Clinical Trial Investigator

1 hour ago

Central Coast New South Wales, Australia Paratus Clinical Full time $104,000 - $160,000 per year

Do you have a passion for primary care but want to add some variety into your every day? Are you curious about about clinical trials?

Paratus Clinical is a network of high-quality private clinical trial sites, established to meet the increasing need for efficient, cost-effective and quality delivery of clinical trials within Australia particularly in the primary care setting. Sitting outside of the Public Health system, we pride ourselves on our responsiveness to client needs with the speed and quality of the delivery of our client's clinical trials. Our mission is to become the provider of choice for many pharmaceutical companies around the world to deliver their clinical trial for new and novel therapies in areas such as vaccine research, dermatology, rheumatology, haematology, asthma, diabetes, pain, high cholesterol, obesity and many more therapeutic areas.

The Role:

Paratus Clinical Research Central Coast is looking for an enthusiastic Full-Time Clinical Trial Investigator, who is interested in expanding their career in medical research. You will be part of a fantastic team offering a stimulating clinic environment, including flexibility, patient interaction and overseeing and assisting the team in delivering important clinical trials.

Although this position is advertised for Full-Time, Part-Time candidates also encouraged to apply.

This would be suited to a motivated Medical Doctor interested in enhancing their experience with Pharma-sponsored Clinical Trial Research.

The role includes, but is not limited to the following:

  • Conduct medical research in accordance with government regulations, guidelines, ICH Good Clinical Practice and SOPs.
  • Conducting the research as the Principal Investigator (PI) and/or Sub-Investigator (Sub-I).
  • Perform study activities as required by the protocol and applicable regulations.
  • Interpretation of laboratory results, ECG, imaging.
  • Read and understand the informed consent form, protocol, and investigator's brochure.
  • Explain the study to participants and obtain signed informed consent.
  • Follow up and evaluate study participants for the duration of the study.
  • Work proactively with a broader team of Investigators across multiple sites to develop and implement clinical best practice.
  • Assist the Site Operations Manager in smooth day-to-day operations with good communication and a reliable attitude.

Skills & Experience

Essential:

  • Unrestricted AHPRA Medical Practitioner Registration.
  • Not currently listed in the FDA's list "Investigators Ineligible to Receive Investigational New Drugs".
  • High-level computer skills (Microsoft Office, databases and internet/email use).
  • Ability to work independently and as part of a team.
  • Exceptional organisational skills and attention to detail.
  • Ability to handle multiple tasks and meet deadlines.
  • Willingness to learn.
  • Flexible and open to change and excellent problem-solving ability.
  • Vaccinated for COVID-19 and Influenza.
  • Willing to travel to other sites in the Paratus network.

Highly Desirable:

  • Experience in conducting clinical trials or research (ICH-GCP certification) as a Clinical Investigator.
  • Experience working in commercially sponsored trial settings.
  • Experience working in a primary care setting.

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