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Oncology Clinical Research Associate (CRA)


This is a Contract position in Toronto, ON posted September 5, 2017.

Posting Title Oncology Clinical Research Associate (CRA) Requisition ID 69790BR Job Category Clinical Research Associate Locations Canada – Montreal, QC
Canada – Ontario
Canada – Quebec
Canada – Toronto, ON
Shift 1 Job Posting Covance is Seeking Oncology Clinical Research Associates (CRAs) in Montreal and Toronto! Up to a $15k sign-on is available!

Up to a $15k sign-on is available!!

This is a unique Clinical Research Associate (CRA) opportunity where you will work within an embedded, Functional Service Provider model with a large name in the industry. This Clinical Research Associate (CRA) role will allow you to work regionally and get in-depth within a set of oncology sister studies.

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities.

As a Clinical Research Associate (CRA) at Covance you will be working on critical clinical trials for large, prominent pharmaceutical companies. As a CRA, you will conduct site monitoring responsibilities for clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Initiation, Routine Monitoring and Close Out Visits. The CRA role will allow you will work on a close-knit team and be mentored by your Manager. At Covance, we know that career development is not one size fits all. We want you to not only succeed – but excel!

Successful candidates will enjoy the benefits of working for a company that values a WORK / LIFE BALANCE!

  • Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit’ targets
  • Join a company where people tend to stay for 6-10 years rather than 1-3
  • Join a genuinely friendly and supportive company where they allow individuals to take ownership of their own performance

See what Covance CRAs have to say:

"The opportunities to grow are one of the top things I like about Covance. Covance really allows you to find a place to be happy. The flexibility of opportunities with Covance is just wonderful."

"One of the things that attracted me to Covance was its longstanding reputation as an industry leader. I consistently hear from sites that Covance is one of their preferred CROs to work with, which speaks volumes about the company’s reputation."

Visit Covance’s CRA microsite to learn more about being a CRA at Covance Education/Qualifications • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure),

  • In lieu of the above education requirement, external candidates with a minimum of 6 years recent clinical monitoring experience will be considered.
  • Valid Driver’s License

Key words: Clinical Research, CRA, SCRA, Clinical Research Associate, GCP, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, CRA II, CRA III, LCRA, Oncology, Cardiovascular, Neuroscience, Immunology, Infectious Diseases, Metabolism, Field Based, Home Based, CRO, Pharmaceutical Experience • 2 years of Clinical Monitoring experience

  • Oncology Monitoring Experience Required EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.