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CTA Job at Everest Clinical Research | Apply for a Clinical Trial Assistant Opportunity in Canada

CTA Job at Everest Clinical Research | Apply Now

CTA job opportunities in Canada are growing rapidly, especially in the clinical research and life sciences sector. Everest Clinical Research is currently hiring for the position of Everest Clinical Research Clinical Trial Assistant I in Markham, Ontario, Canada. This exciting life sciences job offers candidates the opportunity to work with a globally recognized contract research organization (CRO) supporting pharmaceutical, biotechnology, and medical device industries.

  • Job Position: Clinical Trial Assistant I
  • Job Category: Clinical Operations
  • Job ID: CLINI002649
  • Job Type: Full-Time
  • Location: Markham, Ontario, Canada – Remote

About the Company

CTA job seekers looking for a fast-growing CRO opportunity may find Everest Clinical Research an excellent place to build their career. Everest Clinical Research is a full-service contract research organization (CRO) that provides expertise-based clinical research services to pharmaceutical, biotechnology, and medical device industries worldwide.

Founded in 2004, Everest has developed a strong reputation for high-quality deliverables, flexibility, and superior customer service. The company operates from its headquarters in Markham, Ontario, Canada, with additional locations in the United States, China, and Taiwan. Everest continues to grow rapidly in the clinical research industry while supporting advanced drugs, biologics, and medical devices currently in development.

CTA Job Description

CTA job responsibilities at Everest Clinical Research involve supporting clinical trial operations while ensuring compliance with ICH-GCP guidelines and local regulations.

The Clinical Trial Assistant I will interact with study sponsors, investigational sites, vendors, and internal functional groups to support efficient and high-quality clinical trial operations. The role also includes assistance with regulatory documentation, maintenance of Trial Master Files (TMF), Clinical Trial Management Systems (CTMS), and support for site management activities. This life sciences job also includes coordinating study documentation, supporting investigator meetings, managing shipment and tracking of trial materials, maintaining study portals, and assisting with reports, invoices, and compliance activities.

Qualifications

CTA job applicants should meet the following qualifications:

  • Bachelor’s degree in Life Sciences or related field
  • Excellent verbal and written communication skills
  • Strong computer proficiency
  • Expert knowledge of Microsoft Office Suite
  • Minimum 1 year of administrative support experience preferred
  • Experience maintaining electronic TMFs
  • Thorough understanding of ICH-GCP guidelines and regulations
  • Ability to travel up to 5% of working hours

Salary and Benefits

Estimated Salary Range: $45,000 – $65,000 annually

Benefits Include:

  • Medical, dental, and vision coverage
  • Life and AD&D insurance
  • Short-term and long-term disability coverage
  • Tuition reimbursement
  • Fitness reimbursement
  • Employee Assistance Program (EAP)
  • Pension plan
  • Paid time off and sick leave
  • Performance-based bonus opportunities

Key Responsibilities – CTA Job

CTA job responsibilities include:

  • Interact with study Sponsors, investigational sites, vendors, and Everest functional groups
  • Compile documentation for qualification of clinical sites
  • Support review of documentation to ensure compliance with ICH-GCP and local regulations
  • Maintain essential study documentation for inspection readiness
  • Assist with site identification and feasibility activities
  • Support development of Clinical Operations documents
  • Coordinate investigator meetings and departmental meetings
  • Manage shipment and tracking of trial documents and supplies
  • Track monitoring compliance metrics and issue reminders
  • Distribute SUSARs to investigational sites
  • Download and summarize reports from EDC and IWRS systems
  • Compile progress reports for investigational sites
  • Process vendor invoices and investigator payments
  • Support SOP development and training activities
  • Support Requests for Proposals and additional Clinical Operations activities

Why Join Everest Clinical Research?

CTA job opportunities at Everest Clinical Research provide professionals with exposure to global clinical research projects and advanced therapeutics development. Employees work in a collaborative and customer-focused environment that values quality, flexibility, and professional growth.

This life sciences job is ideal for candidates interested in clinical operations, regulatory documentation, TMF management, and clinical trial coordination within a rapidly growing CRO environment.

APPLY ONLINE HERE

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