- May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies.
- Provides expert consultation to projects across the company on statistical methodology.
- Solves problems of complex statistical scope.
- Provides technical review of proposed statistical design for research studies across company.
- Serves as the lead Biostatistician on one or more study projects.
- Participates in statistical process development and improvement across company.
- May present at statistical conferences.
- Provides sound strategic, scientific and statistical input to support client's research projects.
- Leads the project team's development of study analysis plans and statistical programs to perform analyses and display study data.
- Keeps abreast with current statistical and medical literature to ensure that sound methodologies are adopted.
- Fosters innovation in Biostatistics that will continuously enhance current statistical knowledge and practices.
- Ensures the scientific integrity of the research project and the accuracy of the reported results.
- Performs sample size calculation and provides leadership in the statistical design of research projects.
- Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained.
- Develops study assignment allocation schemas along with appropriate documentation.
- Leads the development of the methods and results sections of clinical study reports and scientific publications.
- Represents EMMES on behalf of clients at regulatory meetings.
- Provides expertise in methodological advances both internally and externally to improve statistical methodologies.
- Participate in the development and updating of Standard Operating Procedures.
- Other duties as assigned
- MS in biostatistics, statistics, or PhD in biostatistics, statistics, epidemiology or related field
- At least 4 years of related experience with MS or 1 year of related experience with PhD is expected but not required.
- Experience with methodological statistical research, including publication and/or presentation of work in statistical methods development.
- Demonstrated proficiency with statistical methods and applications in clinical research.
- Strong programming skills in SAS and/or R.
- Expertise in state-of-the-art data manipulation and statistical methodology.
- Excellent communication, interpersonal and organization skills.
- Ability to manage multiple tasks.
- Ability to work independently, as well as in a team environment.
- Ability to effectively communicate complex statistical concepts, both written and oral.
- Unlimited Approved Leave
- Extended Healthcare Insurance
- RRSP Contribution
- Tuition Reimbursement / Professional Development
- Maternity/Parental Leave Top Up
- Wellness & Healthcare Spending Account
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Senior Biostatistician - Vancouver, Canada - Emmes
Description
Overview
Senior Biostatistician
CA Remote
The Emmes Company, LLC ("Emmes") is a 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 company Emmes, 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 values that 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. We are a 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 a collaborative culture that empowers every Emmes employee — from entry level through top executive — to contribute to our clients' success by sharing ideas openly and honestly.
Primary Purpose
Leads collaborations with clinical investigators to determine study design, contributes to protocol development, authors statistical analysis plans, performs statistical analysis, makes statistical inference and writes and presents reports summarizing findings including publications in peer-reviewed journals. Manages statistical activities for a clinical study or platform of clinical studies.
Responsibilities
Qualifications
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:
