NETWORK VACANCIES
NETWORK VACANCIES
CURRENT VACANCIES
CURRENT VACANCIES
Validation Officer, Grade 5 College of Medicine, 1 FTE, HRB-CRFG, University of Galway
Summary of Post
Applications are invited for an appointment as Validation Officer (SPC Ref #: 010278)(1 FTE, Grade 5) at CORRIB Research Centre for Advanced Imaging and Core Laboratory and HRB-Clinical Research Facility Galway [HRB-CRFG] at University of Galway.
This post is being offered as a specific purpose contract and will terminate by reason of the expiry of its specific purpose. It is anticipated that the duration of this assignment will be circa 1 year.
Unit College of Medicine Post Title & Subject Area Validation Officer, College of Medicine Post Duration Specific Purpose Contract Level Grade 5 Reports to Head of Programmes, Institute for Clinical Trials The purpose of this role is to lead the validation processes required to verify that the rights and well-being of research participants are protected and that the integrity of the trial data is upheld. The role will be working within a highly qualified team to support the running of Clinical Research, providing Computer System Validation (CSV) and process validation expertise to the CORRIB Research Centre for Advanced Imaging and Core laboratory and the HRB-Clinical Research Facility. This will be achieved by establishing and maintaining key Computer System Validation Processes aligned to a quality management system, reviewing existing electronic systems, advising on the implementation of new systems and effecting CSV and process validation procedures for the units.
The post-holder will report directly to the Head of Programmes, Institute for Clinical Trials, working closely with the Quality Manager(s), Programme Manager(s), Data Management team and Clinical Operations Lead(s).
This is a full time role. Flexible working hours to fulfil the contract hours and the option for hybrid working, in line with University policies, will be considered for this role.
For informal enquiries, please contact CorribCLABfinance@universityofgalway.ie.
Additional information on the CORRIB Research Centre & Core Lab is available at: Corrib Core Lab – University of Galway
Additional information on HRB-CRFG is available at: https://www.universityofgalway.ie/hrbcrfg/services/clinicalresearch/
Information on the University’s Strategic Plan is available at: Strategy | Straitéis 2020-2025 – University of Galway
Salary: €57,931 to €78,536 p.a. pro rata if part time (applicable to new entrants effective from January, 2011) and in accordance with the terms and conditions of the University’s Remuneration policy.
This appointment will be made on the Grade 5 scale in line with current Government pay policy.
Full job spec and further details can be found here.
Closing date for receipt of applications is 17:00 (Irish Time) on Thursday, 18th April 2024. It will not be possible to consider applications received after the closing date.
Garda vetting may apply.
Appointments will be conditional on work authorisation validation. Further details are available at www.dbei.ie
For more information and Application Form please see Jobs – University of Galway Applications should be submitted online.
Please note that appointment to posts advertised will be dependent upon University approval, together with the terms of the Employment Control Framework for the higher education sector.
University of Galway is an equal opportunities employer.
Closing Date
18th April 2024
Research Associate – Clinical Research Nurse (HRB-CRFG), University of Galway
Summary of Post
Applications are invited from suitably qualified candidates for a full-time fixed term appointment as Clinical Research Associate/Research Nurses with the HRB Clinical Research Facility Galway at Galway University Hospitals and the University of Galway (Ref. No. University of Galway 069-24)
The initial post will be for a period of two and a half years, with the potential to extend subject to research funding availability.
The HRB Clinical Research Facility Galway (CRFG) provides the infrastructure, physical space, facilities, expertise and culture needed to support bioscience and medical research. We focus on studies aimed at understanding a range of diseases and translating this knowledge into regulatory approved advances in patient care. Research nurses work with multidisciplinary teams to improve our understanding of a variety of diseases and to develop new tests and treatments to help tackle these diseases. The CRFG aims to provide research participants and patients with the latest advances in areas such as Cancer, Obstetrics and Gynaecology, Paediatrics, Endocrinology, Neurovascular Disease, Critical care, Cardiovascular Disease, Psychiatry, Gastroenterology, Renal Disease, Radiation Oncology, Dermatology and Respiratory Illness. Research undertaken may be interventional (e.g. novel drugs, medical devices) or non- interventional (e.g. registries) and work will be assigned based on the existing and arising needs of the CRFG research programme.
Job Description:
The successful candidate will be part of a multi-disciplinary team who engage with research personnel, interdisciplinary teams and clinicians to support clinical research activities in the CRFG, assisting with the planning, implementation and coordination of clinical research studies.
The purpose of the role is to ensure that the conduct of clinical research studies within the CRFG is in compliance with the currently approved protocol/amendment(s), ensuring adherence to CRFG standard operating procedures (SOP’s), applicable regulations, and the principles of Good Clinical Practice (ICH-GCP).
The research nurses will work under the direction of Principal Investigators (PI) and with a highly qualified team to initiate, screen, recruit, adhere to study and institutional protocols, undertake clinical assessments, manage research data and documentation and support the close out of clinical studies conducted within the CRFG.
Main Duties & Responsibilities:
- Adhere to CRFG SOPs and associated processes for clinical research
- Adhere to nursing procedures within the CRFG and
- Support the setup of clinical research studies in line with CRFG and institutional processes
- Plan and conduct clinical research activities to ensure the smooth operation of each
Study within the CRFG in compliance with the study protocol, ICH-GCP and applicable regulations.
- Participate in the education process of research participants about their disease, clinical research participation plans, gold standard treatment options and outcomes.
- Ensure participants are informed of all details pertaining to the clinical study/research project prior to their
- Screen and contribute to obtaining fully informed consent from participants enrolling into CRFG
- Help to meet study specific target recruitment projections as agreed by sponsor and
- Contribute to the collation of metrics for activities undertaken at the
- Ensure participant confidentiality and dignity is maintained at all times during all study related
- Upkeep of the individual research documentation including site files, case report forms, monitoring arrangements, data correction documentation etc. as they pertain to the CRFG and Study.
- Provide nursing knowledge, expertise, and care to participants participating in study protocols and to nursing and other health care professional colleagues.
- Work within a multi-disciplinary team to evaluate and treat clinical issues in line with research
- Facilitate the ongoing education of multi-disciplinary teams with respect to ICH-GCP, specific study Protocol, and research requirements.
- Ensure continuity of participant and patient care by liaising with outside health professionals and those who are involved with patient clinical care.
- Utilise agreed protocols to deal with referrals and enquiries from other departments/ hospitals/
- Promote a safe clinical environment for research participants, patients, visitors and staff of the
- Undertaking further education as appropriate to the
- Attend investigator meetings (national and international) and educational conferences where applicable
- Any other duties assigned commensurate to this level of post
Qualifications/Skills required:
Essential Criteria
- Successfully completed degree level or equivalent nursing education
- Current registration with an appropriate division of An Bord Altranais
- Have a minimum of 4 years working as a qualified nurse
- Excellent communication skills
- Good problem solving and organizational skills
- Proven ability to work as part of a multi-disciplinary
- Strong IT skills, including MS Office applications
- Competence (or willingness to train) in phlebotomy procedures
Desirable Criteria
- Completed the RCSI level 9 module for clinical research nurses (or equivalent)
- Experience in the field of clinical or translational research and/or other academic studies
- Certified ICH-Good Clinical Practice training
NB: Gárda vetting is a requirement for this post.
Salary: Postdoctoral Researcher/Research Associate Pay scale €42,782 – €54,965 per annum, (subject to the project’s funding limitations), and pro rata for shorter and/or part-time contracts. Default position for all new public sector appointments is the 1st point of the salary scale. This may be reviewed, and consideration afforded to appointment at a higher point on the payscale, where evidence of prior years’ equivalent experience is accepted in determining placement on the scale above point 1, subject to the maximum of the scale.
(Research Salary Scales – University of Galway)
Continuing Professional Development/Training:
Researchers at University of Galway are encouraged to avail of a range of training and development opportunities designed to support their personal career development plans. University of Galway provides continuing professional development supports for all researchers seeking to build their own career pathways either within or beyond academia. Researchers are encouraged to engage with our Researcher Development Centre (RDC) upon commencing employment – see HERE for further information.
Further information on research and working at University of Galway is available on Research at University of Galway
For information on moving to Ireland please see www.euraxess.ie
Further information about HRB Clinical Research Facility Galway is available at https://www.universityofgalway.ie/hrbcrfg/
To Apply:
Applications to include a covering letter, CV, and the contact details of three referees should be sent, via e-mail (in word or PDF only) to crfg@universityofgalway.ie
Please put reference number University of Galway 069-24 in subject line of e-mail application.
Closing date for receipt of applications is extended to 5.00pm (Irish Time) 18th April 2024
A panel may be formed for future posts.
We reserve the right to re-advertise or extend the closing date for this post
All positions are recruited in line with Open, Transparent, Merit (OTM) and Competency based recruitment University of Galway is an equal opportunities employer.
Closing Date
18th April 2024
Validation Officer, Grade 5 College of Medicine, 1 FTE, HRB-CRFG, University of Galway
Summary of Post
Applications are invited for an appointment as Validation Officer (SPC Ref #: 010278)(1 FTE, Grade 5) at CORRIB Research Centre for Advanced Imaging and Core Laboratory and HRB-Clinical Research Facility Galway [HRB-CRFG] at University of Galway.
This post is being offered as a specific purpose contract and will terminate by reason of the expiry of its specific purpose. It is anticipated that the duration of this assignment will be circa 1 year.
Unit College of Medicine Post Title & Subject Area Validation Officer, College of Medicine Post Duration Specific Purpose Contract Level Grade 5 Reports to Head of Programmes, Institute for Clinical Trials The purpose of this role is to lead the validation processes required to verify that the rights and well-being of research participants are protected and that the integrity of the trial data is upheld. The role will be working within a highly qualified team to support the running of Clinical Research, providing Computer System Validation (CSV) and process validation expertise to the CORRIB Research Centre for Advanced Imaging and Core laboratory and the HRB-Clinical Research Facility. This will be achieved by establishing and maintaining key Computer System Validation Processes aligned to a quality management system, reviewing existing electronic systems, advising on the implementation of new systems and effecting CSV and process validation procedures for the units.
The post-holder will report directly to the Head of Programmes, Institute for Clinical Trials, working closely with the Quality Manager(s), Programme Manager(s), Data Management team and Clinical Operations Lead(s).
This is a full time role. Flexible working hours to fulfil the contract hours and the option for hybrid working, in line with University policies, will be considered for this role.
For informal enquiries, please contact CorribCLABfinance@universityofgalway.ie.
Additional information on the CORRIB Research Centre & Core Lab is available at: Corrib Core Lab – University of Galway
Additional information on HRB-CRFG is available at: https://www.universityofgalway.ie/hrbcrfg/services/clinicalresearch/
Information on the University’s Strategic Plan is available at: Strategy | Straitéis 2020-2025 – University of Galway
Salary: €57,931 to €78,536 p.a. pro rata if part time (applicable to new entrants effective from January, 2011) and in accordance with the terms and conditions of the University’s Remuneration policy.
This appointment will be made on the Grade 5 scale in line with current Government pay policy.
Full job spec and further details can be found here.
Closing date for receipt of applications is 17:00 (Irish Time) on Thursday, 18th April 2024. It will not be possible to consider applications received after the closing date.
Garda vetting may apply.
Appointments will be conditional on work authorisation validation. Further details are available at www.dbei.ie
For more information and Application Form please see Jobs – University of Galway Applications should be submitted online.
Please note that appointment to posts advertised will be dependent upon University approval, together with the terms of the Employment Control Framework for the higher education sector.
University of Galway is an equal opportunities employer.
Closing Date
18th April 2024
Research Associate – Clinical Research Nurse (HRB-CRFG), University of Galway
Summary of Post
Applications are invited from suitably qualified candidates for a full-time fixed term appointment as Clinical Research Associate/Research Nurses with the HRB Clinical Research Facility Galway at Galway University Hospitals and the University of Galway (Ref. No. University of Galway 069-24)
The initial post will be for a period of two and a half years, with the potential to extend subject to research funding availability.
The HRB Clinical Research Facility Galway (CRFG) provides the infrastructure, physical space, facilities, expertise and culture needed to support bioscience and medical research. We focus on studies aimed at understanding a range of diseases and translating this knowledge into regulatory approved advances in patient care. Research nurses work with multidisciplinary teams to improve our understanding of a variety of diseases and to develop new tests and treatments to help tackle these diseases. The CRFG aims to provide research participants and patients with the latest advances in areas such as Cancer, Obstetrics and Gynaecology, Paediatrics, Endocrinology, Neurovascular Disease, Critical care, Cardiovascular Disease, Psychiatry, Gastroenterology, Renal Disease, Radiation Oncology, Dermatology and Respiratory Illness. Research undertaken may be interventional (e.g. novel drugs, medical devices) or non- interventional (e.g. registries) and work will be assigned based on the existing and arising needs of the CRFG research programme.
Job Description:
The successful candidate will be part of a multi-disciplinary team who engage with research personnel, interdisciplinary teams and clinicians to support clinical research activities in the CRFG, assisting with the planning, implementation and coordination of clinical research studies.
The purpose of the role is to ensure that the conduct of clinical research studies within the CRFG is in compliance with the currently approved protocol/amendment(s), ensuring adherence to CRFG standard operating procedures (SOP’s), applicable regulations, and the principles of Good Clinical Practice (ICH-GCP).
The research nurses will work under the direction of Principal Investigators (PI) and with a highly qualified team to initiate, screen, recruit, adhere to study and institutional protocols, undertake clinical assessments, manage research data and documentation and support the close out of clinical studies conducted within the CRFG.
Main Duties & Responsibilities:
- Adhere to CRFG SOPs and associated processes for clinical research
- Adhere to nursing procedures within the CRFG and
- Support the setup of clinical research studies in line with CRFG and institutional processes
- Plan and conduct clinical research activities to ensure the smooth operation of each
Study within the CRFG in compliance with the study protocol, ICH-GCP and applicable regulations.
- Participate in the education process of research participants about their disease, clinical research participation plans, gold standard treatment options and outcomes.
- Ensure participants are informed of all details pertaining to the clinical study/research project prior to their
- Screen and contribute to obtaining fully informed consent from participants enrolling into CRFG
- Help to meet study specific target recruitment projections as agreed by sponsor and
- Contribute to the collation of metrics for activities undertaken at the
- Ensure participant confidentiality and dignity is maintained at all times during all study related
- Upkeep of the individual research documentation including site files, case report forms, monitoring arrangements, data correction documentation etc. as they pertain to the CRFG and Study.
- Provide nursing knowledge, expertise, and care to participants participating in study protocols and to nursing and other health care professional colleagues.
- Work within a multi-disciplinary team to evaluate and treat clinical issues in line with research
- Facilitate the ongoing education of multi-disciplinary teams with respect to ICH-GCP, specific study Protocol, and research requirements.
- Ensure continuity of participant and patient care by liaising with outside health professionals and those who are involved with patient clinical care.
- Utilise agreed protocols to deal with referrals and enquiries from other departments/ hospitals/
- Promote a safe clinical environment for research participants, patients, visitors and staff of the
- Undertaking further education as appropriate to the
- Attend investigator meetings (national and international) and educational conferences where applicable
- Any other duties assigned commensurate to this level of post
Qualifications/Skills required:
Essential Criteria
- Successfully completed degree level or equivalent nursing education
- Current registration with an appropriate division of An Bord Altranais
- Have a minimum of 4 years working as a qualified nurse
- Excellent communication skills
- Good problem solving and organizational skills
- Proven ability to work as part of a multi-disciplinary
- Strong IT skills, including MS Office applications
- Competence (or willingness to train) in phlebotomy procedures
Desirable Criteria
- Completed the RCSI level 9 module for clinical research nurses (or equivalent)
- Experience in the field of clinical or translational research and/or other academic studies
- Certified ICH-Good Clinical Practice training
NB: Gárda vetting is a requirement for this post.
Salary: Postdoctoral Researcher/Research Associate Pay scale €42,782 – €54,965 per annum, (subject to the project’s funding limitations), and pro rata for shorter and/or part-time contracts. Default position for all new public sector appointments is the 1st point of the salary scale. This may be reviewed, and consideration afforded to appointment at a higher point on the payscale, where evidence of prior years’ equivalent experience is accepted in determining placement on the scale above point 1, subject to the maximum of the scale.
(Research Salary Scales – University of Galway)
Continuing Professional Development/Training:
Researchers at University of Galway are encouraged to avail of a range of training and development opportunities designed to support their personal career development plans. University of Galway provides continuing professional development supports for all researchers seeking to build their own career pathways either within or beyond academia. Researchers are encouraged to engage with our Researcher Development Centre (RDC) upon commencing employment – see HERE for further information.
Further information on research and working at University of Galway is available on Research at University of Galway
For information on moving to Ireland please see www.euraxess.ie
Further information about HRB Clinical Research Facility Galway is available at https://www.universityofgalway.ie/hrbcrfg/
To Apply:
Applications to include a covering letter, CV, and the contact details of three referees should be sent, via e-mail (in word or PDF only) to crfg@universityofgalway.ie
Please put reference number University of Galway 069-24 in subject line of e-mail application.
Closing date for receipt of applications is extended to 5.00pm (Irish Time) 18th April 2024
A panel may be formed for future posts.
We reserve the right to re-advertise or extend the closing date for this post
All positions are recruited in line with Open, Transparent, Merit (OTM) and Competency based recruitment University of Galway is an equal opportunities employer.
Closing Date
18th April 2024
