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Clinical Trials Assistant Jobs

Company

LMC Healthcare

Address Toronto, Ontario, Canada
Employment type TEMPORARY
Salary
Category Internet Publishing
Expires 2023-07-21
Posted at 10 months ago
Job Description
LMC|Manna Research is the largest network of fully-owned and integrated clinical research sites in Canada and 3rd largest in North America. We provide Phase I-IV clinical trial services with specialized focuses on endocrine disorders, real world evidence big data research, vaccine research, and primary care studies.


LMC|Manna Research provides Sponsors, CRO’s & ARO’s access to one of the largest fully owned and operated clinical research site networks within Canada at 19 sites across 4 provinces.


Our mission is to improve the health of Canadians today and tomorrow through clinical research.


Currently, our rapidly expanding team is looking for a Clinical Trials Assistant who can work for us on temporary, full time basis for a 6 month contract, supporting our LMC Bayview location.


Responsibilities will include but are not limited to:


  • Complete database query reviews for study candidacy and conduct outbound calls for study interest
  • Obtain and maintain computerized database of all ad callers via the 1 866 telephone line or web postings
  • Work on enrollment and retention initiatives with Manager, Operations and Director of Research
  • Complete screening visits for specified research studies regionally as needed
  • Problem solve and create contingency plans to optimize enrollment via recruitment initiatives
  • Perform receipt, storage and organization of Investigational products
  • Return all phone calls/email responses to interested patients within 24 - 48 hours
  • Provide study metrics on a regular basis and provide ongoing feedback regarding outcome of recruitment initiatives
  • Prepare research and patient binders and files, as required.
  • Assist Clinical Research Coordinators in responding to data management queries, monitor findings and follow-up.
  • Responsible for assessing overall filing, documentation, reporting and archiving processes on an on-going basis at all sites, identify improvement opportunities and assist in implementing process improvements.
  • Accurately complete research tracking log & LMC Manager ad database
  • Identify appropriate study candidacy based on knowledge of each sites recruiting and upcoming clinical trials
  • Responsible for the archiving of clinical research documents upon completion of the study and tracking and maintenance of all archived documents
  • Assist in tracking for physician payments.
  • Assist Clinical Research Coordinators in the creation, maintenance, update and organization of the Investigator Site File, ensuring compliance to GCP and LMC SOP’s.
  • Assist the Director of Research, Manager, Operations and/or Investigators with any other research tasks as required
  • To attend regularly scheduled research meetings, training with Monitors or Sponsor or other meetings as required by the study.
  • Ensure continued QC in the creation and maintenance of source documents, CRF’s (electronic or paper) and Investigator Site File.
  • Assist Clinical Research Recruitment team in chart screening, database query reviews and support screening at clinics as needed.
  • Recruit and screen patients for participation in clinical research studies
  • Perform accurate, complete and timely data entry of electronic or paper case report forms (CRF’s).
  • Perform other administrative and clerical duties as required by Clinical Research Coordinators, Regulatory Specialist, Director or Research, Investigators and/or other members of the Research team.
  • To participate in community and company events such as local health fairs, and fundraising events.
  • Gain familiarity of protocols and case report forms, in order to support creation and QC of source documents to be used during the conduct of the clinical research study.


Requirements:


  • Ability to multi task
  • Strong organizational skills
  • Bachelors of Science Degree or equivalent
  • Excellent communication skills (verbal and written)
  • Attention to detail & thoroughness
  • Access to a reliable vehicle and a valid drivers license to travel to various LMC sites is a must


LMC|Manna Research seeks dynamic individuals who embrace learning and innovation opportunities and those who contribute to improving the health of Canadians today and tomorrow through clinical research.


Why LMC|Manna might be right for you!


  • 2014 and 2015 Canada’s Best Workplaces™
  • 2017 Clinical Researcher of the Year Award (CROY)
  • 2016 Certified Best Workplace™
  • 2017 Site Patient & Recruitment Innovation Award (SPRIA) Winner


Competitive Salary


  • Comprehensive Health Benefits
  • Pension contribution matching
  • State of the art Electronic Medical Records (EMR) environment
  • Ongoing career training and development
  • Additional holiday closures
  • Opportunities to work with internationally renowned Researchers & KOL’s
  • Education allowance (days and funding)
  • Employee Appreciation days off


LMC|Manna Research is committed to meet the accessibility needs of persons with disabilities in a timely manner. These accommodations will be available upon request.


We thank all candidates for their applications, however, only those candidates selected for an interview will be contacted


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