Alberta Clinical trial manager Jobs – 9 Openings This Week

Principal IRT Project Manager
Thermo Fisher Scientific —Alberta
- Full-time
- Remote
- English
- Analysis skills
- Project management
3d
Research Ethics Board Specialist
University of Alberta —Edmonton, AB
- Full-time
- Hybrid work
- Customer service
- Microsoft Office
- Master's degree
Quick apply
8h
Clinical Research Coordinator - Genitourinary Group
Alberta Health Services —Edmonton, AB
- $35.34–$45.03 an hour
- Full-time
- Microsoft Office
- Bachelor's
- Computer skills
3d
Bilingual Sr. Clinical Research Associate
Alimentiv —Calgary, AB
- $78,000–$130,000 a year
- Full-time
- Remote
- Bilingual
- English
- Travel
Quick apply
Site Network Manager (North America)
Alimentiv —Calgary, AB
- $97,500–$163,000 a year
- Full-time
- Remote
- Nursing
- Bachelor's
- Travel
Quick apply
10d
Bilingual Clinical Research Associate (CRA)
Medpace, Inc. —Calgary, AB
- Full-time
- Remote
- Bilingual
- English
- Microsoft Office
- Paid time off
- Flexible schedule
12d
Research Coordinator
Prime Site Research Solutions Inc —Edmonton, AB
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Office
- Dental care
Quick apply
Research Assistant
Prime Site Research Solutions Inc —Edmonton, AB
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Office
- Dental care
Quick apply

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Clinical Research Assistant
Everest Clinical Research —Markham, ON
May assist with hardcopy and electronic archiving of clinical trial documents, including filing within a Trial Master File, according to established document…
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Principal IRT Project Manager

Thermo Fisher Scientific
Alberta

Apply Now

Job details

Full-time
3 days ago

Skills

Computer operation
English
Analysis skills
Project management
Bachelor's
Risk management
SharePoint
Computer skills
Communication skills
Negotiation

Full job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join us as a Principal IRT Project Manager – And lead the strategic direction, planning, and execution of Interactive Response Technology (IRT) projects, ensuring their success in pivotal clinical trials.

This is a fully remote opportunity for candidates located in the United States.

What You’ll Do:

Oversee initiatives to develop, optimize and improve departmental processes, associated systems/applications, training and communications to include:
Oversee process improvement initiative teams and/or represents team functions in cross-departmental initiatives; provide mentorship, guidance, support and training for staff and coach teams in developing and implementing process improvement initiatives.
Fulfill role of PDC (Procedural Documentation Coordinator): manage revisions of PPD procedural documents (SOPs/WPDs); updates internal procedural documents (guidance docs, how-to guides, etc.); lead compliance efforts within the department with departmental and PPD processes and associated systems/applications, training and communications; identify training needs and maintain current departmental training matrix; develop and/or approve training materials; lead training sessions.
Lead staff in defining new operational metrics (KPIs, KQIs, KRIs); analyze operational metrics and prepares recommendations.
Review and approve communication methods and materials, including the team intranet sites (corporate Infront site and internal SharePoint site).
Identify and collate information to support prioritization of systems-related business needs and processes and develops recommendations; make recommendations required to prioritize business process improvement needs through quality event CAPA actions, process and systems improvement and optimization, and metrics/trend analyses.
Review/approve audit report responses and ensure deliverables committed to are feasible and within a reasonable due date; provides visibility to management on upcoming/past-due audit deliverables.
Serve as the primary IRT contact for sponsors and study team members during the life of the study including understanding the IRT system requirements and functionality and managing the IRT Vendor in all tasks related to the study.
Partner with functional area leads to identify and evaluate fundamental issues on projects.
Gather information regarding potential or actual risks/issues and provide detailed information to management to ensure the risks/issues are surfaced and mitigated. Manage all IRT quality events that may arise for the study.
Ensure the study is always audit ready. Attend and participate in any study audit that requires IRT attendance.
Perform study specific informal testing, review study specific system support guidelines for accuracy and completeness. Manage the UAT testing phase with all appropriate parties.
Prepare, coordinate, and deliver meeting materials and communications per timeline milestones. Attend/facilitate meetings and communications with sponsors, vendors, and cross-functional team members.
Manage the IRT budget for the life of the study. Ensure accurate hours are included for various tasks. Review and approve all vendor invoices. Escalate any discrepancies or adjustments needed in the IRT budget.

Minimum Requirements:
Education and Experience:

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Effective leadership, project management, and management skills
Excellent judgment, decision making, escalation and risk management skills
Mastery in process development and improvement, especially as it applies to clinical trials and clinical development
Investigative, analytical and creative thinking skills; strong attention to detail
Strong negotiation skills
Expert knowledge of IRT technology and system use
Strong computer skills
Knowledge of the practices, processes and requirements of clinical trials
Knowledge of procedural documents
Ability to think cross-functionally
Excellent interpersonal skills
Effective oral and written communication skills including the ability to communicate in English, both orally and in writing
Demonstrated ability to direct and promote teamwork in a multi-disciplinary and/or multi-cultural team setting
Knowledge of regulatory guidelines and directives

Working Conditions and Environment:

Role is considered home based.
Occasional travel both domestic and international.

Physical Requirements:

Frequently stationary for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Frequent mobility required.
Occasional crouching, stooping, bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacts with others to obtain or relate information to diverse groups.
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.

Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

Apply Now

Refine Your Search

clinical trial manager jobs in alberta

Principal IRT Project Manager

Research Ethics Board Specialist

Clinical Research Coordinator - Genitourinary Group

Bilingual Sr. Clinical Research Associate

Site Network Manager (North America)

Bilingual Clinical Research Associate (CRA)

Research Coordinator

Research Assistant

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