Clinical Trials Assistant

Conteúdo do emprego

LMC Manna Research, IACT Health, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research.

The sites that were formerly known as LMC Manna bring phase I-IV clinical trial services with specialized focuses on endocrine disorders, real world evidence big data research, vaccine research, and primary care studies within Canada at sites across Alberta, Ontario, and Quebec. The sites that were formerly known as IACT Health brings phase I-IV clinical trials in over 30 therapeutic areas such as oncology, cardiology, pulmonology, endocrinology, infectious disease, and pain with wholly owned and integrated clinical research offices in multiple cities in the United States across the Southeast, including Georgia and Virginia. The sites that were formerly known as True North Clinical Research are located in Nova Scotia and specialize in research related to Alzheimer’s disease and conditions related to aging, and are committed to finding new treatments to maintain an improved quality of life for patients through innovation and passion.

Centricity Research is committed to revolutionize research by creating outstanding clinical trial experiences to improve the health of the community today and tomorrow through clinical research.

Currently, our rapidly expanding team and site network is looking for a Clinical Trials Assistantwho can work for us on afull-time permanent basis, supporting our Halifax location.

Responsibilities will include but are not limited to:

• Gain familiarity of protocols and case report forms
• Support with the creation and quality control of source documents to be used during the conduct of the clinical research study
• Perform accurate, complete, and timely data entry of electronic or paper case report forms (CRFs)
• Assist Clinical Research Recruitment team in chart screening, database query reviews, and support screening as needed
• Assist Clinical Research Coordinators in responding to data management queries, monitor findings, and follow-up
• Assist Clinical Research Coordinators in the creation, maintenance, update, and organization of the Investigator Site File, ensuring compliance to GCP and LMC SOP/WP
• Prepare research and subject binders and files, as required
• Perform receipt, storage, and organization of Investigational Products
• Perform role of un-blinded research staff (e.g. managing Investigational Product dispensation) if required by site and protocol
• Archive clinical research documents, track, and maintain all archived documents upon completion of a study
• Assess overall filing, documentation, reporting, and archiving processes on an on-going basis to identify improvement opportunities and to assist in implementing process improvements
• Assist QMS team with on-site quality control
• Perform other administrative and clerical duties as required by Clinical Research Coordinators, Site Leads, Regulatory Specialist, Investigators and/or other members of the Research team
• Participate in community and company events such as local health fairs, and fundraising events (expectation 1-2 / calendar year)
• Attend regularly scheduled research meetings, Sponsor training or other meetings as required by the study
• Assist in tracking for physician payments
• Manage front desk supervision
  
  

Requirements:

• A healthcare / clinical research diploma (or equivalent experience in a healthcare / clinical research setting)
• Clinical Research Certificate is an asset
• Excellent communication skills (verbal and written)
• Excellent computer skills (MS Word, Excel and Outlook)
• Attention to detail & thoroughness
• Ability to multi task
• Strong organizational skills
• Strong interpersonal skills
• Self-directed
  
  

Centricity 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

Centricity Research values the health and well-being of our employees, clients and patients and as such we have instituted a COVID-19 Mandatory Vaccination policy for all employees. All candidates attending interviews in-person or receiving job offers will be required to provide proof of vaccination

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