Clinical Research Feasibility Lead for Multi-Site Trials

ActivMed Practices & Research, LLC.

Burlington

On-site

CAD 52,000 - 70,000

Full time

32 hours ago
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Benefits offered by this job

Health insurance
Dental insurance
Vision insurance
Life insurance
Disability insurance
Health savings account (HSA)
401k plan

Job summary

Alcanza Clinical Research is seeking a Feasibility Coordinator to process site feasibilities across multiple locations. You will support the Business Development team by reviewing study details, identifying investigators, and maintaining site capability documentation.

Ideal candidates bring a high school diploma or equivalent, 2+ years of admin or sales support, and 1+ year in clinical research. Bilingual English/Spanish is a plus, with HIPAA compliance knowledge encouraged.

Qualifications

  • High school diploma or equivalent with 2+ years in admin or sales support, or equivalent.
  • 1+ year of clinical research experience.
  • Bi-lingual English/Spanish is a plus.

Responsibilities

  • Process feasibility for all sites within sponsor/CRO timelines.
  • Review study details and protocol synopsis for feasibility.
  • Identify investigators and site leaders with Business Development.
  • Contact investigators to assess study feasibility and site capabilities.
  • Maintain site capability documentation and CRM records.
  • Input investigator information into Sponsor/CRO databases.
  • Assist in management of upcoming trials pipeline.
  • Attend company trainings and meetings as required.

Skills

MS Office
Organizational skills
Written and verbal communication
Interpersonal skills
Multi-tasking
Integrity and confidentiality
HIPAA compliance
Independent work

Education

High school diploma or equivalent

Tools

CRM systems

Job description

Alcanza Clinical Research is seeking a Feasibility Coordinator to process site feasibilities across multiple locations. You will support the Business Development team by reviewing study details, identifying investigators, and maintaining site capability documentation.

Ideal candidates bring a high school diploma or equivalent, 2+ years of admin or sales support, and 1+ year in clinical research. Bilingual English/Spanish is a plus, with HIPAA compliance knowledge encouraged.

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