RecruitNet International Ltd specialises in Healthcare recruitment for Domestic and Overseas candidates for Hospitals Nursing Homes Home care and Community care.
We are hiring a Clinical Trials Manager to a Hospital in Dublin Ireland.
Responsibilities
Oversee the day-to-day management of clinical trials ensuring adherence to timelines budgets resources and deliverables.
Develop and maintain trial management plans study protocols and essential study documentation in line with regulatory and institutional standards.
Lead site selection initiation monitoring and close-out activities across assigned studies.
Build and maintain strong collaborative relationships with academic partners industry sponsors funding agencies regulatory authorities and internal stakeholders.
Monitor study progress identify potential risks or deviations and implement appropriate corrective and preventive actions.
Ensure full compliance with ICH-GCP GDPR and Hospital policies and procedures.
Work closely with cross-functional teamsincluding radiology laboratory data management regulatory quality and medical departmentsto ensure smooth trial operations.
Prepare and present regular study updates performance metrics and reports for internal and external stakeholders including regulatory bodies.
Train mentor and supervise Clinical Research Associates (CRAs) Clinical Trials Nurses and other research staff to ensure quality and consistency in trial conduct.
Collaborate with broader hospital leadership and support departments (quality patient safety finance marketing and clinical partners) to align research goals with institutional priorities
Requirements
Bachelors degree in Life Sciences Nursing Pharmacy or a related field.
Masters degree with a focus on Research Methodology Risk or Compliance is desirable.
Minimum 5 years of clinical research experience in an acute hospital setting including at least 2 years in clinical trial management or a leadership role.
Proven experience in the strategic development of clinical research within a hospital or academic setting.
Strong understanding of ICH-GCP guidelines National Research Ethics Committee (NREC) regulations and EU/international clinical trial standards.
Excellent organizational problem-solving and communication skills.
Ability to manage multiple projects and priorities in a fast-paced environment.
Proficiency in Clinical Trial Management Systems (CTMS) and Microsoft Office Suite.
Experience in Oncology clinical research.
Familiarity with Electronic Data Capture (EDC) systems.
Prior involvement in regulatory submissions (NREC or equivalent).
Benefits
- Fully Funded Private Health Insurance
- Excellent Career Opportunities
Required Skills:
Strong understanding of ICH-GCP guidelines National Research Ethics Committee (NREC) regulations and EU/international clinical trial standards. Excellent organizational problem-solving and communication skills. Ability to manage multiple projects and priorities in a fast-paced environment. Proficiency in Clinical Trial Management Systems (CTMS) and Microsoft Office Suite. Experience in Oncology clinical research. Familiarity with Electronic Data Capture (EDC) systems. Prior involvement in regulatory submissions (NREC or equivalent).
Required Education:
Bachelors degree in Life Sciences Nursing Pharmacy or a related field. Masters degree with a focus on Research Methodology Risk or Compliance is desirable.
RecruitNet International Ltd specialises in Healthcare recruitment for Domestic and Overseas candidates for Hospitals Nursing Homes Home care and Community care.We are hiring a Clinical Trials Manager to a Hospital in Dublin Ireland.ResponsibilitiesOversee the day-to-day management of clinical trial...
RecruitNet International Ltd specialises in Healthcare recruitment for Domestic and Overseas candidates for Hospitals Nursing Homes Home care and Community care.
We are hiring a Clinical Trials Manager to a Hospital in Dublin Ireland.
Responsibilities
Oversee the day-to-day management of clinical trials ensuring adherence to timelines budgets resources and deliverables.
Develop and maintain trial management plans study protocols and essential study documentation in line with regulatory and institutional standards.
Lead site selection initiation monitoring and close-out activities across assigned studies.
Build and maintain strong collaborative relationships with academic partners industry sponsors funding agencies regulatory authorities and internal stakeholders.
Monitor study progress identify potential risks or deviations and implement appropriate corrective and preventive actions.
Ensure full compliance with ICH-GCP GDPR and Hospital policies and procedures.
Work closely with cross-functional teamsincluding radiology laboratory data management regulatory quality and medical departmentsto ensure smooth trial operations.
Prepare and present regular study updates performance metrics and reports for internal and external stakeholders including regulatory bodies.
Train mentor and supervise Clinical Research Associates (CRAs) Clinical Trials Nurses and other research staff to ensure quality and consistency in trial conduct.
Collaborate with broader hospital leadership and support departments (quality patient safety finance marketing and clinical partners) to align research goals with institutional priorities
Requirements
Bachelors degree in Life Sciences Nursing Pharmacy or a related field.
Masters degree with a focus on Research Methodology Risk or Compliance is desirable.
Minimum 5 years of clinical research experience in an acute hospital setting including at least 2 years in clinical trial management or a leadership role.
Proven experience in the strategic development of clinical research within a hospital or academic setting.
Strong understanding of ICH-GCP guidelines National Research Ethics Committee (NREC) regulations and EU/international clinical trial standards.
Excellent organizational problem-solving and communication skills.
Ability to manage multiple projects and priorities in a fast-paced environment.
Proficiency in Clinical Trial Management Systems (CTMS) and Microsoft Office Suite.
Experience in Oncology clinical research.
Familiarity with Electronic Data Capture (EDC) systems.
Prior involvement in regulatory submissions (NREC or equivalent).
Benefits
- Fully Funded Private Health Insurance
- Excellent Career Opportunities
Required Skills:
Strong understanding of ICH-GCP guidelines National Research Ethics Committee (NREC) regulations and EU/international clinical trial standards. Excellent organizational problem-solving and communication skills. Ability to manage multiple projects and priorities in a fast-paced environment. Proficiency in Clinical Trial Management Systems (CTMS) and Microsoft Office Suite. Experience in Oncology clinical research. Familiarity with Electronic Data Capture (EDC) systems. Prior involvement in regulatory submissions (NREC or equivalent).
Required Education:
Bachelors degree in Life Sciences Nursing Pharmacy or a related field. Masters degree with a focus on Research Methodology Risk or Compliance is desirable.
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