CRA II & Sr. CRAs - Canada - Oncology & Ophthalmology

Fortrea; Toronto; Remote; CAD 65,000 - 90,000; Full time

Job summary

A leading healthcare company is seeking experienced Clinical Research Associates to join their Full Service Outsourcing team in Canada, focusing on oncology and ophthalmology. The successful candidates will monitor clinical trial sites, ensuring adherence to protocols and patient safety, while working in a fast-paced, technology-driven environment. This full-time position offers opportunities for professional growth and contributions to groundbreaking research.

Qualifications

• 1 - 3+ years of Clinical Monitoring experience.
• Oncology or ophthalmology experience is desired.
• Certification in a related allied health profession.

Responsibilities

• Responsible for all aspects of study site monitoring and close-out.
• Ensure adherence to protocol and regulatory requirements.
• Complete Serious Adverse Event (SAE) reporting.

Skills

Clinical Monitoring

Site Management

Data Integrity

Emergency Response

Teamwork

Adaptability

Education

University or college degree in related field

Job description

CRA II & Sr. CRAs - Canada - Oncology & Ophthalmology

Join to apply for the CRA II & Sr. CRAs - Canada - Oncology & Ophthalmology role at Fortrea

CRA II & Sr. CRAs - Canada - Oncology & Ophthalmology

Join to apply for the CRA II & Sr. CRAs - Canada - Oncology & Ophthalmology role at Fortrea

We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team. Oncology or ophthalmology desired, seeking candidates on the East and West Coast of Canada.

What You Will Do

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

Responsibilities

• Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
• Responsible for all aspects of site management as prescribed in the project plans
• General On-Site Monitoring
• Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
• Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
• Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
• Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
• Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
• Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
• Assist with training of new employees, eg. co-monitoring
• Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
• Perform other duties as assigned by management
  
  

Requirements

• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
• 1 - 3+ years of Clinical Monitoring experience
• Oncology or ophthalmology experience is desired
• Open to various hub locations in Canada
  
  

The important thing for us is you are comfortable working in an environment that is:

• Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
• Changing priorities constantly asking you to prioritize and adapt on the spot.
• Teamwork and people skills are essential for the study to run smoothly.
• Technology based. We collect our data directly into an electronic environment.
  
  

- Remote

Applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

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