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Paid Clinical Trials jobs in Toronto, ON

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    • Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
    • View all AbbVie jobs - Toronto jobs - Clinical Research Associate jobs in Toronto, ON
    • Salary Search: Clinical Research Associate II salaries in Toronto, ON
    • See popular questions & answers about AbbVie
    • Initialize clinical site data collection and clinical trial partners.
    • As a manager of clinical data collections, you will be responsible for establishing data…
    • To recruit patients for participation in clinical research studies according to research ethics board recommendations.
    • Coordinate with study Project Managers and Clinical Data Managers to maintain high-quality data collected in clinical trials.
    • Experience in Phase I through Phase IV clinical trials with knowledge of drug/medical device regulations and industry standards.
    • Excellent understanding of clinical trials and common clinical trial statistical analysis methods is preferred.
    • Plan and carry out professional development.
    • Maintain and prepare for final archival of data management documentation relevant to the assigned clinical trials and assist the corporate archivist in…
    • Demonstrated experience leading clinical research operations, clinical trials, research governance, ethics and regulatory processes, and quality assurance…
    • Work with a leader of the Statistical Operations management team to manage clinical trial programs/projects from one or multiple clients.
    • 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,…
    • Experience supporting clinical data platforms, clinical technology, data modernization, or analytics transformation initiatives.
    • Demonstrated an in-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical…
    • Clinical trials programmers are highly preferred; exposure/experience in clinical trial statistical programming and/or data analysis is desirable.
    • Demonstrated success building or transforming a clinical trials enterprise in partnership with global industry partners.
    • 1–3 years of experience in clinical study management, with exposure to clinical research project coordination and execution.
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Job Post Details

Clinical Research Associate II
AbbVie
·
3.8
Toronto, ON
•
Remote
$81,000–$131,000 a year
Full-time
Apply on company site

Job details

$81,000–$131,000 a year
Paid time off, Designated paid holidays
Full-time
Remote in Toronto, ON

Full job description

Company Description


About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Our Great Place to Work® Certification highlights our dedication to cultivating a high-trust, and inclusive culture for all.

At AbbVie, you won't just have a job, you’ll have the opportunity to unlock a bright future, because we're not just a workplace; we're a world of possibilities.

Difference makers wanted. Apply now!

What’s In It for You?

  • Innovative work culture
  • Professional development
  • Paid time off: vacation, holidays, personal days, and volunteer days
  • Employee stock purchase
  • Wellness spending account
  • Flexible health insurance
  • Retirement savings programs
  • Bonus plan

Job Description


To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of Clinical Site Management deliverables involving start-up, execution, and close-out of studies.

Key Responsibilities:

  • Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.
  • Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase I to III studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes.
  • Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives. proactively manages the site and ensures action plans are put into place as needed to ensure compliance. Ensures regulatory inspection readiness at assigned clinical sites.
  • Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
  • Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.
  • Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.
  • Manages investigator payments as per executed contract obligations. Negotiates investigator/ hospital agreements with stakeholders. Maintain and complete own expense reports as per local and applicable guidelines.
  • Identifies, evaluates and recommends new/potential investigators/sites on an on going basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.

Qualifications
  • Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred.
  • Minimum of 2 years of clinically-related monitoring experience. Experience in on-site monitoring of investigational drug or device trials is required.
  • Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
  • Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
  • Familiarity with all aspects of study monitoring; data, drug accountability, documentation experience.
  • Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes within the assigned function.
  • Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. Ability to use functional expertise and exercise good judgment.
  • Demonstrated business ethics and integrity.
  • A minimum of 50% travel is required.
  • Proficient with Microsoft Office Suite (Outlook, PowerPoint, Excel, Word, etc.)
  • Must be at ease with technology (the use of various tools/systems to perform day-to-day tasks).
    • Valid driver’s license and passport.


Additional Information


AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

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