> job detail
C
🧪Data Scientist
Associate Director Biostatistician Consultant (24 months contract)
ClinChoice · Canada
// classified as
Data Scientist (Modeling, experiments, research.)
posted
2d ago
location
Canada
languages
c, r, sas
tools
—
> stack
crsas
> education
msphd
> description
<p></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….</span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is searching for an <strong>Associate Director</strong> <strong>Biostatistician Consultant </strong>to join one of our clients.</span><br><br></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. </span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong><br><span style="text-decoration: underline;">Job Duties</span></strong></span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">This position will require minimal supervision from senior department staff and able to represent the Biostatistics function for complex studies or at project level. The position is responsible for working with study team members to independently contribute to design of early/late-stage protocols across multiple therapeutic areas, help draft protocols or amendments, develop and write statistical analysis plans, and perform statistical analyses for interim and final reports to be submitted to regulatory agencies.</span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">The position will also support submission activities, including design, analysis and reporting of integrated summaries for safety and efficacy.</span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Attendance and statistical contributions at study team meetings or project level meetings (if needed) are expected.</span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Within the BDM Department, leadership skills are needed to contribute to the organization and scheduling of study deliverables in collaboration with Statistical Programmers and Data Managers. </span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"> </span></p>
<p style="line-height: 1.2;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><strong><span style="text-decoration: underline;">Qualification and Required Skills</span> </strong></span></p>
<ul>
<li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">MS or PhD in Statistics or Biostatistics</span></li>
<li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">PhD + 6 years (or MS + 11 years) clinical trial experience in either a biotechnology or pharmaceutical company</span></li>
<li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Hands-on Phase I/II/III clinical trial experience and proficient in SAS programming. Excellence in R programming desirable.</span></li>
<li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Excellent oral and written communication skills.</span></li>
<li style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: 12pt;">Although not required, previous experience with regulatory submissions in the US, Europe, Japan, and Rest of the World, is desirable.</span></li>
</ul>
<p></p>
<p><strong>Open Date: 5/15/2026</strong></p>
<p><strong>Close Date: 6/3/2026</strong></p>
<p> </p>
<p><em>ClinChoice Canada Inc. is proud to be an equal opportunity employer, valuing and respecting diversity. We are committed to inclusive, barrier-free recruitment and selection processes. We will accommodate the needs of qualified applicants under the Human Rights Code and the Accessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 (647)724-5709 x 301. </em></p>
<p><em>We thank all applicants for their interest; however, only those being considered for an interview will be contacted. In accordance with Federal Personal Information Protection and Electronic Documents Act ("PIPEDA") , personal information is collected under the authority of the Act and will only be used for candidate selection.</em></p><div class="content-pay-transparency"><div class="pay-input"><div class="description"><p><span class="ui-provider a b c d e f g h i j k l m n o p q r s t u v w x y z ab ac ae af ag ah ai aj ak">The base salary pay range represents the anticipated low and high range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. </span></p></div><div class="title">Canada Pay Range</div><div class="pay-range"><span>$120</span><span class="divider">—</span><span>$165 CAD</span></div></div></div>