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

Vacancy Medical Information jobs

Sort by: -
    • 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
    • Collaborate with team members within medical writing and cross-functionally.
    • Ability to interpret scientific or clinical information and present it clearly and…
    • Maintain strict confidentiality when handling patient information.
    • Highly organised with the ability to manage large volumes of information accurately.
    • Where necessary accompany Friars to medical appointments.
    • Provide general information on health and lifestyle (e.g. presentation at Guardian and Vicar meetings,…
    • Process and respond to requests for information, repeat prescriptions and medical certs.
    • Type documents such as medical reports.
    • Scan, file and shred documents.
    • We provide reasonable accommodations at every stage of our recruitment process for disabilities, neurodivergence or medical conditions.
  • View similar jobs with this employer
    • Scheduling medical appointments for patients.
    • Fluent English and the ability to relay information to callers in an easily understood manner.
    • We provide reasonable accommodations at every stage of our recruitment process for disabilities, neurodivergence or medical conditions.
  • View similar jobs with this employer
    • You will receive training and support from experienced colleagues.
    • Whether you already have experience in assembly or learned technical skills in another job,…
    • You will receive training and support from experienced colleagues.
    • Whether you already have experience in assembly or learned technical skills in another job,…
    • They will assign key workers to residents and ensure any vulnerable and/or special needs that are identified are monitored and reviewed on a continual basis and…
  • View similar jobs with this employer
    • Ability to maintain confidentially regarding client information.
    • Providing stabilisation and assistance with walking.
    • Assisting with dressing and grooming.
  • View similar jobs with this employer
    • You will receive training and support from experienced colleagues.
    • Whether you already have experience in assembly or learned technical skills in another job,…
    • Communication Skills: Excellent verbal and written communication skills, with the ability to convey complex medical information clearly and empathetically to…
    • You will receive training and support from experienced colleagues.
    • Whether you already have experience in assembly or learned technical skills in another job,…

Job Post Details

Junior Clinical Research Associate - job post

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

Job details

Pay

  • €37,000 a year

Job type

  • Full-time

Location

Dublin, County DublinHybrid 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.
Let Employers Find YouUpload Your Resume