Jobs in Canada

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Added 33 mins ago
YS
Data Analyst Activity Manager
Yemen ShortList
Aden
- Full-time
With the support of the Desk Epidemiologist, creating, reviewing and adapting data collection tools according to the project indicators, and coordinating the development, implementation and…
Added 33 mins ago
RI
Awards Coordinator Yemen Aden- National Only
Relief International
Aden
- Full-time
Support the Grant Manager in the critical review of project progress and implementation, ensuring tracking against proposal targets/donor commitments through reporting preparation and…
Added 33 mins ago
ES
Project Manager – Construction and Energy Efficiency - Toronto
Equans Services Canada & US
Toronto, ON
- Full-time
Equans is looking for a Project Manager - Construction and Energy Efficiency at Toronto!
Added 33 mins ago
LP
Manager, Payroll - Canada
LVMH Perfumes & Cosmetics
Toronto, ON
- Full-time
LVMH HR Shared Services North America is seeking a Payroll Manager to lead and strengthen our Canada payroll and tax operations. This role provides dedicated leadership for eight Canadian…
Added 1 hour ago
IO
Senior Manager, Venture Community (13-Month Term)
Invest Ottawa
Ottawa, ON
- Hybrid
SENIOR MANAGER, COMMUNITY ENGAGEMENT (13 Month Term)
Added 1 hour ago
VC
Project Manager I, People
Vancouver Coastal Health
Vancouver, BC
- $46.39 to $66.68 CAD / hour
- Temporary
Come work as a Project Manager 1 with Vancouver Coastal Health (VCH)!
Added 1 hour ago
VC
Property and Asset Management Coordinator
Vancouver Coastal Health
Vancouver, BC
- $32.44 to $46.64 CAD / hour
- Full-time
Reporting to the Manager, the Property and Asset Management Coordinator is a key member of the Facilities Planning and Real Estate team, and is critical in ensuring the success of managing…
Added 1 hour ago
VC
Property and Asset Management Manager
Vancouver Coastal Health
Vancouver, BC
- $46.39 to $66.68 CAD / hour
- Full-time
Reporting to the Senior Manager, Real Estate and Strategic Planning, the Property & Asset Management Manager is a key member of the Facilities Planning and Real Estate team and is critical…
Added 1 hour ago
VC
Injury Prevention Program Leader, Trauma Services
Vancouver Coastal Health
Vancouver, BC
- $46.39 to $66.68 CAD / hour
- Part-time
Work collaboratively with acute and community partners to carry out project plans and achieve objectives related to projects.
Added 1 hour ago
VC
Project Manager I
Vancouver Coastal Health
Richmond, BC
- $46.39 to $66.68 CAD / hour
- Full-time
Come work as a Project Manager I, with Vancouver Coastal Health (VCH)!
Added 1 hour ago
SS
HSE Manager
Smart Sites Consulting
Vaughan, ON
- Full-time
Role Description The Health and Safety Manager is a full-time hybrid role based in Vaughan, ON, with flexibility for some work from home. This role is responsible for developing,…
Added 1 hour ago
BG
Scheduler
Bidell Gas Compression
Calgary, AB
- Full-time
In this role, you will work directly under the guidance of the Manager Projects and supported by Operations Planner to maintain, update, and optimize project schedules and provide input and…
Added 2 hours ago
VC
Quality & Patient Safety Manager
Vancouver Coastal Health
Vancouver, BC
- $55.27 to $79.45 CAD / hour
- Temporary
Come work as a Quality & Patient Safety Manager with Vancouver Coastal Health (VCH)!
Added 2 hours ago
VC
Healthy Environments & Climate Change Analyst
Vancouver Coastal Health
Vancouver, BC
- $38.9 to $55.92 CAD / hour
- Temporary
Report to the Regional Manager, Health Protection, with day-to-day supervision by the Senior Planner, Healthy Environments & Climate Change
Added 2 hours ago
VC
Energy Specialist, Facilities Planning and Real Estate
Vancouver Coastal Health
Vancouver, BC
- $35.37 to $50.85 CAD / hour
- Full-time
Prepare business reports, memos, proposals, business cases and presentations to the Energy Manager or Director to identify best practices.
Added 2 hours ago
S
Sr. Project Manager
SearchLabs
Markham, ON
- Contract
Project delivery experience using both Waterfall and Agile methodologies.
Added 2 hours ago
AA
Project Manager
ABBARCH Architecture Inc.
Canada
- Full-time
Role Description This full-time Project Manager role is a hybrid position based in Canada, with a combination of in-office and work-from-home arrangements. The Project Manager will oversee…
Added 3 hours ago
S
Manager, Planning and Project Controls, BC Health Workday
Sanya’k̓ula
BC · British Columbia, Canada
- Full-time
Manager, Planning & Project Controls, BC Health Workday
Added 3 hours ago
TR
Grant Writing & Management Coordinator
Telescope Recruitment
Toronto, ON
- $55,000 to $65,000 CAD / year
- Full-time
…candidate will be a highly organized, persuasive writer with strong project management skills, capable of balancing multiple deadlines while maintaining meticulous records of funding…
Added 3 hours ago
PH
Manager, Planning and Project Controls, BC Health Workday
Provincial Health Services Authority
BC · British Columbia, Canada
- Full-time
Manager, Planning & Project Controls, BC Health Workday
Added 3 hours ago
A
Senior Project Engineer
ABB
Québec, QC
- Full-time
Assist the project manager with strategic planning, execution, and project cost tracking.
Added 3 hours ago
A
National Segment Manager Climate
ABB
Saint-Laurent, QC
- Full-time
…a market-based strategy including direct, third party, and project sales and enhancing cross-division and cross-region business-led collaborations for the specific market…
Added 4 hours ago
GC
Technical Director
Game Companies
Vancouver, BC
- Full-time
…the engineering team. They direct, oversee, and communicate project engineering efforts while collaborating for feedback with game…
Added 5 hours ago
CT
Senior Glazing Estimator
CSG Talent
Delta, BC
- $110,000 to $150,000 CAD / year
- Full-time
Advanced project estimator skills that include performing engineering calculations, being conversant in engineering nomenclature to effectively communicate with decision makers, engineers,…
Added 5 hours ago
GC
Senior Manager, Compensation
Game Companies
Vancouver, BC
- Full-time
…Director, Global Compensation Partners, and also work as a project team member on compensation programs. You will work a hybrid schedule, with 3 days a week in our Vancouver…

Novotech Global

*Clinical Research Associate (II-SCRA) / Canada

ON, Canada

Full-time

Apply on fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com About employer

Applications open in a new tab.

Job details

Job type: Full-time
Posting language: English
Posted: Nov 9, 2026

Original job description

Role Summary

The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech, and Sponsor. Key responsibility of a CRA is as a site relationship manager ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs.

Key Responsibilities

Responsibilities:

CRAs primary responsibility is to build relationships with Principal Investigators, study co-ordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited, and smooth management of clinical trials.
Foster internal and external customer relationships to ensure focus on efficient, timely and productive project delivery as per study requirements and timelines.
In collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start-Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed.
In collaboration with Regulatory Start-up (RSU) Team, understand the requirements of applicable local and international regulatory requirements as relevant to specific clinical trials.
Ensure recruitment of participants as per the site target. Drive site recruitment and engagement initiatives and prepare site-specific recruitment plan(s) and update as required.
Monitoring of investigational sites as per ICH GCP §5.18 (Monitoring) and the Clinical Monitoring Plan (CMP) for each study. This includes all monitoring visit types across all phases of a clinical trial including Site Selection, Site Initiation, Site Monitoring and Site Close Out, unblinded pharmacy visits, and co monitoring visits. Visits can be conducted either onsite or remote as per CMP.
- Ensure the rights & wellbeing of trial participants are protected, including consent form checks, patient eligibility confirmation, protocol compliance, investigational drug compliance, and review of Adverse Events/SAEs. Ensure safety issues are reported to the sponsor promptly.
- Verify trial data are accurate and complete, ensure CRF data and queries are completed and resolved as per the study timelines documented in the Clinical Monitoring Plan.
- Ensure all study drug is appropriately stored, dispensed, accounted for, and reconciled as per the Clinical Monitoring Plan and the Protocol.
In collaboration with IHCRA or DMA team, ensure the project Trial Master File (TMF) is up to date, current and complete always throughout duration of the study.
Support sites to be always audit and inspection ready.
Ensure all clinical trial management systems are current and up to date at all times with all relevant trial data.
Provide written and verbal site updates (including monitoring visit reports) on study progress to the PM/LCRA according to the study requirements/timelines as documented in the Clinical Monitoring Plan and Sponsor/Novotech SOPs. Escalate all key issues as per Issue Escalation SOP.
Collaborate with IHCRA and Site Contract Associates, as applicable, on-site payments, taking ultimate responsibility on site payments to ensure payment execution as per term stated in Clinical Trial Agreement.
Assist the PM with the development of study related project plans and templates as per study requirements and support tasks as needed for successful study execution.

Qualifications

Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. Preferably experience of working in the research, pharmaceutical industry or a related field per job level as follows:
CRA II: Approximately 1-2 years of Clinical Research Associate experience or equivalent experience (CRA II fast track) in other roles in the Clinical industry.
CRA III: At least 2-3 years of Clinical Research Associate experience in the Clinical industry.
Senior CRA (SCRA): At least 3-5 years of Clinical Research Associate experience in the Clinical industry.
Fluency in French is highly prioritized

Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.

Our team members are passionate about what we do, but we understand work is only one of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.

We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.

We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to talking to you about working at Novotech.

Apply on fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com About employer

More about this job

Responsibilities

The Clinical Research Associate at Novotech Global will serve as the main contact for trial sites, monitoring visits and data accuracy, while keeping studies compliant with regulations and participant safety rules. The role also covers recruitment support, study drug accountability, trial master file upkeep and progress reporting to the project manager.

Requirements

Candidates need a graduate degree in a clinical or life sciences field, good time management, attention to detail, teamwork and computer skills. Preferred experience is 1 to 2 years as a CRA for CRA II, 2 to 3 years for CRA III and 3 to 5 years for Senior CRA, and French fluency is highly prioritized.

Skills

Clinical trial monitoring
ICH GCP
Site management
Relationship building
Source data verification
CRF review and queries
Adverse event reporting
Trial master file management
Investigational product accountability
Regulatory submissions and ethics approval
Recruitment planning
Clinical trial management systems
Site payments
Monitoring visit reporting
Issue escalation
Project planning
Time management
Attention to detail
Teamwork
Computer literacy
French fluency

Benefits

Flexible working options
Paid parental leave
Flexible leave entitlements
Wellness programs
Ongoing development programs

Keywords

Clinical Research Associate
CRA
clinical trials
ICH GCP
site monitoring
clinical monitoring plan
trial master file
TMF
CRF
source data verification
adverse events
SAE
site initiation
site close out
regulatory submissions
pharmaceutical
biotech
clinical research
Canada
French bilingual

Seniority

Mid level

Perks

Flexible hours
Parental leave
Wellness program

Tools

Clinical trial management systems

Languages

English
French

Fields of study

Clinical sciences
Life sciences

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Work requirements

Jobs in Canada