Paid Medical Research jobs in Toronto, ON
Sort by: relevance - date
- AbbVieToronto, ON
- $81,000–$131,000 a year
- Full-time
- Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
- A minimum of 50% travel is required.
- 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
Clinical Research Assistant
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $45,000–$70,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Strong verbal and written communication skills with the ability to understand and summarize medical terminology.
- Detail-oriented, customer- and quality-focused.
Principal PK Scientist
Easily applyEverest Clinical ResearchCanada- $130,000–$160,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Experience with medical writing for clinical research, including CSRs, other regulatory submission documents, and scientific publications.
Clinical Safety Data Associate
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $60,000–$80,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Provide medical advice when required to the Clinical Data Managers for their work in reconciling SAEs.
- Perform coding of AEs/medical histories/concomitant…
Clinical Data Management Specialist
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $45,000–$70,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Assist in resolving data coding discrepancies resulting from the coding of medical events, procedures, and medications.
Clinical Trial IWRS Monitor I
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $45,000–$65,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short-…
Clinical Trial IWRS Monitor I
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $45,000–$65,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short-…
Principal Biostatistician
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $150,000–$200,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Participate in the writing of trial protocols and research proposals.
- Provide statistical consultation to medical and clinical trial personnel for the…
Senior Biostatistician
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $110,000–$160,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Assist in research and development of statistical methodologies and processes.
- Provide statistical expertise for design, analysis and reporting of clinical…
View similar jobs with this employerS&C Electric CompanyEtobicoke, ON M9W 1G4- $96,778–$128,225 a year
- Full-time
- Day shift +1
- Employee assistance program
- Flexible Benefit Options, medical 100% paid by S&C.
- The Health & Safety Specialist is responsible for providing Health and Safety guidance and support to the…
Senior Clinical Trial Analytics Monitor I
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $100,000–$120,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- At least five years of experience in clinical research data analytics and BI reporting implementation.
- We offer a robust benefits package to support your health…
Clinical Data Manager
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $60,000–$95,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Assist in resolving data coding discrepancies resulting from the coding of medical events, treatment procedures, and medications.
Clinical Database Designer I
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $50,000–$100,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Software programming experience relevant to the programming languages and design applications in use in clinical research.
Manager, Clinical Data and Safety Monitoring
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $120,000–$140,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Strong verbal and written communication skills with a demonstrated ability to understand spoken and written medical information and results.
Principal Data Manager
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $130,000–$165,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- Review data, issue queries, and resolve queries from various data sources (e.g., medical coding, medical history, adverse events, procedures and medicinal…
Clinical Trial Web Application Developer
Easily applyEverest Clinical ResearchMarkham, ON L3R 0B8- $90,000–$125,000 a year
- Permanent
- Tuition reimbursement
- Paid time off
- Vision care
- Dental care
- Employee assistance program
- Disability insurance
- We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short-…
Get email updates for the latest Paid Medical Research jobs in Toronto, ON
By creating a job alert, you agree to our Terms . You can change your consent settings at any time by unsubscribing or as detailed in our terms.
People also searched:
Career Resources:
Job Post Details
Clinical Research Associate II
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
Job Description
Qualifications
Additional Information
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
Let Employers Find YouUpload Your Resume