FL
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Oncology Clinical Research Associate, Data Mgmt., Analytics & Statistical Supt (Travel Required)

BriaCell Therapeutics, Inc.
Remote

Quick Apply

Job Details

Full-time
$80,000 - $90,000 a year

Benefits

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

Qualifications

Statistics
Operational analysis
Teamwork
Statistics
Collaboration
Bachelor's degree
Oncology research
Oncology

Full Job Description

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 outcomes for patients with difficult-to-treat malignancies.

Bria-IMT™, BriaCell’s lead 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-shelf 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 experienced 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 open 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 real‐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), source documentation, and data entries for accuracy, completeness, and consistency
Identify data discrepancies and collaborate with Data Management to ensure timely query resolution
Resolve site-related issues and manage investigational product logistics
Maintain strong relationships with site staff and provide real-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 within EDC and other clinical systems (CTMS, IRT)
Participate in cross-functional data review meetings and support data-driven study execution

Recruitment and Retention Strategies

Develop 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 provide 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 point of contact for study sites
Collaborate cross-functionally with Clinical Operations, Data Management, Biostatistics, and Regulatory teams
Prepare and present study progress 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 (EDC/CTMS)
Stay current with industry trends, data management practices, and evolving regulatory expectations

Qualifications

Bachelor’s degree in life sciences, nursing, or related 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 EDC 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 section.

Equal Employment Opportunity Statement

BriaCell is an Equal Opportunity Employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Third-Party Agency Statement

BriaCell does not accept unsolicited resumes or candidate submissions from search firms, staffing agencies, or other third-party recruiters without a signed agreement in place. 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
Vision insurance

Work Location: Remote

Quick Apply

Refine Your Search

Statistical Data Associate jobs

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

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