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    • Excellent knowledge of medical terminology and clinical monitoring process.
    • Experience with clinical trial information systems.
    • View all Translational Research in Oncology jobs - Remote jobs - Clinical Research Associate jobs in Remote
    • Salary Search: Clinical Research Associate-Freelance salaries in Remote
    • Immediate availability or short notice period desirable.
    • Degree in Biomedical Science or an equivalent qualification validated by the Academy of Clinical…
    • Work alongside experienced clinical and scientific leaders.
    • A Master's or PhD in a relevant healthcare or scientific discipline with a strong research focus.
    • Bachelor’s degree or higher in a scientific field; advanced degree preferred.
    • Lead or provide input on process improvements.
    • Acts as clinical trial lead on one or two early-phase clinical studies.
    • University degree and relevant clinical trials experience in pharmaceutical, biotech or…
    • Have a degree in Life Sciences or have equivalent experience within a nursing background.
    • Sponsor model has reduced travel (approx. 30% or less) due to using ‘…
    • Interviews will be held as soon as possible after the closing date.
    • Interviews will be held as soon as possible after th.
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    • No bank holiday, weekend or evening work.
    • You will be carrying out home visits to support patients with self-injections or venipuncture.
    • Interviews will be held as soon as possible after the closing date.
    • The timescale may be reduced in exceptional circumstances.
    • Education: Degree in a relevant scientific discipline such as Pharmaceutical Sciences, Chemistry, Biology, Biomedical Engineering, or related field.
    • Experience supporting or working with internationally recruited healthcare or social care staff.
    • This role is central to embedding a culture of safe, compliant…
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    • Minimum 6 months to 1 year of recent nursing experience in Ireland within a GP practice, primary care setting, or any clinical environment.
    • Degree in Chemistry or a related scientific discipline.
    • This role ensures that testing services provided to pharmaceutical and medical device clients are…
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    • Possess a Dentist or Medical Doctor Qualification, with necessary registration IDC (dental council) / IMC (medical council).
    • A higher degree or certification in home healthcare or clinical assessment is preferred.
    • Licensure: Valid nursing license or relevant professional certification…

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Job Post Details

Clinical Research Associate-Freelance - job post

Translational Research in Oncology
4.0 out of 5 stars
Remote
Full-time
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Full-time

Full job description

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.

TRIO is looking for a Clinical Research Associate to join our Monitoring Resource team. Reporting to the CRA Line Manager, this position will be a remote full-time freelance position based in Ireland.

Responsibilities:
  • Performing data verification of source documents;
  • Conducting site visits, including pre-study, initiation, monitoring, and termination;
  • Confirming adherence to all FDA, ICH-GCP, and local regulations;
  • Ensuring implementation and compliance with FDA, and ICH-GCP guidelines
  • Participating in budget negotiation and follow-up where applicable
  • Assisting with data validation and query resolution
  • Mentoring junior team members as required
  • Ensuring the completion and collection of regulatory documents
Qualifications:
  • A minimum of 2 years of monitoring experience in oncology trials
  • Experience monitoring in early-phase trials will be valued.
  • Completion of a science-related Bachelor’s degree
  • Excellent knowledge of medical terminology and clinical monitoring process
  • Strong ICH-GCPs knowledge
  • Experience with clinical trial information systems
  • Ability to travel up to 60% on average
  • Must be legally authorized to work in the country

Prior to applying please review TRIO's Applicant Information Notice

To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.

To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.

Teamwork · Passion · Integrity · Innovation

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