882# Principal Statistical Programmer Consultant- Hematology (Remote) New

ClinChoice Inc.; Canada; Remote; CAD 90,000 - 130,000; Full time

Job summary

A leading global CRO is seeking a Principal Statistical Programmer Consultant to join their Hematology team. This remote role involves leading programming activities for clinical studies, requiring strong technical skills and the ability to work independently. Candidates should have significant experience in clinical programming, particularly in Oncology/Hematology, and a solid understanding of regulatory requirements.

Qualifications

• 6+ years of clinical programming experience for Bachelor's degree holders.
• 8+ years of clinical programming experience for Master's degree holders.
• Experience in Oncology/Hematology TA and knowledge of ICH and Good Clinical Practices.

Responsibilities

• Lead and support programming activities for clinical studies.
• Develop Tables, Figures, Listings (TFLs) from SAS programs.
• Ensure compliance with standards and contribute to best practices.

Skills

Clinical programming

SAS programming

Communication skills

Coordination skills

Education

Bachelor’s degree in computer science, statistics, or related field

Master’s degree in CS, statistics or related disciplines

Job description

882# Principal Statistical Programmer Consultant- Hematology (Remote)

Canada

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….

ClinChoice is searching for aLead/Principal Programmer Consultantto join one of our clients in Hematology TA Team.

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.

Main Job Tasks and Responsibilities:

The Principal Statistical Programmer consultant will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report and regulatory submission.This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks.

Key Responsibilities:

• Develop Tables, Figures, Listings (TFLs) deliverables from existing SAS programs for Clinical Study Report (CSR) if similar TFLs exist and from scratch for new outputs.
• Capacity for independent programming and review of reports and outputs.
• Customize outputs and graphics according to delivery specifications of target audience on the direction of biostatisticians.
• Responsible for supporting the Programming deliveries of a clinical study or project.
• Programs independently with high efficiency and quality.
• Contribute to the development of best practices to improve quality, efficiency, and effectiveness within the function.
• Ensures compliance with standards and automation usage.
• Plans and support team activities and tasks.
• Communicates and escalates risks within the assigned studies and/or projects.

Education and Experience:

• Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 6 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 8 yrs. of clinical programming (CDISC) experience.
• Oncology/Hematology TA experience is required.
• ISS & ISE experience is required.
• Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
• Good understanding of the clinical drug development process.
• Strong communication skills and coordination skills.
• Current knowledge of technical and regulatory requirements relevant for the role
• Ability to proactively manage concurrent activities within a project

The following disclaimer for CA must be included (remove the equal opportunities wording from the advert template in the bottom paragraph and replace with the following):

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 theHuman Rights Code and theAccessibility for Ontarians Disabilities Act, in all aspects of the hiring process, upon request by calling + 1 [phone] x 301.

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 theActand will only be used for candidate selection.

#LI-DNP

Apply for this job

*

indicates a required field

First Name *

Last Name *

Email *

Phone *

Location (City) *

Resume/CV *

Enter manually

Accepted file types: pdf, doc, docx, txt, rtf

Enter manually

Accepted file types: pdf, doc, docx, txt, rtf

Education

School * Select...

Degree * Select...

Select...

Start date year *

End date year *

LinkedIn Profile

Website

Are you legally authorized to work in the country that you are being hired? * Select...

If "yes", will you now or in the future require sponsorship to work in the country that you are being hired? * Select...

What type of employment are you seeking? *

Permanent

Subcontractor

Intern

Temporary

Area of expertise - Therapeutic area or other skills

Have you previously worked for ClinChoice or its subsidiaries? If yes, please provide additional details

Do you have a friend or family member working for ClinChoice? If yes, please provide additional details.

Are you currently employed? * Select...

Current Address

Country * Select...

Enter country of residence

Date available to work? *

Employment History: Please list your two most recent employers, including name of the company, job title, and dates employed *

Are you willing to undergo a background check upon employment? * Select...

If hired, can you furnish proof you are eligible to work in the country you are being hired? * Select...

How did you hear about this opening? * Select...

Will you relocate if the job requires it? * Select...

How much are you willing to travel? * Select...

Are you ok to work in a hybrid model work schedule? * Select...

What is your desired salary/hourly rate? (CAD) *

Please read and accept our privacy policy: * Select...

I certify all information provided in this employment application is true and complete. I understand any false information or omission may disqualify me from further consideration for employment and may result in my dismissal if discovered at a later date.

I authorize the investigation of any or all statements contained in this application and also authorize any person, school, current employer (except as previously noted), past employers and organizations’ names in this application to provide relevant information and opinions that may be useful in making a hiring decision. I release such persons and organizations from any legal liability in making such statements.

I understand if I am extended an offer of employment, it may be contingent upon my successfully passing a complete background and reference check. I hereby consent to any or all of these pre-employment test/screen/checks as a condition of employment, if required. I consent to the release of any or all medical information as may be deemed necessary to judge my capability to do the work for which I am applying.

I UNDERSTAND THIS APPLICATION OR SUBSEQUENT EMPLOYMENT DOES NOT CREATE A CONTRACT OF EMPLOYMENT NOR GUARANTEE EMPLOYMENT FOR ANY DEFINITE PERIOD OF TIME.