Hamilton, On Clinical research associate Jobs – 9 Openings This Week

Global Study Leader
Jazz Pharmaceuticals —Mississauga, ON
- $140,000–$210,000 a year
- Microsoft Outlook
- Bachelor's
- Team management
- Dental care
- Vision care
5d
Clinical Research Coordinator (RN)
Cardio Health Inc. —Mississauga, ON
- $30–$35 an hour
- Part-time
- Microsoft Powerpoint
- Microsoft Word
- CPR Certification
- Dental care
Quick apply
R1558503 Directeur associé, Relations clientèle, gestionnaire de projet – Appareils connectés / Client Relationship Associate Director, Connected Devices PM (Clinical Research)
IQVIA —Mississauga, ON
- $108,500–$155,000 a year
- Full-time
- Remote
- Microsoft Word
- Customer service
- Bachelor's
QA Associate – Biologics - Eurofins CDMO Alphora, Inc.
Eurofins Canada BioPharma —Mississauga, ON
- $70,000 a year
- Immediate opening
- Project management
- Bachelor's
- Continuous improvement
- Designated paid holidays
- Disability insurance
Quick apply
Quality Control Associate (part time)
Nutrasource —Guelph, ON
- $22–$25 an hour
- Part-time
- Microsoft Powerpoint
- English
- Presentation skills
Quick apply
6d
Associate Director, Head of Vivarium Operations CA
AstraZeneca —Hamilton, ON
- $134,756.00–$176,867.25 a year
- Temporary
- Sanitation
- Research
- Master's degree
5d
Consultant associé, Services de conseil et d’analyse / Associate Consultant, Consulting & Analytics Services
IQVIA —Mississauga, ON
- $72,500–$120,900 a year
- Full-time
- Microsoft Powerpoint
- English
- Master's degree
Consultant, Services de conseil et d’analyse / Consultant, Consulting & Analytics Services
IQVIA —Mississauga, ON
- $97,500–$147,500 a year
- Full-time
- Microsoft Powerpoint
- English
- Master's degree

Discover related jobs

Based on your search for clinical research associate jobs.

Clinical Research Assistant
Confidential —Hamilton, ON
Comfortable managing multiple tasks with a high degree of accuracy. This is a one-year contract position* with the possibility of becoming permanent based on…
$18–$23 an hour
Quick apply
Equity Research Associate - Metals & Mining
Canaccord Genuity Corp. —Toronto, ON
A post-secondary degree in Engineering (preferably in Mining), Accounting, Finance or Geology; Support and answer institutional client queries;
$100,000 a year

Show more related jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Clinical Research Coordinator (RN)
Cardio Health Inc. —Mississauga, ON
You must hold a current certification of registration from the College of Nurses of Ontario and maintain membership with the RPNAO or RNAO.
$30–$35 an hour
Quick apply
Clinical Research Associate
OCUGEN OPCO INC —Toronto, ON
Bachelor’s degree in life sciences, nursing, pharmacy, or a related discipline, or an equivalent combination of education and relevant experience.
11d

Show more jobs in cities nearby

I want to receive the latest job alerts for clinical research associate in hamilton, on

By signing in to your account, you agree to Workopolis's Terms of Service and consent to our Cookie and Privacy Policy.

Global Study Leader

Jazz Pharmaceuticals
Mississauga, ON

Apply Now

Job details

5 days ago

Benefits

Dental care
Paid vacation
Vision care

Skills

Financial forecasting
Budgeting and forecasting
Microsoft Outlook
Clinical research
Supplier management experience
Coaching
Bachelor's
Stakeholder coordination
Team management
Risk management
Mentoring
Recruiting
Organizational skills
Document archiving
Budgeting
Cross-functional collaboration
Standard operating procedures (SOPs)
Delegation
Project management experience
Communication skills
Team coordination
Stakeholder relationship building
Cross-functional communication
Project progress tracking
Time management
Stakeholder management

Full job description

If you are a current Jazz employee please apply via the Internal Career site.

Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.

Essential Functions/Responsibilities

In partnership with the study team and internal and external service providers, provides oversight to ensure study delivery and ensure operational excellence.

Delegate tasks to study team members as appropriate.

Lead implementation, execution and management of global Phase I–IV clinical trials.

Lead, facilitate and delegate trial-related meetings, ensuring alignment with cross-functional teams.

Act as a primary point of escalation for cross-functional stakeholders for timely issue resolution and alignment.

Participate in program-level discussions (FMT, GPT), providing clear and timely updates to senior management (as needed).

Develop and execute clinical trial strategies in collaboration with cross-functional teams during the trial lifecycle including tracking and reporting trial progress, risks and mitigation strategies to senior leadership.

Hold overall accountability for the Trial Master File (TMF). Acts as an SME for Clinical Operations related sections.

Lead the development and review of trial—specific plans and essential clinical trial documents.

Review and approve key trial documents including protocols, informed consent forms, monitoring plans, and Clinical Study Reports (CSRs) in line with Standard Operating Procedures (SOPs).

Actively contributes to the operational oversight and strategic direction of assigned studies, including feasibility assessments, planning, vendor selection, patient recruitment strategies, and financial forecasting.

Contribute to the planning and conduct of Investigator Meetings, including driving meeting preparation, presenting trial materials, and supporting effective delivery of key messages.

Identify, assess, and proactively manage risk and contingencies to safeguard timelines, quality and compliance.

Develop, manage and track trial timelines and budgets, in line with projected spend. Estimate, track and critically analyze vendor financial spend on trials.

Accountable for the oversight and management of external service providers and vendors to ensure quality, compliance, and performance.

Oversee trial tracking activities and ensure accurate, timely updates within trial management systems.

Accountable for final approval and oversight of trial documentation archiving in compliance with regulatory and company requirements.

Serves as trial lead and SME during audits and inspections.

Coordinate Investigational Medicinal Product (IMP) shipment authorization with regulatory and clinical supplies functions.

Assist and support data query process.

Perform monitoring visit report review (as required).

Lead and participate in Clinical Operations / Global Clinical Development Operations (GCDO) initiatives (as assigned).

Serves as a Clinical Operations SME in the design and review of processes.

Ensure trial activities are conducted according to GCP and relevant SOPs and in accordance with the agreed timelines and trial protocol.

Leadership / People Management Responsibilities:

Mentor and coach Global Study Managers (GSMs) Clinical Research Associates (CRAs), and Global Study Associates (GSAs) to support professional development.

Lead Clinical Trial Working Groups (CTWGs).

Provide leadership in resolving complex trial issues and escalating risks appropriately.

Manage and maintain high performing clinical teams.

Required Knowledge, Skills, and Abilities

7+ years of clinical research experience, with proven global trial management and portfolio-level oversight with a minimum of 3 years in clinical operations leadership roles.

Excellent organizational skills, time-management and attention to detail.

Excellent written and verbal communication skills and stakeholder management abilities.

Ability to work both independently and collaboratively in a fast-paced environment.

Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint).

Experience with and strong knowledge of Clinical Trial electronic systems (e.g., TMF, Clinical Trial Management System (CTMS), etc.).

Strong knowledge of clinical trial processes, ICH-GCP, and regulatory requirements.

Strong knowledge of regulatory start up process and planning in support of Study Start-Up (SSU).

Proven track record of effectively managing in a cross-functional environment.

Excellent project management skills with a proven track record of managing global, multi-center clinical trials.

Strong leadership and governance experience; ability to influence at senior levels.
10% to 20% Domestic and International travel

Required/Preferred Education and Licenses

Bachelor’s degree, preferably in life sciences, healthcare, or a related field, or equivalent experience.

Advanced degree preferred.

#LI-DM1

Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.

FOR US BASED CANDIDATES ONLY

Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $140,000.00 - $210,000.00

Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.

At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.

The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html.

Apply Now

Refine Your Search

clinical research associate jobs in hamilton, on

Global Study Leader

Clinical Research Coordinator (RN)

R1558503 Directeur associé, Relations clientèle, gestionnaire de projet – Appareils connectés / Client Relationship Associate Director, Connected Devices PM (Clinical Research)

QA Associate – Biologics - Eurofins CDMO Alphora, Inc.

Quality Control Associate (part time)

Associate Director, Head of Vivarium Operations CA

Consultant associé, Services de conseil et d’analyse / Associate Consultant, Consulting & Analytics Services

Consultant, Services de conseil et d’analyse / Consultant, Consulting & Analytics Services

Discover related jobs

Explore jobs in cities nearby

I want to receive the latest job alerts for clinical research associate in hamilton, on

Job seeker tools

Employer Tools

Browse

Stay Connected