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    • Biological/ life sciences, pharmacy, chemistry and/or medical or nursing background.
    • Minimum of one year clinical research experience or equivalent.
    • View all Cancer Trials Ireland jobs - Dublin jobs - Clinical Research Associate jobs in Dublin, County Dublin
    • Salary Search: Junior Clinical Research Associate salaries in Dublin, County Dublin
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    • Role is front of house answering queries and dealing directly with patients and other service users.
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    • Meetings, events and functions as required.
    • Westmeath County Council will pay the fee for any general medical examination.
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    • A medical examination, at their own expense, by a qualified medical practitioner nominated by the.
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    • Coordinate and investigate quality events such as deviations, non conformance, product complaints and corresponding action plans including decisions.
    • Support personal matters such as appointments, orders, and events.
    • According to the paychecks, if you are not eligible for corporate medical insurance, the…
    • Minimum 5 years’ experience in GMP production environment, preferably in medical device or pharma industry.
    • Develop and lead the site safety management with a…
    • Must meet medical, physical and security clearance standards, which will be assessed during the recruitment process.
    • On-site Gym or Fitness Discounts.
    • Coordinate consultations between clients and medical consultants.
    • Manage and close sales of high-value medical services.
    • Income protection in the event of illness.
    • Act as a lead coordinator during major incidents and crisis events, ensuring timely mobilisation of response teams.
    • Support new treatment launches, events, promotions and the continued development of the medical side of the business.

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Job Post Details

Junior Clinical Research Associate - job post

Cancer Trials Ireland
Dublin, County Dublin•Hybrid work
€37,000 a year - Full-time

Job details

Pay

  • €37,000 a year

Job type

  • Full-time

Location

Dublin, County Dublin•Hybrid work

Full job description

Key Requirements

1. Biological/ life sciences, pharmacy, chemistry and/or medical or nursing background.

2. Minimum of one year clinical research experience or equivalent.

Main Function(s)

  • Maintain knowledge of ICH-GCP, applicable regulatory requirements and guidelines, SOPs

(Standard Operating Procedures), study protocols and study-specific procedures.

  • Monitor clinical trial sites for assigned studies under the supervision of the study manager or

senior team member in line with ICH-GCP, applicable regulatory requirements and guidelines,

SOPs, study protocols and study-specific procedures.

Primary Responsibilities

  • Perform initiation, monitoring and close out site visits
  • Prepare reports of initiation, monitoring and close-out visits and follow-up on outstanding issues

as per the study monitoring plan.

  • Perform monitoring and reconciliation of Serious Adverse Events (SAEs).
  • Collect and maintain essential documents as required by ICH-GCP, Cancer Trials Ireland and/or

Sponsor SOPs and regulatory requirements/ethics committees.

  • Prepare and review study related documentation as applicable (Patient Information Leaflets,

Informed Consent Forms, Protocols, Case Report Forms and others) under the supervision of the

study manager or senior team member.

  • Communicate on study issues internally at Cancer Trials Ireland and/or with Sponsor (if applicable)

and with Investigator and site staff.

  • Track clinical trial activities.
  • Assist with training, mentoring and development of new and junior staff members.

Meet regularly with the Clinical Project Manager/Trial Coordinator for assigned studies to

review/update on the status of studies regularly and upon request.

  • Input into SOP development where appropriate.
  • Contribute to preparation for audits and inspections as required.
  • Organise and attend Investigator meetings if applicable.
  • Prepare and make presentations as required.
  • Perform other tasks as specified by COM.
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