Biostatistician - Remote Canada

Emmes; Vancouver; Hybrid; CAD 70,000 - 90,000; Full time

Job summary

A global clinical research organization is seeking a Biostatistician to support clinical studies in Vancouver. You will collaborate on study designs, write statistical analysis plans, and conduct statistical analyses. A Master's degree in biostatistics or a related field is required, along with programming skills in SAS or R. Join a company that values integrity, excellence, and collaborative partnerships, offering a competitive benefits package including unlimited approved leave and professional development opportunities.

Benefits

Unlimited Approved Leave

Extended Healthcare Insurance

RRSP Contribution

Tuition Reimbursement

Maternity / Parental Leave Top Up

Wellness & Healthcare Spending Account

Qualifications

• Proficiency with statistical methods and applications in clinical research.
• Ability to manage multiple tasks effectively.
• Independence and teamwork capabilities.

Responsibilities

• Collaborate with clinical investigators to determine study design.
• Write statistical analysis plans and validate application programs.
• Generate study reports for internal and external monitoring.

Skills

Statistical methods

SAS programming

R programming

Teamwork

Communication

Education

MS in biostatistics or related field

Job description

Overview

Job Posting Title

CA Remote / Vancouver

TheEmmesCompany, LLC(“Emmes”) isa global, full-service Clinical Research Organization dedicated to excellence in supporting the advancement of public health and biopharmaceutical innovation. We believe in the power of truth, so much so that we named our companyEmmes, which means truth. Through decades of experience we have learned that collaborative relationships thrive and human health benefits when truth is our compass.

Our“Character Achieves Results”culture is driven by five key valuesthat guide our actions in the way we conduct research and distinguish us as an organization : Integrity, Agility, Passion for Excellence, Collaborative Partnerships and Intellectual Curiosity. Wearea trusted partner to clients who share our passion for improving public health in a world of ever-changing scientific research.

If you share our motivations and passion in research, come join us! You will be joining acollaborative culture that empowers everyEmmesemployee — from entry level through top executive — to contribute to our clients’ success by sharing ideas openly and honestly.

Primary Purpose

The Biostatistician (Masters) collaborates with clinical investigators to determine study design, contributes to protocol development, writes statistical analysis plans, performs statistical analysis, makes statistical inference and writes and presents reports summarizing findings including publications in peer-reviewed journals.

Responsibilities

• Collaborating with clinical investigators to determine study design;
• Writing sections of protocols that require statistical input;
• Reviewing protocols and case report forms to ensure that protocol objectives are met and standards are maintained;
• Generating treatment allocations in randomized clinical research studies and ensuring proper implementation;
• Leading the project team’s development of statistical analysis plans and programs to perform analyses and display study data;
• Performing statistical analyses; writing and validating application programs;
• Implementing data and safety monitoring reports to ensure participants’ safety;
• Developing metrics and generating quality control reports to optimize the performance of clinical sites and the coordinating center;
• Generating study reports to be distributed to internal and external monitoring committees and regulatory bodies;
• Participating in professional development activities both within and outside the company
• Other duties as assigned

Qualifications

• MS in biostatistics, statistics or related field.
• At least 2 years of related experience is expected but not required for the position.
• Demonstrated proficiency with statistical methods and applications in clinical research.
• Strong programming skills in SAS and / or R.
• Ability to manage multiple tasks.
• Ability to work independently, as well as in a team environment.
• Ability to effectively communicate technical concepts, both written and oral.

Emmes only requires all US new hires in the following job categories to be fully vaccinated before their first day of employment : (i) Clinical Research Associates (CRAs), (ii) Associate CRAs, and (iii) all CRA line managers. All new hires may also be required to comply with other COVID-19 health and safety protocols, such as masking or testing. Emmes complies with all applicable laws regarding reasonable accommodations or exemptions for religious, medical, or other legally protected reasons.

Why work at Emmes?

At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including :

• Unlimited Approved Leave
• Extended Healthcare Insurance
• RRSP Contribution
• Tuition Reimbursement / Professional Development
• Maternity / Parental Leave Top Up
• Wellness & Healthcare Spending Account