Clinical Research Associate II

at  Adecco Canada

Adecco is currently hiring for a Clinical Research Associate II for our Medical Manufacturing client in Ottawa West. This opportunity offers full time hours, Monday - Friday. The salary for this position will be determined based on education and experience.
Our client is a diversified health care innovator with a legacy of pioneering work in medical diagnostics and devices. They are dedicated to advancing innovative with patient diagnostic technology to improve patient care and system efficiency by fundamentally changing the way health care professionals process patients through their system.

To qualify for this role, you must have minimum 2 years experience working in conducting clinical studies. The individual must be flexible and be able to work in a fast-paced environment with changing priorities.

• Location: Ottawa, ON
• Shifts: Monday - Friday
• Job type: Full-time | Temporary

QUALIFICATIONS :

• Undergraduate degree or equivalent work experience (Life Sciences, Biochemistry/Chemistry, Nursing, or equivalent)
• Minimum 2 years experience in conducting clinical studies or related laboratory skills
• Understands and follows regulatory and quality standards and specific procedures in executing studies
• Technical or lab experience is of benefit (medical testing, sample handling, point of care invitrodiagnostic experience, etc)
• Strong verbal communication and interpersonal skills
• A mechanical aptitude and good organizational skills
• A keen interest in continuous learning
• Personal attributes: professionalism, adaptability, approachability, enthusiasm, excellent attention to detail, self-motivated, shows initiative and can work effectively as part of a team.
• You must be a self-starter, can follow instructions and use good judgement.
• Must be eligible to work and reside within Canada.
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RESPONSIBILITIES :

• Responsible for execution of general tasks and monitoring tasks of clinical studies
• Carries out timely collection of study documentation according to procedures and regulations
• Carries out monitoring visits, follows up with sites, writes visit reports, etc.
• If needed, participates in the development and maintenance of operating procedures
• Helps to review and document study results
• Participates in the creation of clinical documents which may include protocols/CRFs/reports etc.
• Supports workflow dry runs, contriving, binder prep, etc. onsite in Ottawa and/or clinical sites
• Works collaboratively with teams and can also work independently
• Communicates effectively internally and externally
• Travels to study sites for clinical site visits

To qualify for this role, you must have minimum 2 years experience working in conducting clinical studies. The individual must be flexible and be able to work in a fast-paced environment with changing priorities.

• Location: Ottawa, ON
• Shifts: Monday - Friday
• Job type: Full-time | Temporar