Senior Clinical Trial Assistant / Clinical Research Coordinator

Fortrea; Auckland; On-site; NZD 70,000 - 90,000; Full time

Job summary

A leading company in clinical research seeks a Senior Clinical Trial Assistant for upcoming opportunities. The role involves executing clinical research projects, documentation, and support to ensure high-quality data production. Candidates should have strong communication skills, organizational ability, and a relevant degree or equivalent experience. This position offers a dynamic environment with leadership opportunities and a chance to contribute significantly to clinical trials.

Qualifications

• 2-3 years of relevant Clinical Research experience may be considered.
• Good oral and written communication skills are essential.
• Proven leadership in the CTA group preferred.

Responsibilities

• Document and track study activities using Project Management Systems.
• Assist in preparation of study materials and documentation.
• Train and mentor less experienced Clinical Trial Administrators.

Skills

Communication

Organizational Skills

Critical Thinking

Problem Solving

Computer Literacy

Education

Associate Degree or Equivalent

Tools

Microsoft Office Suite

Job description

Job Overview

The Senior Clinical Trial Assistant (Sr. CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Sr. CTA shall reflect their experience, and the level of contribution which they can make to the project. The CTA performs study-related tasks as required by the department, including (but not limited to): communicate with project team members regarding study updates, maintain documentation as required by protocols, SOPs and regulatory standards, to ensure timely production of high quality clinical data, provide systems support, track information related to the status of study activities and assist with general administrative functions as required. Activities will be conducted in compliance with Company or Sponsor SOPs and regulatory standards and guidelines applicable.

Summary Of Responsibilities

• Document and track study activities using relevant forms and tools and relevant Project Management Systems with minimal guidance and support.
• Assist in the preparation of study and site-specific materials in accordance with relevant SOPs.
• Complete minute taking and documentation for sponsor/external or internal teleconferences as requested.
• Create and maintain tracking systems/spreadsheets for e.g., study supplies.
• Assist with study site invoice payments, budgets and contracts
• Provide support for Investigator Meetings; track meeting attendees and/or other information regarding the Investigator Meeting.
• Provide support to project team (e.g., proof-reading and editing correspondence, large and small documents, mailings, shipment of study files, fax, and photocopy documents, assemble study documents, and arrange meetings, etc.).
• Maintain Trial Master File documentation within the appropriate TMF platform, participate in TMF QC, as assigned, and track and /archive as applicable.
• Audit and CAPA tracking.
• Set up and maintain clinical investigator files and documentation.
• Liaise with vendors, as needed, for study conduct such as printing study materials and/or external systems access for study team members.
• Coordinate and plan study supply shipments with vendors.
• Maintain and confirm shipment information such as courier tracking numbers and date of shipping and delivery.
• Prepare/assemble/ship supplies to sites pre-SIV: Study File Notebooks, CRFs, other study-specific ancillary supplies (i.e., diary cards, patient visit reminders).
• General communications to sponsors, sites and internal team members via electronic mail or courier or telephone.
• Perform other administrative duties
• Train and mentor less experienced Clinical Trial Administrators.
• Liaise with other departments to ensure project delivery.
  
  

Qualifications (Minimum Required)

• Associate degree or equivalent.
• In lieu of the above requirement, candidates with 2-3 or more years of relevant Clinical Research experience in pharmaceutical or CRO industries may be considered.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• Speaking, Writing and Reading in English and local language.
  
  

Experience (Minimum Required)

• Minimum two (2-3) years administrative experience or equivalent training/experience.
• Good oral and written communication skills.
• Proven leadership within the CTA group.
• Good organizational and time management skills.
• Computer literacy (Microsoft Office Suite (Word, Excel, PowerPoint).
• Critical thinking and problem solving.
  
  

Preferred

• Aptitude for handling and proof-reading numerical data, some spreadsheet software competency.
• Good typing skills.
• Good spelling and proof-reading skills.
• Aptitude for handling and reviewing numerical data.
• Ability to operate standard office equipment (e.g., fax, copier).
• Works efficiently and effectively in a matrix environment.
  
  

Preferred Qualifications Include

• Associate degree or equivalent.
  
  

Physical Demands/Work Environment

• Office based in Sydney
  
  

This role is for upcoming future opportunities that may arise at Fortrea

Learn more about our EEO & Accommodations request here.