Explore 8 Jobs at ClinChoice

Associate, Regulatory Affairs Consultant

ClinChoice

Markham, Ontario, CA (Hybrid)

Posted 4 days ago

The Formula/Product Compliance Associate Consultant supports regulatory compliance for cosmetic formulas and finished products across global markets. Responsibilities include reviewing ingredients and formulations, maintaining regulatory documentation and databases, supporting safety assessments and regulatory dossiers, and coordinating compliance updates with product and regulatory teams.

Associate Project Manager

ClinChoice

CA (Remote)

Posted 12 days ago

The Associate Project Manager supports planning and delivery of clinical biometrics projects, coordinating cross-functional activities, timelines, milestones, risks, budgets, and scope. The role also supports client and team communications, quality and compliance, and accurate project documentation in a pharmaceutical/CRO environment.

Project Manager - Canada

ClinChoice

CA (Remote)

Posted 12 days ago

The Project Manager oversees biometrics project teams and multiple clinical studies from start-up through closeout, coordinating clients, vendors, and internal functions. Responsibilities include managing timelines, budgets, risks, issues, contracts, team communication, and project delivery, as well as supporting business development and governance activities.

Sr. RA Associate Consultant

ClinChoice

CA (Remote)

Posted 20 days ago

The Senior Regulatory Affairs Associate Consultant will support a client’s regulatory project team by reviewing, creating, and updating technical documentation under EU MDR and other applicable medical device regulations. Responsibilities include regulatory requirements research, document compilation and quality checks, coordination with affiliates and cross-functional teams, and reporting project status; the role is a 12-month contract with possible extension.

Data Manager-Permanent_Hybrid@Ontario,Canada

ClinChoice

Mississauga, Ontario, CA (Hybrid)

Posted a month ago

The Data Manager leads data management activities for clinical trials, from database setup and study conduct through close-out. Responsibilities include developing study data-management documents and eCRF specifications, overseeing testing and data review, reconciling internal and vendor data, coordinating database locks and archiving, and supporting quality, timelines, training, and client satisfaction.

Senior Statistical Programmer Analyst - Permanent Role_Canada

ClinChoice

Mississauga, Ontario, CA (Remote)

Posted a month ago

The Senior Statistical Programmer leads and supports statistical programming for clinical trials, including creating and validating datasets, tables, figures, listings, and CDISC-compliant submission deliverables. The role also oversees programming deliverables and vendors, contributes to study documentation and programming standards, and provides technical guidance while collaborating across teams.

Junior Statistical Programmer Analyst _Permanent Role_(CANADA)

ClinChoice

Mississauga, Ontario, CA (Remote)

Posted a month ago

The Junior Statistical Programmer Analyst supports clinical trial programming work under the guidance of experienced programmers. Responsibilities include developing, validating, and maintaining clinical datasets and submission deliverables using SAS and/or R, following CDISC standards and quality procedures. The role also involves documentation, data processing, quality checks, and collaboration with cross-functional clinical research teams.

Senior Scientist, Risk Management & Safety Surveillance

ClinChoice

CA (Remote)

Posted a month ago

The Senior Scientist, Risk Management & Safety Surveillance is responsible for core pharmacovigilance deliverables, including aggregate safety reports, safety analyses, case-level reviews, and strategic safety documents. The role collaborates with medical safety stakeholders, therapeutic area teams, vendors, and cross-functional groups while supporting risk management, signal evaluation, regulatory responses, and safety management activities.