Adecco is currently hiring a temporary full-time Clinical Research Associate to work for an innovative, scientifically oriented health care device manufacturer in Ottawa, ON. This role requires you to have strong knowledge of IHC/GCP guidelines and regulatory requirements, excellent communication and organizational skills, attention to detail, flexibility, problem-solving skills, and a passion for clinical research. Don’t delay, apply now!
*This role requires Canadian Education or Degree or WES Certification.
Location: Ottawa, ON
Shifts: Monday to Friday | 8:00 am – 5:00 pm
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 all 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 able 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 (non- significant risk, feasibility, exempt, etc.).
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 or internationally may be required
Other miscellaneous duties as may be required
Must be legally eligible to work, and reside in Canada
Excellent 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 appropriate behavior.
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)
3-6 years related work experience
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
Advanced English Oral/Written.
Basic computer skills and experience with MS Office (Word, Excel and PowerPoint) as well as Lotus Notes and Internet.
Intermediate MS Office, SAS JMP.
Are you interested in this position? Apply now! Our dynamic team of recruiters will reach out if you qualify for this role.
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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