Data Manager-Permanent_Hybrid@Ontario,Canada

ClinChoice; Mississauga; Hybrid; CAD 117,000 - 145,000; Full time

Job summary

ClinChoice Canada Inc. is seeking a Data Manager to lead data management for clinical trials in a hybrid role in Ontario, Canada. You will oversee database setup, study conduct and close-out, and collaborate with cross-functional teams to meet timelines and deliver high-quality DM deliverables.

The ideal candidate has 3+ years in pharmaceutical data management, strong knowledge of EDC systems (eCRF/CDMS), and excellent communication and training skills to support sites and internal teams.

Qualifications

• 3+ years data management experience in pharmaceutical industry.
• Experience with EDC systems (eCRF/CDMS).
• Follow SOPs, GCP and ICH guidelines.
• Ability to lead a study or data management team.
• Strong documentation and training skills.

Responsibilities

• Lead data management activities and ensure study deliverables meet timelines and quality standards.
• ReviewClinical research documents such as protocols and Case Report Forms.
• Create and review eCRF specifications.
• Develop DM documents (Data Management Plan, Data Validation Plan, eCRF Completion Guidelines).
• Develop edit rules, query logic and messages; provide training to teams and sites.
• Coordinate archiving of study databases and related documents.
• Perform SAE reconciliation and data transfer activities.

Skills

Data management

Communication

Attention to detail

Training

Education

Bachelor’s degree in clinical/pharmacy/biological/mathematical sciences

Nursing degree

Tools

Medidata Rave

Oracle InForm

OpenClinica

Medrio

Job description

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture. We are looking for a dynamic person to join our in-house team as a Data Manager on a permanent basis. This is a hybrid role at Ontario, Canada.

Join our team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!

The Data manager will be responsible for leading data management (DM) activities for clinical trials including database set up, study conduct and close-out. The Data manager will work collaboratively with a cross functional team to maintain project timelines and to deliver high quality DM deliverables. Key responsibilities may include, but are not limited to:

• Lead Data management activities and ensure study deliverables meet timelines and quality standards.
• Review of Clinical research documents (e.g. protocols, Case Report Forms).
• Create and review electronic Case Report Form (eCRF) specifications.
• Develop critical DM documents such as the Data Management Plan, Data Validation Plan, eCRF Completion Guidelines, Data Entry Guidelines and Data Review Plan. Develop edit rules/checks, query logic and query messages.
• Develop User Acceptance Testing Plan and perform testing on data entry screens and edit checks.
• Create and provide training to the clinical team and sites.
• Perform ongoing data review/reconciliation activities and provide metrics and patient trackers to monitor data clean up.
• Perform database lock/unlock and freeze/unfreeze activities as appropriate for statistical review, interim analysis, and final database lock.
• Coordinate the archiving of study databases and related documents
• Create Data Transfer Specifications and perform external vendor reconciliation.
• Perform SAE reconciliation.
• Work to maintain/improve client satisfaction by ensuring high quality service, communication and management of clinical data.

Qualification

• Bachelor’s degree in clinical/pharmacy biological/mathematical sciences or related field or nursing degree.
• Atleast 3 years data management and/or related work experience in a pharmaceutical industry.
• Working knowledge of Clinical research and clinical trial process and related regulatory requirement and terminology.
• Strong knowledge and experience in several Electronic Data capture systems such as Medidata Rave, Oracle InForm, OpenClinica and Medrio.
• Perform duties in compliance with SOPs, GCP and ICH guidelines.
• Ability to prioritize and to adapt quickly in fast-paced and changing industry conditions.
• Ability to lead a study or data management team independently.
• Proactively drive quality and efficiently to meet timelines and milestones to deliver high quality data management deliverables.
• Excellent verbal and written communication skills.
• Proficient in the use of Microsoft office(Outlook, word, excel, powerpoint, etc)

Open Date: 9/29/2026

Close Date: 10/29/2026

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 [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 the Act and will only be used for candidate selection.

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.

Canada Pay Range

$85 - $105 CAD