Adecco is currently hiring a temporary full-time Clinical Research Associate to work for our client a leader in the health care industry, in Ottawa, ON. In this role you will be responsible for understanding clinical study data systems and to carry out all monitoring for clinical studies at clinical sites and remotely. Is also capable of being part of clinical study data reviews, regulatory submissions. This role does require 3-6 years of related work experience and a bachelor’s degree or equivalent with a background in science or a medically related field. If this sounds like you apply today!
Location: Ottawa, ON
Job type: Temporary | Full-time
Here's why you should apply:
4% vacation paid weekly
Paid weekly accurate and on time
Strong health and safety programs
Medical and dental benefits once qualified
Free training programs
New and quicker onboarding process
Ensures compliance with protocol and regulatory policies, procedures and/or guidelines during clinical studies by training/guidance of investigators/study coordinators, and follow-up of corrective actions.
Understands clinical study data systems and is to carry out all monitoring for clinical studies at clinical sites and remotely. Is also capable of being part of clinical study data reviews, regulatory submissions etc.
Ensures validity of study by identifying/resolving discrepancies and obtaining missing data and may track core lab activities and more complex components of the trial.
Contributes to developing and writing clinical protocols, case report forms, and other study aids for investigational products by addressing issues by interacting with appropriate personnel.
Maintains expertise in regulations for applicable geographies and types of studies
Serves as a resource related to clinical trial regulations. May mentor and train new employees.
Ensures timely collection of study documentation by obtaining, maintaining, and controlling all necessary records and documentation according to procedures and regulations.
Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
Travel up to 25% of the time domestically and/or internationally may be required.
Other miscellaneous duties as may be required
Must be legally eligible to work, and reside in Canada
Require 3-6 years relevant work experience.
Bachelor's degree or equivalent required; prefer background in the sciences or a medically related area (such as but not limited to Biology, Chemistry, Nursing, Medical Technology, Respiratory Therapy or related field of study).
Communications skills, both oral and written. Ability to initiate, plan and manage projects/tasks.
Strong decision-making skills and ability to prioritize.
Ability to form and develop interpersonal, professional relationships; display socially and professionally
International Harmonized Committee Good Clinical Practices, IHC/GCP.
Current Good Manufacturing Practice 21 CFR Part 820 is an asset.
Knowledge of project management tools and techniques.
Broad knowledge and application of business concepts, procedures.
Advanced English Oral/Written.
Job requires daily use of basic computer software like MS Office (Word, Excel and PowerPoint) as well as Lotus Notes and Internet.
Intermediate MS Office, SAS JMP.
If you are interested in the Clinical Research Associate position in Ottawa, ON, apply now and an Adecco recruiter will reach out soon!
Adecco is the largest staffing firm in Canada with over 40 locations and our passionate team is dedicated to find you a job you’ll love. We offer one of the best benefits packages in the whole entire staffing industry and we like to have fun at work!
To find out more about Adecco Perks and what we can do for you please visit the link here: https://www.adecco.ca/en-ca/working-with-a-staffing-agency/adecco-perks/
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