Brampton On Lead data manager for clinical trials Jobs – 9 Openings This Week

Lead Data Manager for Clinical Trials
PSI CRO —Mississauga, ON
- $115,000–$135,000 a year
- Full-time
- Remote
- Oracle
- Bachelor's
Quick apply
Professional Education Manager - Canada (Hybrid - Ontario, Canada)
Insulet Corporation —Oakville, ON
- $146,050–$187,750 a year
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Bilingual
- Medicine
Associate Director Study Data Manager
AstraZeneca —Mississauga, ON
- $131,520.00–$172,621.05 a year
- Temporary
- Hybrid work
- Nursing
- System design
- Databases
9d
QA Associate – Biologics - Eurofins CDMO Alphora, Inc.
Eurofins Canada BioPharma —Mississauga, ON
- $70,000 a year
- Immediate opening
- Laboratory experience
- Project management
- Bachelor's
- Designated paid holidays
- Disability insurance
Quick apply
8d
Solution Implementation Lead (Connected Devices)
IQVIA —Mississauga, ON
- $104,400–$194,000 a year
- Full-time
- Bachelor's
- Travel
- Leadership
Clinical Screening Coordinator (Regional West)
Centricity Research —Etobicoke, ON
- $40,000–$50,000 a year
- Full-time
- Research
- Bachelor's
- Designated paid holidays
- Dental care
Quick apply
Technical Group Leader, Downstream Manufacturing - Biologics - Eurofins CDMO Alphora, Inc.
Eurofins Canada BioPharma —Mississauga, ON
- $95,000 a year
- Immediate opening
- Engineering
- Laboratory experience
- Master's degree
- Designated paid holidays
- Disability insurance
Quick apply
Director, AI/Digital Product Governance
AstraZeneca —Mississauga, ON
- Bachelor's
- No university degree
- Product management

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Professional Education Manager - Canada (Hybrid - Ontario, Canada)
Insulet Corporation —Oakville, ON
Leads the development and the implementation of the Canadian HCP Education strategy and tactics aligned to commercial business priorities and corporate strategy…
$146,050–$187,750 a year
Tendering/Contracts Clerical Assistant
S. Burnett & Associates Limited —Orangeville, ON
Supporting the Office Administrator when required to assist with general administration duties including: reception, answering phones, filing, scheduling…
$60,000–$70,000 a year
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Manager, Clinical Data Management
Everest Clinical Research —Markham, ON
Function as a technical and operational leader, serve as a Principal level Lead Data Manager for individual clinical trials or a program of clinical trials,…
$140,000–$170,000 a year
Quick apply
Clinical Data Manager
Everest Clinical Research —Markham, ON
A Bachelors’ degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields with at least 2 years experience in clinical trial data…
$60,000–$90,000 a year
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lead data manager for clinical trials jobs near brampton on

Lead Data Manager for Clinical Trials

PSI CRO -
Mississauga, ON

Quick apply

Job details

Full-time
$115,000–$135,000 a year

Qualifications

Oracle
Bachelor's
Data management

Full job description

Company Description

We’re over 3,200+ strong across the globe. We’re scientists, strategists, creatives, and innovators. We value individual brilliance and build a strong foundation for teamwork across all our business. We love the challenge of our industry. We’re changing lives and redefining success every step of the way.

Job Description

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
- Co-ordinate/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.

Quick apply

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lead data manager for clinical trials jobs in brampton on

Lead Data Manager for Clinical Trials

Professional Education Manager - Canada (Hybrid - Ontario, Canada)

Associate Director Study Data Manager

QA Associate – Biologics - Eurofins CDMO Alphora, Inc.

Solution Implementation Lead (Connected Devices)

Clinical Screening Coordinator (Regional West)

Technical Group Leader, Downstream Manufacturing - Biologics - Eurofins CDMO Alphora, Inc.

Director, AI/Digital Product Governance

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