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Search Results for Clinical Research Associate
Job Title. Location Salary Actions

Senior Clinical Trials Associate

Senior Clinical Trial Associate Our client, a global biotech organization, are currently expanding their clinical team and are recruiting for a Senior Clinical Trial Associate to work with them on a permanent basis. As Senior Clinical Trial Associate, you’ll play an important role in being responsible for providing assistance to the Clinical Trial Manager on one or more trials in all relevant aspects of trial preparation, trial conduct, documentation and archiving. As Senior Clinical Trial Associate you will be responsible for assisting with setting-up and maintainin...

Location: Dublin,
Senior Clinical Trials Associate
Dublin Not Disclosed

Clinical Trial Start Up Associate - Native Danish

A Danish speaking Trial Capabilities Associate is required to join a leading global pharmaceutical business based in Cork. This is an opportunity to join a vibrant multi-cultural and multi-lingual team where you will play your part in making a difference for people the world over by supporting the business as it discovers, develops, and delivers medicines that help people live longer, healthier and more active lives. The role Initiate investigator site activities, including collection and submission of regulatory documents, customization and negotiation of informed con...

Location: Cork,
Clinical Trial Start Up Associate - Native Danish
Cork Not Disclosed

Clinical Trial Start Up Associate- Hebrew

A Hebrew speaking Clinical Trial Start Up Associate is required to join a leading global pharmaceutical business based in Cork. This is an opportunity to join a vibrant multi-cultural and multi-lingual team where you will play your part in making a difference for people the world over by supporting the business as it discovers, develops, and delivers medicines that help people live longer, healthier and more active lives. The Clinical Trial Start Up Associate is accountable to ensure the investigator sites meet requirements to enroll study participants into clinical trials and suppo...

Location: Cork,
Clinical Trial Start Up Associate- Hebrew
Cork Not Disclosed

Clinical Project Manager

Clinical Project Manager Our client a clinical stage biopharmaceutical organisation, are currently recruiting for a Clinical Project Manager to join their experienced team. As Clinical Project Manager you will coordinate the day-to-day management of the clinical operations activities of the organisation. This is a super opportunity to join an excellent organisation at a very exciting stage. This role also offers hybrid working. Responsibilities Accountable for meeting or exceeding goals for clinical trial operations for development projects Develop and maintain ef...

Location: Dublin,
Clinical Project Manager
Dublin Not Disclosed

Clinical Trials Start up Associate Fluent Spanish

Clinical Trials Start Up Associate Fluent Spanish Our Cork based client are currently recruiting for an experienced fluent Spanish speaking Clinical Trials Associate to join their team on a permanent basis. The Clinical Trial Capabilities Team provides clinical trial capabilities in support of clinical development. As Clinical Trials Associate you will be accountable to ensure the investigator sites meet requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and closeout. You will be responsible for obtaining clinical trial aut...

Location: Cork,
Clinical Trials Start up Associate Fluent Spanish
Cork Not Disclosed

Clinical Trial Start Up Associate - Native Danish

A Danish speaking Trial Capabilities Associate is required to join a leading global pharmaceutical business based in Cork. This is an opportunity to join a vibrant multi-cultural and multi-lingual team where you will play your part in making a difference for people the world over by supporting the business as it discovers, develops, and delivers medicines that help people live longer, healthier and more active lives. The role Initiate investigator site activities, including collection and submission of regulatory documents, customization and negotiation of informed con...

Location: Cork,
Clinical Trial Start Up Associate - Native Danish
Cork Not Disclosed

Clinical Trial Start Up Associate- Hebrew

A Hebrew speaking Clinical Trial Start Up Associate is required to join a leading global pharmaceutical business based in Cork. This is an opportunity to join a vibrant multi-cultural and multi-lingual team where you will play your part in making a difference for people the world over by supporting the business as it discovers, develops, and delivers medicines that help people live longer, healthier and more active lives. The Clinical Trial Start Up Associate is accountable to ensure the investigator sites meet requirements to enroll study participants into clinical trials and suppo...

Location: Cork,
Clinical Trial Start Up Associate- Hebrew
Cork Not Disclosed

Clinical Trials TMF Specialist/Clinical Trials Study Team Associate

Clinical Trials TMF Specialist/Clinical Trials Study Team Associate Our client, a very exciting biopharma start-up are currently expanding their Clinical Trials team and are recruiting for a TMF Specialist/Clinical Trials Study Team Associate to join them on a permanent basis. The ideal candidate will have four years’ TMF management experience, both paper and electronic and naming and filing conventions reviews. Experience using Veeva Vault is essential. 4 day working week is an option for this role. This will be a hybrid working role also. ...

Location: Dublin,
Clinical Trials TMF Specialist/Clinical Trials Study Team Associate
Dublin Not Disclosed

Clinical Trials Recruitment and Retention Associate

Clinical Trials Recruitment and Retention Associate Our client, a global pharm company are continuing to expand their Clinical Trials team and are currently recruiting for a Clinical Trials Recruitment and Retention Associate to join them on a permanent basis. Responsibilities Collaborate with cross functional teams to monitor projects in real time Manage daily issues, track trends, collaborate on solutions. Resolve issues that arise, following through to resolution Manage project deliverables post go-live and ensure ongoing project communication including the conduct ...

Location: Cork,
Clinical Trials Recruitment and Retention Associate
Cork Not Disclosed

Clinical Trials TMF Specialist/Clinical Trials Study Team Associate

Clinical Trials TMF Specialist/Clinical Trials Study Team Associate Our client, a very exciting biopharma start-up are currently expanding their Clinical Trials team and are recruiting for a TMF Specialist/Clinical Trials Study Team Associate to join them on a permanent basis. The ideal candidate will have four years’ TMF management experience, both paper and electronic and naming and filing conventions reviews. Experience using Veeva Volt is essential. This role is ideal for someone who would be interested in working 4 days per week. This w...

Location: Dublin,
Clinical Trials TMF Specialist/Clinical Trials Study Team Associate
Dublin Not Disclosed

Senior Manager Clinical Trials

Senior Manager Clinical Trials Our client, a global pharma organisation are currently recruiting for a Senior Manager to lead their Clinical Trial North America Maintenance team.In this role you be responsible for site maintenance/close-out, site contracts amendments, records management, training, and trial metrics across all therapeutic areas. You will serve as point of contact for Competent Authority, assist in budget and contract negotiation if needed. Additional local responsibilities may be required as needed/appropriate for the local geography, and/or to cover re...

Location: Cork,
Senior Manager Clinical Trials
Cork Not Disclosed

Clinical Trial Start Up Associate - Native Danish

A Danish speaking Trial Capabilities Associate is required to join a leading global pharmaceutical business based in Cork. This is an opportunity to join a vibrant multi-cultural and multi-lingual team where you will play your part in making a difference for people the world over by supporting the business as it discovers, develops, and delivers medicines that help people live longer, healthier and more active lives. The role Initiate investigator site activities, including collection and submission of regulatory documents, customization and negotiation of informed consen...

Location: Cork,
Clinical Trial Start Up Associate - Native Danish
Cork Not Disclosed

Clinical Trial Associate German Speaking (based in Ireland)

Clinical Trial Associate German Speaking (based in Ireland) Our Cork based client are currently recruiting for an experienced fluent German speaking Clinical Trial Associate to join their team on a permanent basis. The Clinical Trial Capabilities Team provides clinical trial capabilities in support of clinical development. As Clinical Trials Associate you will be accountable to ensure the investigator sites meet requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and closeout. You will be responsible for obtaining clini...

Location: Cork,
Clinical Trial Associate German Speaking (based in Ireland)
Cork Not Disclosed

Clinical Trial Associate German Speaking (based in Ireland)

Clinical Trial Associate German Speaking (based in Ireland) Our Cork based client are currently recruiting for an experienced fluent German speaking Clinical

Location: Cork,
Clinical Trial Associate German Speaking (based in Ireland)
Cork Not Disclosed
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Clinical Research Associate Career Profile

Clinical Research Associate


The Clinical Research Associate is tasked with monitoring clinical trials sites in order to ensure that studies are carried in accordance with the study protocol, the company standard operating procedures (SOP), applicable regulations and the principles of ICH - GCP (International Conference on Harmonisation - Good Clinical Practice).

Key Responsibilities


  • Identification of key investigators
  • Assistance in the preparation of regulatory submissions
  • Design patient information sheets and consent forms
  • Coordinate document translation and verification
  • Ensure timely submission of protocol/consent documents/safety reports for Ethics/IRB approval according to local requirements
  • Pre-study and initiation visits
  • Conduct regular monitoring visits in accordance with the trial site monitoring SOP
  • Maintain all files and documentation pertaining to studies
  • Motivate investigators in order to achieve recruitment targets
  • Complete accurate study status reports.
  • Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs
  • Keep the project manager regularly informed
  • Process case record forms to the required quality standards and timelines
  • Ensure the satisfactory close-out of investigator sites
  • Ensure correct archiving of files on completion of a study
  • Co-operate with QA personnel in the conduct of QA audits
  • Participate in feasibility studies for new proposals
  • Maintain patient confidentiality

Qualifications / Experience Required


  • Degree in Life Sciences or Equivalent
  • Ability and willingness to travel at least 50% of the time, both international and local
  • Ability to review and evaluate clinical data
  • Computer literacy desirable
  • Foreign language skills desirable
  • Current full driving license essential
  • Good oral and written communication skills