Skip to main content
Post your CV and find your next job on Indeed!

Medical Oncology Ireland jobs

Sort by: -
    • Excellent knowledge of medical terminology and clinical monitoring process.
    • A minimum of 2 years of monitoring experience in oncology trials.
    • View all Translational Research in Oncology jobs - Remote jobs - Clinical Research Associate jobs in Remote
    • Salary Search: Clinical Research Associate-Freelance salaries in Remote
    • We are hiring a Healthcare Assistant on a permanent, full-time contract.
    • When working in the Clinical area, the post holder will report to the Clinical Nurse…
    • Full-Time Fixed term or Permanent.
    • Increased salary and training grant.
    • General Registration with the Irish Medical Council.
    • Our models offer excellent opportunities for experienced CRA’s to expand their knowledge and skills.
    • Excellent salary and benefits package.
    • Must hold an in in-date OET/IELTS for up to and including December 2027.
    • Must have at least 4 years’ experience within the last 6 years in an acute setting and…
    • Demonstrate depth and breadth of nursing experience in oncology nursing, as relevant to the role.
    • In the course of your employment you may have access to, or…
    • Full Time – 35 hours, Permanent Contract.
    • Acute hospital post graduate experience desirable.
    • It will include weekend and evening work.
    • This is also a rotating shift position.
    • Maintain and comply with Laboratory Documentation and Computerized Systems Data Integrity requirements.
    • This position will report into the IQA Supervisor and support the Quality Assurance team.
    • Ensure that all products leaving AbbVie Biologics Ballytivnan meet the…
    • Experience in oncology drug development desirable.
    • Exceptional medical, dental and vision benefits by country.
    • Reviews CRO/vendor invoices for accuracy.
    • Depending on your area of experience, you may be working in acute ward nursing, high-dependency care, oncology care, orthopaedics, cardiac procedures, endoscopy…
    • Background in medical sales, the healthcare sector or a hospital setting is essential.
    • Reporting into a dynamic and high-performing sales function, you will…
    • The Basic Grade Medical Physicist will perform radiotherapy treatment planning for radiation oncology patients in line with international best practice and in…
    • The candidate will support the operations leadership team in ensuring best in class operational efficiency and effectiveness.
    • Responsible for implementing and maintaining the effectiveness of the integration of projects and NPI into the AbbVie quality system.

People also searched:

ireland visa sponsorship
ireland,visa sponsorship
irish
italian
medical administration
medical device
medical receptionist
medical secretary
oncology nurse
pharmacist

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

UO0HFxcXYQ

Let Employers Find YouUpload Your Resume