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Freelance / Contract Clinical Research Associate

Remote: 
Full Remote
Contract: 
Freelance
Experience: 
Mid-level (2-5 years)
Work from: 
Australia

Offer summary

Qualifications:

Prior clinical monitoring in respiratory, Business entity for payment invoicing.

Key responsabilities:

  • Coordinate clinical monitoring ensuring GCP compliance
  • Develop relationships with sites and stakeholders
Atlantic Research Group logo
Atlantic Research Group SME https://www.atlanticresearchgroup.com/
51 - 200 Employees
About Atlantic Research Group
ARG is a contract research organization focused on oncology, immunology and neurology, providing comprehensive clinical program development services ranging from planning to commercialization, achieving over 50 market authorizations to date. Founded in 2004 with the vision that every project should be highly individualized, ARG has experienced consistent growth across the globe, expanding our range to include drug and device strategic consulting, clinical trial management services, as well as clinical data and analytic solutions. ARG uses first-in-class technology platforms along with relationship-driven flexibility to optimize clinical studies because we believe everyone deserves to be well.
See more Atlantic Research Group offers

Job description

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Your missions

Atlantic Research Group (ARG), a distinguished Contract Research Organization (CRO) known for our impactful work in oncology, immunology, and neurology clinical trials, is seeking a Freelance Clinical Research Associate (CRA) to support a respiratory-focused clinical trial across multiple sites in Australia. This role involves monitoring three sites in Melbourne, one in Adelaide, and two in Perth, with a total of 35 subjects enrolled.

Key Responsibilities:

  • Perform and coordinate all aspects of the clinical monitoring process, ensuring compliance with GCPs and ARG's global SOPs.
  • Develop and maintain professional relationships with investigative sites and client company personnel.
  • Represent ARG in the medical research community, enhancing our reputation and contributing to high-quality study outcomes.

Project Timeline:

  • Start Date: October 1, 2024 (or sooner)
  • End Date: Approximately October 30, 2027 (36-month contract)

Qualifications:

  • Prior clinical monitoring experience with a focus on respiratory therapeutic areas.
  • Experience with oncology clinical trials is a bonus.
  • Must have an established business entity to invoice payment. 
  • Ability to travel between Melbourne, Adelaide, and Perth.

If you are a detail-oriented, motivated CRA with experience and are interested in a part-time long-term contract, we would love to hear from you. 

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Spoken language(s):
Check out the description to know which languages are mandatory.

Hard Skills

OncologyClinical Trials

Soft Skills

  • Detail-Oriented
  • Self-Motivation
  • Relationship Management
Are you interested?

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