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Clinical Trials Specialist

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Sydney, New South Wales, Australia beBeeRegulatory Full time $200,000 - $250,000
Job Title: Clinical Research AssociateRole Overview:

The role of a Clinical Research Associate (CRA) is pivotal in ensuring the integrity and quality of clinical trials.

As a CRA, you will be responsible for overseeing various aspects of clinical trial operations, including site management, data collection, and regulatory compliance.

Key Responsibilities:
  • Develop strong relationships with Principal Investigators, study coordinators, and other site personnel to facilitate efficient trial management.
  • Foster collaboration with internal teams, such as In-house Clinical Research Associate (IHCRA) and Regulatory Start Up Associate (RSA), to prepare essential documents and support ethics and regulatory submission processes.
  • Ensure adherence to local and international regulatory requirements, facilitating recruitment of participants as per site targets.
Requirements:
  • Graduate degree in a clinical or life sciences-related field is preferred.
  • Relevant experience/qualifications in allied professions may also be considered.
  • Excellent time management skills, attention to detail, ability to work well in a team, and computer literacy are essential.
Work Environment:

Novotech offers hybrid working arrangements and flexible working hours to promote work-life balance. The organization prioritizes being an employer of choice for gender equality and provides an inclusive work environment.