Research Scientist

Job type: Full-Time
Accepting BioReady™: Yes
Category: Research and Development
Education: Ph.D.
Experience: 0-3 Years
Employer: Rna Diagnostics
Location: Sudbury, ON
Posted: November 23, 2021
Closes: December 24, 2021

Job Description 

At Rna Diagnostics we have created the RNA Disruption Assay (RDA™); a real-time tool used in the management of cancer chemotherapy.  Working together with our team, this exciting position involves the organization and preparation of regulatory documentation related to GCLP, ISO 13485 and ISO15189 accreditation, management of activities related to ongoing clinical trials and the analysis of RNA samples.  Laboratory work will include cell culture, RNA isolation and analysis, and RNA electropherogram analysis. 

 

Qualifications

PhD in Biology/Biochemistry or related discipline with experience in:

  • Cell culture
  • RNA isolation and analysis
  • Excellent organizational and written communication skills
  • Regulatory experience is considered a strong asset

 

Must be legally entitled to work in Canada

 

Role and responsibilities: 

 

You will assist the company with various aspects of the business including but not limited to:

 

  1. Organize, prepare and file regulatory documentation including SOPs, analytical validation reports, compliance records and all other documentation related to regulatory requirements for medical devices (ISO 13485) and for the purposes of meeting regulatory standards (GCLP, ISO15189)
  2. Plan and carry out experiments for furthering research and development activities related to the company’s RDA assay
  3. Isolate and analyze RNA from a variety of samples using both manual and automated methods
  4. Process clinical samples following SOPs, including running the company’s RDA assay for an ongoing clinical trial
  5. Analyze RNA electropherogram data using our proprietary algorithm
  6. Participate in laboratory management to maintain regulatory standards including performing equipment maintenance, maintaining sample database, follow Health & Safety requirements
  7. Participate in meetings related to the operations of ongoing clinical trials
  8. Read relevant scientific literature to maintain and advance knowledge
  9. Effectively communicate with subordinates, peers and management. Present and interpret potentially complex information and views clearly and concisely in meetings and discussions

 

Please email Cover Letter and CV to:  [email protected] before December 10th, 2021

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