Lead Data Manager for Clinical Trials

PSI CRO; Mississauga; On-site; CAD 70,000 - 90,000; Full time

Benefits offered by this job

Career development opportunities

Training and skill growth

Job summary

PSI CRO in Mississauga seeks a Lead Data Manager to oversee data management activities for clinical studies. This role requires at least 3 years of experience in data management and proficiency with EDC systems such as Medidata Rave or Oracle Inform.

You will communicate with project teams, manage data collection and validation, and ensure the quality and accuracy of clinical data. This position is an opportunity to advance your career in clinical research.

Qualifications

• At least 3 years of experience in data management for global EDC studies.
• At least 2 years of experience using CDM/EDC systems.
• Organizational and managerial skills.

Responsibilities

• Primary communication point for project teams regarding clinical data management.
• Coordination of data management activities within clinical projects.
• Conducting training for Assistant Data Managers and investigators.

Skills

Data management in clinical research

Communication skills

Organizational skills

Experience with CDM/EDC systems

Education

College or University degree

Tools

Medidata Rave

Oracle Inform

Job description

Lead Data Manager

The Lead Data Manager will be responsible for all data management activities in large, complex studies under general supervision, or working under minimal supervision on data management activities for small to medium sized projects.

Communication

• Primary communication point for project teams and company departments with regard to clinical data management
• Communication line for clients/vendors for all data management aspects of clinical projects and clinical data management reporting

Data Management

• Coordination of data management activities within clinical projects related to EDC development, data collection, cleaning, reconciliation, database lock, development of final integrated database and generation of final Data Management deliverables.
• Primary responsibility for clinical data management activities within clinical projects, including, but not limited to:
  • Study documents review
  • Data Management plan and other project-specific guidelines and instructions development and review
  • Coordinate/perform user acceptance testing
  • Development of Data Validation Plan/Edit Check Specifications
  • Data entry coordination and supervision, feedback to data entry personnel regarding quality of data entry and other data entry issues
  • Data validation, including automatic and manual data inspections, data discrepancies/deficiencies review and resolution, query generation and resolution, feedback to clinical trial teams regarding quality of data
  • Non-CRF electronic data handling (receiving, archiving, loading into study database, review and resolution of reconciliation issues, feedback to vendors regarding quality of data and other issues)
  • Database edits (paper CRF studies)
  • Manual CRF review (non-medical checks)
  • Clinical database lock
  • Coordination and supervision of processing, dispatch and archiving of CRFs/queries
• Input into design of CRFs and other data collection forms; review Case Report Form design for accuracy and adherence to protocol
• Development of CRF completion guidelines
• Coding medical data with coding dictionaries and coding listings review (Lead DMs with medical/biology background, additional training required)
• SAE reconciliation
• Electronic data transfer (import/export) specifications review and approval

Document Management

• Liaison with Document Center with regard to maintenance of TMF and eTMF

Quality Control

• Database QC checks performance and documentation
• Shared responsibility for preparation and attendance at internal and client/third-party audits/inspections of Data Management
• Shared responsibility for follow-up on and resolution of audit findings pertaining to Data Management

Training

• Training of Assistant Data Managers
• Project-specific training of investigators and clinical team in CRF completion

Corporate/Departmental Assignments

• Investigator Meetings preparation/attendance
• Meetings and teleconferences organized by client/vendor preparation/attendance

Qualifications

• College or University degree or equivalent combination of training and experience that presents the required knowledge, skills and abilities
• At least 3 years of experience of full scope of data management responsibilities in global EDC studies
• At least 2 years of experience using CDM/EDC systems (Medidata Rave or Oracle Inform preferable)
• Project data management experience is a plus
• Organizational and managerial skills

Additional Information

Advance your career in clinical research and develop new skillsets whilst growing with the organization.