Job Opportunity as a Clinical Research Associate in Canada at IQVIA

By: IQVIA Last update: 2/29/2024

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Deadline 2024-03-25

(Deadline has passed)

Applicant criteria

NationalityNo specific nationality required

SpecialityMedicine, Nursing and Medical Sciences, Science

Skillsمهارات التواصل, مهارات حل المشكلات, مهارات العمل ضمن الفريق

Age

No specific age required

Years of Experience

Gender

Both

Opportunity criteria

Job Type

Full time

Job FieldsHealthcare Jobs

Opportunity FieldMedical Sciences, Science

Job locationCanada

Needed documentsCV, Application form

Opportunity description

IQVIA company offers a job opportunity as a Clinical Research Assistant in Canada. You will be responsible for performing follow-up and site management work to ensure that sites are conducting the study(s) and submitting their data as required by the study protocol, applicable regulations and guidelines, and funders' requirements.

Duties & responsibilities

You will be responsible for:

Conduct follow-up site visits (selection, initiation, monitoring and closing visits) in accordance with the contracted scope of work and good clinical practice.
Manage relevant study protocols and exercises for assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and various issues.
Evaluate the quality and integrity of study site practices related to proper conduct of protocols and adherence to applicable regulations, and escalate quality issues when needed.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, and completing and submitting the Case Report Form (CRF).
Ensure copies/originals (as required) of site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
Create and maintain appropriate documentation regarding site management, monitoring results of visits and work plans by submitting visit reports, creating follow-up letters and other required study documentation.
Collaborate and communicate with study team members to support project implementation when needed.
You may be responsible for supporting the development of the project's staffing plan on a site-by-site basis, if applicable.
You may be responsible for the financial management of the site in accordance with the executed clinical trial agreement and reimbursement of invoices in accordance with local requirements.

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Eligibility criteria

You must have:

Bachelor's degree in a scientific discipline or health care field.
At least two years of experience in field monitoring.
An equivalent combination of education, training and experience may be accepted in lieu of the required degree.
Good knowledge and skills in applying applicable clinical research regulatory requirements.
Knowledge of Good Clinical Practice (GCP) guidelines.
Required computer skills including proficiency in Microsoft Word, Excel, PowerPoint and use of a laptop, iPhone and iPad (where applicable).
Strong written and verbal communication skills.
Proficiency in English.
Organization and problem-solving skills.
Time management skills.
Financial management skills.
Ability to establish and maintain effective working relationships with co-workers, managers, and clients.

About IQVIA:

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. It believes in pushing the boundaries of human science and data science to make the biggest impact possible – to help its customers create a healthier world.

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