Careers

We need to know more about myeloma- what causes it, how to better diagnose it, diagnose it earlier and identify what treatments works best for each individual.

CMRG is a leader in myeloma research, driven by our goal to produce dynamic research so more patients have better outcomes, an excellent quality of life and ultimately a cure. We welcome applicants to join us as we work towards our goal.

CMRG is an equal opportunity employer.

Current Job Postings

Clinical Research Associate/Regulatory

Type of Employment     Full Time/Permanent

Location                             Vaughan, ON

Qualification                     At minimum completion of a Bachelor of Science degree.

Experience                         2 years of oncology clinical research management experience

Skills & Competencies

  • Strong knowledge of Good Clinical Practice/ICH guidelines, regulatory requirements, drug development process and clinical research monitoring procedures.
  • Experience in project and site management
  • Possess initiative and good judgment with the ability to multi-task
  • Excellent organizational and prioritization skills, ability to learn quickly and independently
  • Excellent communication, presentation, interpersonal skills, both written and spoken.
  • Flexibility and the ability to mentor and manage new staff and to handle multiple tasks to meet deadlines delivering high quality work in a dynamic environment.
  • Ability to travel to conduct site monitoring visits
  • Experience in Medidata Rave and CRF development is an asset
  • Professional Affiliations SoCRA or ACRP required. PMP is an asset

Responsibilities

  • Ensure that studies are being conducted in accordance with study protocol, GCP, and SOPs
  • Performing source document verification of CRFs
  • Conducting drug accountability/ reconciliation
  • Collection /Review of CRFs and regulatory documents
  • Identifying/Resolving problems at the study site to ensure subject safety and data quality
  • Conducting pre-investigation, initiation, monitoring and close-out visits
  • Ability to work in a constantly changing environment and a large network of sites
  • Develop and maintain study-specific plans and project reporting documents according to CMRG policies and SOPs as needed
  • Facilitate and preside over meetings with team members and external clients as necessary
  • Track tasks/deliverables to ensure timelines, milestones &/or goals are attained
  • Monitor & report progress as appropriate & resolve issues in a timely manner
  • Act as a resource to research study personnel to provide direction and resolve issues
  • Oversees completion of study activities per protocol.
  • Ensure appropriateness of study subjects, supervise data collection and reporting, ensure adherence to study protocol
  • Ensure that projects are managed in compliance with appropriate rules & regulations and approved SOP.
  • Ensure that all study activities are completed by strictly following Good Clinical Practices (GCP) & the International Conference on Harmonization (ICH)
  • Coordinate manuscript preparation and submission & disseminate information via seminars, lectures, etc.

 

About CMRG

Canadian Myeloma Research Group (CMRG) is a non-profit research organization specializing in research in multiple myeloma. CMRG research  initiatives include interventional drug trials, real-world data research and translational research  complementing the clinical trials. CMRG’ s goal is to advance myeloma research and make the latest treatments available to the Canadian patients.

 

Canadian Myeloma Research Group is an equal opportunity employer.

We welcome you to send your resume to info@cmrg.ca. Please include a cover letter outlining relevant work experience, professional skills, and the position you seek. We appreciate your interest, however, only candidates selected for an interview will be contacted.

 

Biostatistician/ Research Analyst

Type of Employment        Full Time/ Permanent

Location                                Vaughan, ON

Qualification                       Masters or PhD degree in Biostatistics

Experience                             At least 3 years experience as a biostatician

Skills & Competencies 

  •  Must be a self-starter, works independently and manage multiple projects concurrently
  • A working knowledge of SAS and/or R using Python using a Windows platform is essential.
  • Excellent interpersonal skills and problem solving skills
  • At least three (3) year experience in Oncology (preferred) and/or Clinical trials.
  • Proficiency with MS office, Excel and Power Point software required
  • Excellent organization, prioritization skills, good computer skills, ability to learn quickly and work independently
  • Ability to work under pressure with attention to detail
  • Ability to perform duties in a professional and courteous manner and produce high quality work while meeting deadlines
  • Ability to perform multiple concurrent tasks

Responsibilities:

Biostatistician/Research Analyst will support CMRG clinical trials and eCancerCare based clinical database for Multiple Myeloma, Amyloidosis and Other Related Diseases. The responsibilities include

  • Protocol development, sample size calculation, protocol and CRF review, and advise data management on database design and critical data
  • Coordinate the development of analysis plans, table shells, and programming specifications
  • Understand scope of work, budget, and quote assumptions, estimate the work completed, manage scope, and provide revenue and resource forecasts for single studies
  • Consult on operational/statistical/therapeutic area topics
  • Communicate with funder regarding study protocol
  • Act as statistical lead for single complex studies or groups of studies
  • Provide expert statistical input and review of deliverables for validation requirements
  • Review of the clinical study report to ensure statistical integrity in the reporting of the results
  • Interpret analysis and craft statistical sections of integrated reports
  • Provide training and mentoring to team members and department staff as required

About CMRG

Canadian Myeloma Research Group (CMRG) is a non-profit research organization specializing in research in multiple myeloma. CMRG research  initiatives include interventional drug trials, real-world data research and translational research  complementing the clinical trials. CMRG’ s goal is to advance myeloma research and make the latest treatments available to the Canadian patients.

Canadian Myeloma Research Group is an equal opportunity employer.

We welcome you to send your resume to info@cmrg.ca. Please include a cover letter outlining relevant work experience, professional skills, and the position you seek. We appreciate your interest, however, only candidates selected for an interview will be contacted.