236 Clinical Specialist jobs in Ireland

About Teckro

We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.

That's where you come in. We're offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.

Could you be our newest Teckronaut?

What you'll Do:

• Responsible for the training, mentoring and development of CRS Level 1, including the preparation and development of training materials and tools
• Assisting with the updating of clinical operations process guides
• Responsible for quality checking previously developed projects as part of risk assessment
• Involved in the assessment of client documents prior to project development to determine project timelines
• As delegated, will assist in the planning and backlog of projects
• Analyse, understand, and process complex scientific/medical/pharmaceutical information
• Work with study teams and internal project teams to ensure timely delivery of high-quality solutions
• Execute the layout and structure of clinical information required to utilize our products efficiently and effectively
• Monitor, analyze, and action end user feedback and usage analysis metrics to evaluate and improve usability and accuracy of our products
• Successfully complete the 'In-House Clinical Trial Training Programme' delivered by a Senior CRS, covering all aspects of Clinical Trials, including but not limited to: trial design, trial procedures, ICH-GCP, clinical trial regulations, operational activities, safety reporting, monitoring etc. The CRS Level 2 will be deemed competent by both the Senior CRS and CRS Manager.
• Undertake other duties in-line with your role and business requirements as required

Multilingual CRS:

• Assist with translation tasks across various departments within the company
• To perform study demos of Teckro, to join Investigator's Meetings (IMs) and to provide training in local languages to study teams and/or relevant users

The Ideal candidate will have:

• Chinese speaker, with the ability to communicate fluently; including reading, writing, listening and speaking.

• Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro.

• Superb editorial skills with a keen eye for text and graphic layouts

• Strong critical thinking and problem solving skills

• Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands
• Strong interpersonal, verbal and written communication skills
• Superb editorial skills with a keen eye for text and graphic layouts
• Proven ability to organize information in a logical and systematic way
• Ability to focus on fine details and the wider system at the same time
• Extreme attention to detail and accuracy even when balancing multiple projects
• Highly adaptable and flexible

• Ability to quickly and easily switch contexts, particularly between creative and analytical work

• Passion for creative solutions, innovation, and divergent thinking

• Demonstrated ability to work well as part of a team

• Where a candidate is carry out duties in a specific language, proven spoken and written fluency is essential

Qualifications Required:

• At least 18+ months relevant experience with proven competencies in the role.
• Degree in biological science, pharmacy, pharmacology, other health-related field or prior qualifications or experience in technical communications preferred
• Excellent computer skills

Location and Travel:

(Dublin)

• Hybrid role - Dublin City Centre, Ireland.
• Our Dublin City Centre offices are located less than 3 mins for Pearse St Dart Station and beside the Alex Hotel, making it accessible for all major transport.
• We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
• Note: Regrettably we cannot offer work permit sponsorship for this role .To be considered, you must currently be based in Ireland and already hold the necessary legal permissions to work here.

Teckro Benefits:

• 25 days holidays
• Pension
• Healthcare
• Life Insurance
• Share Options
• 50% Maternity leave pay after capped length of service
• Paid Paternity leave scheme
• Bike to Work/ Tax Saver Scheme
• Gym/Wellness Allowance
• Sports and Social Club

We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you

By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro's use of your personal information.

About Teckro

We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.

That's where you come in. We're offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.

Could you be our newest Teckronaut?

What you'll Do:

• Responsible for the training, mentoring and development of CRS Level 1, including the preparation and development of training materials and tools
• Assisting with the updating of clinical operations process guides
• Responsible for quality checking previously developed projects as part of risk assessment
• Involved in the assessment of client documents prior to project development to determine project timelines
• As delegated, will assist in the planning and backlog of projects
• Analyse, understand, and process complex scientific/medical/pharmaceutical information
• Work with study teams and internal project teams to ensure timely delivery of high-quality solutions
• Execute the layout and structure of clinical information required to utilize our products efficiently and effectively
• Monitor, analyze, and action end user feedback and usage analysis metrics to evaluate and improve usability and accuracy of our products
• Successfully complete the 'In-House Clinical Trial Training Programme' delivered by a Senior CRS, covering all aspects of Clinical Trials, including but not limited to: trial design, trial procedures, ICH-GCP, clinical trial regulations, operational activities, safety reporting, monitoring etc. The CRS Level 2 will be deemed competent by both the Senior CRS and CRS Manager.
• Undertake other duties in-line with your role and business requirements as required

Multilingual CRS:

• Assist with translation tasks across various departments within the company
• To perform study demos of Teckro, to join Investigator's Meetings (IMs) and to provide training in local languages to study teams and/or relevant users

The Ideal candidate will have:

• Genuine interest in clinical research, medical advancement and drug and biotechnology development highly beneficial as there is room for advancement within the Clinical Trials area in Teckro.

• Superb editorial skills with a keen eye for text and graphic layouts

• Strong critical thinking and problem solving skills

• Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands
• Strong interpersonal, verbal and written communication skills
• Superb editorial skills with a keen eye for text and graphic layouts
• Proven ability to organize information in a logical and systematic way
• Ability to focus on fine details and the wider system at the same time
• Extreme attention to detail and accuracy even when balancing multiple projects
• Highly adaptable and flexible

• Ability to quickly and easily switch contexts, particularly between creative and analytical work

• Passion for creative solutions, innovation, and divergent thinking

• Demonstrated ability to work well as part of a team

• Where a candidate is carry out duties in a specific language, proven spoken and written fluency is essential

Qualifications Required:

• At least 18+ months relevant experience with proven competencies in the role.
• Degree in biological science, pharmacy, pharmacology, other health-related field or prior qualifications or experience in technical communications preferred
• Excellent computer skills

Location and Travel:

(Dublin)

• Hybrid role - Dublin City Centre, Ireland.
• Our Dublin City Centre offices are located less than 3 mins for Pearse St Dart Station and beside the Alex Hotel, making it accessible for all major transport.
• We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
• Note: Regrettably we cannot offer work permit sponsorship for this role .To be considered, you must currently be based in Ireland and already hold the necessary legal permissions to work here.

Teckro Benefits:

• 25 days holidays
• Pension
• Healthcare
• Life Insurance
• Share Options
• 50% Maternity leave pay after capped length of service
• Paid Paternity leave scheme
• Bike to Work/ Tax Saver Scheme
• Gym/Wellness Allowance
• Sports and Social Club

We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you

By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro's use of your personal information.

We are urgently seeking a 
Clinical Specialist
 to support a leading medical device company on a 
fully remote contract
 through 
December 2025
, with a 
strong possibility of extension
. While this is a remote role, 
Ireland-based candidates
 are preferred to align with the client's team.

The successful candidate will be responsible for 
writing and reviewing Clinical Investigation Plans
, performing 
literature reviews
, and developing 
Clinical Evaluation Protocols
 in compliance with regulatory and clinical standards.

Key Responsibilities:

• Author and review 
  Clinical Investigation Plans
   in collaboration with key stakeholders.
• Conduct detailed 
  literature reviews
   to support clinical evaluation documentation.
• Write and maintain 
  Clinical Evaluation Protocols
   and related technical documents.

Requirements:

• Degree in a 
  life science, medical, or related field
  .
• 10+ years of experience preparing 
  clinical documentation
   for medical device submissions.
• Solid understanding of 
  EU MDR 2017/745
   and relevant clinical evaluation guidance.

Contract Details:

• Rate:
   Competitive hourly rates
• Duration:
   Until 
  December 2025
  , with potential extension.
• Location:
   
  Fully remote
  , ideally 
  Ireland-based
  .

About Teckro

We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.

That's where you come in. We're offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.

Could you be our newest Teckronaut?

What you'll Do:

• Act as a clinical trial advisor and subject matter expert, providing clinical oversight on a multidisciplinary team,
  
  to ensure timely delivery of high quality solutions

• Review study protocols/documents to identify areas of vulnerability and operational importance;
  
  customizing the platform to meet the requirements of individual studies

• Review projects from an End Users perspective to ensure quality, accuracy and relevance before being deployed to the client

• Review/analyze program/study-level risk registers/RACTs to assist in defining 'Engage' messaging campaigns or other use cases for the Teckro platform in order to help client study teams meet study objectives and minimize study risks. Present findings/suggestions to client study teams with support from Project Manager and/or Program Lead/Director for assigned account

• Monitoring/analyzing of platform searches: identification of trends and unanticipated key variables; providing data to the development teams for product improvements.

• Act as a clinical trials resource for the Product team: assisting with testing new functions and providing insight into the day to day work of a clinical research professional.

• Contribute to maintaining and improving in-house templates, SOPs and guides.

• Where required, assist in the training of CRS Level 2 team members to CRS duties giving an in-depth knowledge of what is expected at Level 3.

• Where required, assist in the training and upskilling of CRS Level 3 team members, by mentoring and allowing shadowing of projects and duties.

• Shadowing Level 3 team members as they conduct CRS duties on projects.

• Assist in the induction, training and upskilling of team members, when required.

• Undertake other duties in-line with your role and business requirements as required

• Regularly contribute ideas for innovation and product, quality and process improvements and additions

The Ideal candidate will have:

• Minimum 3 years of clinical operations/clinical research experience within a
  
  hospital or CRO setting (study coordinator, research nurse, CRA/study monitor)

• In dept knowledge of global drug development, clinical trial processes, ICH-GCP, regulations and documentation

• Broad clinical research experience from working within a variety of therapeutic areas preferred.

• Keen interest in technology solutions and Software as a Service (SaaS)

• Experience with clinical operations/industry-related technology solutions and a keen ability to learn new software preferred.

• Strong critical thinking and problem solving skills

• Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands

• Ability to work both independently and in a team-orientated, collaborative environment – able to get the work done, with minimal or no supervision

• Strong interpersonal, verbal and written communication skill

• Results and performance driven

• Adaptable and flexible

• Where a candidate is carry out duties in a specific language, proven spoken and written fluency is essential

Qualifications Required:

• Degree in biological science, nursing, pharmacy or other health-related discipline

• Post graduate qualification in Clinical Research preferred.

• Proven competencies with Clinical Research methodologies and operational day to day activities.

Location and Travel:

(Dublin)

• Hybrid role - Dublin City Centre, Ireland.
• Our Dublin City Centre offices are located less than 3 mins for Pearse St Dart Station and beside the Alex Hotel, making it accessible for all major transport.
• We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
• Note: Regrettably we cannot offer work permit sponsorship for this role .To be considered, you must currently be based in Ireland and already hold the necessary legal permissions to work here.

Teckro Benefits:

• 25 days holidays, entitlement increases with length of service
• Pension
• Healthcare
• Life Insurance
• Share Options
• 50% Maternity leave pay after capped length of service
• Paid Paternity leave scheme
• Bike to Work/ Tax Saver Scheme
• Gym/Wellness Allowance
• Sports and Social Club

We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you

By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro's use of your personal information.

About Teckro

We founded Teckro to simplify and modernize clinical trials. In fact, thousands of clinical trial investigators and research site staff rely on Teckro to make the most informed decisions for their patients.

That's where you come in. We're offering you a role with purpose. Your contribution at Teckro will lead to faster, safer and more efficient clinical trials. Quality of life will be improved. In the end, lives will be saved.

Could you be our newest Teckronaut?

What you'll Do:

• Act as a clinical trial advisor and subject matter expert, providing clinical oversight on a multidisciplinary team,
  
  to ensure timely delivery of high quality solutions

• Review study protocols/documents to identify areas of vulnerability and operational importance;
  
  customizing the platform to meet the requirements of individual studies

• Review projects from an End Users perspective to ensure quality, accuracy and relevance before being deployed to the client

• Review/analyze program/study-level risk registers/RACTs to assist in defining 'Engage' messaging campaigns or other use cases for the Teckro platform in order to help client study teams meet study objectives and minimize study risks. Present findings/suggestions to client study teams with support from Project Manager and/or Program Lead/Director for assigned account

• Monitoring/analyzing of
  
  platform
  
  searches: identification of trends and unanticipated key variables; providing data to the development teams for product improvements.

• Act as a clinical trials resource for the Product team: assisting with testing new functions and providing insight into the day to day work of a clinical research professional.

• Contribute to maintaining and improving in-house templates, SOPs and guides.

• Where required, assist in the training of CRS Level 2 team members to CRS duties giving an in-depth knowledge of what is expected at Level 3.

• Where required, assist in the training and upskilling of CRS Level 3 team members, by mentoring and allowing shadowing of projects and duties.

• Shadowing Level 3 team members as they conduct CRS duties on projects.

• Assist in the induction, training and upskilling of team members, when required.

• Undertake other duties in-line with your role and business requirements as required

• Regularly contribute ideas for innovation and product, quality and process improvements and additions

The Ideal candidate will have:

• Minimum 3
  
  years of clinical operations/clinical research experience within a
  
  hospital or CRO setting (study coordinator, research nurse, CRA/study monitor)
  
  or
  
  at least 18+ months relevant
  
  Teckro CRS Level 3
  
  experience, with proven competencies in the role.

• In dept knowledge of global drug development, clinical trial processes, ICH-GCP, regulations and documentation

• Broad clinical research experience from working within a variety of theraputic areas preferred.

• Keen interest in technology solutions and Software as a Service (SaaS)

• Experience with clinical operations/industry-related technology solutions and a keen ability to learn new software preferred.

• Strong critical thinking and problem solving skills

• Strong multi-tasking and time management skills including the ability to effectively prioritise tasks, depending on timelines and demands

• Ability to work both independently and in a team-orientated, collaborative environment – able to get the work done, with minimal or no supervision

• Strong interpersonal, verbal and written communication skills

• Results and performance driven

• Adaptable and flexible

• Where a candidate is carry out duties in a specific language, proven spoken and written fluency is essential

Qualifications Required:

• Degree in biological science, nursing, pharmacy or other health-related discipline

• Post graduate qualification in Clinical Research preferred.

• Proven competencies with Clinical Research methodologies and operational day to day activities.

Location and Travel:

(Dublin)

• Hybrid role - Dublin City Centre, Ireland.
• Our Dublin City Centre offices are located less than 3 mins for Pearse St Dart Station and beside the Alex Hotel, making it accessible for all major transport.
• We also offer flexible start/ end times, allowing your schedule to suit your lifestyle
• Note: Regrettably we cannot offer work permit sponsorship for this role .To be considered, you must currently be based in Ireland and already hold the necessary legal permissions to work here.

Teckro Benefits:

• 25 days holidays
• Pension
• Healthcare
• Life Insurance
• Share Options
• 50% Maternity leave pay after capped length of service
• Paid Paternity leave scheme
• Bike to Work/ Tax Saver Scheme
• Gym/Wellness Allowance
• Sports and Social Club

We are always looking for amazing people to join our growing team. If you are curious, passionate and motivated, then we want to talk to you

By submitting your application, you agree that Teckro may collect your personal data for recruiting and related purposes. Teckro's Recruitment Privacy Statement explains what personal information Teckro may process, where Teckro may process your personal information, its purposes for processing your personal information, and the rights you can exercise over Teckro's use of your personal information.

Job Description: Clinical Specialist - Physiotherapist

Clinic Name: Resync Physiotherapy

Location: Dublin, Ireland

Position Type: Full-time

About Us: Resync Physiotherapy is a leading private practice clinic dedicated to providing exceptional physiotherapy services to our patients in Dublin and surrounding areas. We pride ourselves on our commitment to evidence-based practice, personalized care, and continuous professional development.

Job Overview: We are seeking a highly skilled and experienced Clinical Specialist - Physiotherapist to join our team and lead in the provision of specialized physiotherapy and rehabilitation. This role will involve advanced clinical practice, mentorship of junior and senior staff, and strategic leadership to drive excellence in patient care and outcomes. The Clinical Specialist will play a pivotal role in shaping the clinical direction of the clinic and contributing to its growth and success.

Responsibilities:

• Provide advanced assessment, diagnosis, and treatment of complex musculoskeletal and/or neurological conditions, utilizing advanced clinical reasoning and specialized interventions.
• Lead the development and implementation of evidence-based treatment and rehab plans for patients with specialized needs, collaborating with interdisciplinary teams to ensure comprehensive and holistic care.
• Serve as a clinical mentor and resource for junior and senior physiotherapists, providing guidance, supervision, and support to enhance clinical skills, professional development, and patient outcomes.
• Conduct ongoing clinical audits and quality improvement initiatives to evaluate and enhance the effectiveness and efficiency of physiotherapy services within the clinic.
• Lead the development and delivery of specialized physiotherapy programs and services, such as chronic pain management, sports rehabilitation, or neurological rehabilitation, based on clinic needs and patient populations.
• Actively participate in research activities, including data collection, analysis, and dissemination of findings, to contribute to the advancement of physiotherapy practice and knowledge.
• Stay abreast of emerging trends, best practices, and innovations in physiotherapy through ongoing professional development, training, and participation in relevant conferences and seminars.
• Collaborate with clinic management to develop and implement strategic initiatives, policies, and protocols to ensure the highest standards of patient care, safety, and satisfaction.

Requirements:

• Masters degree or higher in Physiotherapy from an accredited institution.
• Registration with CORU, ISCP, or another recognized professional body for physiotherapy in Ireland.
• Minimum of 7 years of clinical experience in physiotherapy practice, with a focus on specialized areas such as musculoskeletal rehabilitation or sports rehabilitation.
• Advanced clinical skills and expertise in assessment, diagnosis, and treatment planning for complex patient populations.
• Demonstrated leadership abilities and experience in mentoring and developing clinical staff.
• Professional indemnity insurance coverage.
• Track record of engagement in research activities, including publications, presentations, or involvement in research projects.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with multidisciplinary teams and stakeholders.

Benefits:

• Competitive salary package commensurate with experience and qualifications.
• Opportunities for career advancement and professional development, with a clear pathway for progression to leadership roles.
• Supportive work environment with opportunities for mentorship and collaboration with experienced clinicians.
• Access to ongoing training, conferences, and resources to support clinical excellence and professional growth.
• Employee benefits package, including health insurance, retirement savings options, and flexible scheduling.

At Resync Physiotherapy, we are committed to excellence in physiotherapy practice and the advancement of patient care through innovation, collaboration, and continuous learning. If you are a highly skilled and motivated physiotherapist looking to make a significant impact in specialized areas of practice, we encourage you to apply for this exciting opportunity to join our team as a Clinical Specialist. Let's work together to empower individuals to live healthier, more active lives.

Job Types: Full-time, Permanent

Pay: €55,000.00-€75,000.00 per year

Benefits:

• Company events
• On-site gym
• Sick pay
• Work from home

Work Location: In person

Reference ID: Clinical Specialist

Clinical Specialist Physiotherapist - Sports Surgery Clinic, Santry

Location: SSC Sports Medicine

Job type: Fixed Term

Overview of role:

The Clinical Specialist position offers a unique opportunity to provide clinical leadership and expertise within an interdisciplinary team of specialists. It is focussed on spinal MSK conditions. The role involves assessing and treating injuries, designing and implementing rehabilitation pathways and collaborating with the team to enhance the management of spinal conditions. This position is offered on a temporary basis to cover maternity leave.

Primary Duties and Responsibilities:

Clinical Leadership:

Lead the spinal rehabilitation service, providing expert consultation and joint working with staff to manage patient care through the rehabilitation pathway.

Lead spinal rehabilitation pathway caseload, assessments and delegate referrals appropriately.

Ensure high standards of patient care by implementing evidence-based practices aligned with national and specialist clinical guidance.

Keep staff informed of recent developments through participation in research-based conferences, network meetings, and postgraduate education and training.

Lead team meetings to inform, engage, and motivate team members and to keep staff updated on hospital policies and strategies.

Lead through innovative practice and continuous development of clinical knowledge and skills.

Rehabilitation:

Develop and enhance local pathways of care specifically tailored for spinal rehabilitation patients.

Conduct advanced assessments using investigative and clinical reasoning skills to develop individualised treatment plans.

Evaluate and implement clinical outcome measures to monitor effectiveness of rehabilitation pathways

Management:

Manage and organise your patient caseload and support other therapists with complex spinal rehabilitation cases.

Develop and monitor clinical standards for spinal rehabilitation in accordance with local and national guidelines.

Continuously evaluate and improve the effectiveness of the service through service evaluations and clinical audits in collaboration with the Head of Rehabilitation and relevant stakeholders

Responsible for time management and scheduling of CPD for spinal rehabilitation team members.

Staff Development:

Support and facilitate continuous professional development for team members.

Maintain high clinical standards and support staff through comprehensive in-service training, one-to-one coaching, clinical supervision, and practical sessions.

Promote personal and professional development through regular staff appraisals, and performance reviews.

Participate actively in postgraduate education and organise specialist courses, liaising with local Universities.

Research & Development:

Undertake and support research projects to enhance the evidence base and enhance patient care and service development for the management of spinal rehabilitation.

Communication:

Use advanced communication skills to effectively interact with patients and referrers, ensuring understanding and maximising rehabilitation potential.

Ensure confidentiality in all communications, especially regarding patient, carer, and staff information.

Facilitate clear communication within the multi-professional team to coordinate patient care effectively.

Ensure appropriate record keeping and maintenance of good practice in data recording.

Qualifications & Experience:

Bachelor of Science (Hons) Degree or equivalent

MSc Physiotherapy, Strength and Conditioning, Sports Science

Registrations:
Candidate must be a member of CORU.

ISCP membership.

Experience & Skills:
5 years post-graduate experience.

Further qualifications or knowledge in clinical specialist area of spinal injuries and rehabilitation and shoulder injuries.

Demonstrated ability to work within a multi-disciplinary team.

Ability to collaborate with medical staff, performance staff and biomechanists throughout the rehabilitation process to enhance patient care.

Demonstrate clinical reasoning skills to assess issues, develop sound conclusions and recommend an appropriate course of action.

Excellent communication and presentation skills.

Good injury prevention and treatment knowledge with a strong understanding of strength and conditioning principles.

Ability to critique and summarise research in relation to spinal injuries and rehabilitation.

Desirable Knowledge:
Experience working with and delivering services to sporting organisations.

Proficient in the use of testing equipment for spinal rehabilitation.

Equal Opportunity Statement and Benefits

UPMC is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

At UPMC we provide a total rewards program that is not only market competitive, but fair and provides growth opportunities for all our colleagues.

Compensation
- Competitive pay for the work employees do - base pay, performance related pay and premium pay where applicable.

Benefits
- Fully paid maternity and paternity leave for new parents. Competitive Pension Plan. Critical Illness cover for all employees up to the age of 66.

Performance and Recognition
- Rewards for performance that supports the goals and mission of UPMC through our annual ACES programme.

Work-Life Balance
- Flexible working opportunities to support you to work around external family commitments.

Development and Career Opportunities
- Opportunities for each employee to reach their career goals through continued learning and/or advancement.

About UPMC

UPMC is a renowned multinational academic medical centre committed to delivering people-focused care that's close to home. Headquartered in Pittsburgh and affiliated with the University of Pittsburgh Schools of the Health Sciences, UPMC shapes the future of health through clinical and technological innovation, research and education. UPMC expands its expertise globally, bringing world-class care across continents through its UPMC International division - an owned and operated network of hospitals and ambulatory care centres in Italy, Ireland and Croatia. UPMC International brings new access to the signature specialty services of UPMC Hillman Cancer Centre, UPMC Sports Medicine and others to more people in more places around the world.

In Ireland UPMC has provided high-quality healthcare in the South East since 2006. UPMC's operations in Ireland now include UPMC Whitfield Hospital in Waterford, UPMC Sports Surgery Clinic in Dublin, UPMC Kildare Hospital in Clane, and UPMC Aut Even Hospital in Kilkenny. Outpatient care is available at the UPMC Carlow Outreach Centre, UPMC Hillman Cancer Centre radiotherapy locations in Waterford and Cork, UPMC The 4th Practice in Mallow, and across UPMC Sports Medicine Clinics in Dublin, Waterford, Limerick, Tipperary, Cork, and Mayo. UPMC has also established a nationwide Concussion Network. UPMC's Global Technology Operation Centre is based in Kilkenny.

Location: SSC Sports Medicine

Job type: Fixed Term

Overview Of Role
The Clinical Specialist position offers a unique opportunity to provide clinical leadership and expertise within an interdisciplinary team of specialists. It is focussed on spinal MSK conditions. The role involves assessing and treating injuries, designing and implementing rehabilitation pathways and collaborating with the team to enhance the management of spinal conditions. This position is offered on a temporary basis to cover maternity leave.

Clinical Leadership
Primary Duties and Responsibilities:
Lead the spinal rehabilitation service, providing expert consultation and joint working with staff to manage patient care through the rehabilitation pathway.

Lead spinal rehabilitation pathway caseload, assessments and delegate referrals appropriately.

Ensure high standards of patient care by implementing evidence-based practices aligned with national and specialist clinical guidance.

Keep staff informed of recent developments through participation in research-based conferences, network meetings, and postgraduate education and training.

Lead team meetings to inform, engage, and motivate team members and to keep staff updated on hospital policies and strategies.

Lead through innovative practice and continuous development of clinical knowledge and skills.

Rehabilitation
Develop and enhance local pathways of care specifically tailored for spinal rehabilitation patients.

Conduct advanced assessments using investigative and clinical reasoning skills to develop individualised treatment plans.

Evaluate and implement clinical outcome measures to monitor effectiveness of rehabilitation pathways

Management
Manage and organise your patient caseload and support other therapists with complex spinal rehabilitation cases.

Develop and monitor clinical standards for spinal rehabilitation in accordance with local and national guidelines.

Continuously evaluate and improve the effectiveness of the service through service evaluations and clinical audits in collaboration with the Head of Rehabilitation and relevant stakeholders

Responsible for time management and scheduling of CPD for spinal rehabilitation team members.

Staff Development
Support and facilitate continuous professional development for team members.

Maintain high clinical standards and support staff through comprehensive in-service training, one-to-one coaching, clinical supervision, and practical sessions.

Promote personal and professional development through regular staff appraisals, and performance reviews.

Participate actively in postgraduate education and organise specialist courses, liaising with local Universities.

Research & Development
Undertake and support research projects to enhance the evidence base and enhance patient care and service development for the management of spinal rehabilitation.

Communication
Use advanced communication skills to effectively interact with patients and referrers, ensuring understanding and maximising rehabilitation potential.

Ensure confidentiality in all communications, especially regarding patient, carer, and staff information.

Facilitate clear communication within the multi-professional team to coordinate patient care effectively.

Ensure appropriate record keeping and maintenance of good practice in data recording.

Qualifications & Experience
Bachelor of Science (Hons) Degree or equivalent

MSc Physiotherapy, Strength and Conditioning, Sports Science

Registrations
Candidate must be a member of CORU.

ISCP membership.

Experience & Skills
5 years post-graduate experience.

Further qualifications or knowledge in clinical specialist area of spinal injuries and rehabilitation and shoulder injuries.

Demonstrated ability to work within a multi-disciplinary team.

Ability to collaborate with medical staff, performance staff and biomechanists throughout the rehabilitation process to enhance patient care.

Demonstrate clinical reasoning skills to assess issues, develop sound conclusions and recommend an appropriate course of action.

Excellent communication and presentation skills.

Good injury prevention and treatment knowledge with a strong understanding of strength and conditioning principles.

Ability to critique and summarise research in relation to spinal injuries and rehabilitation.

Desirable Knowledge
Experience working with and delivering services to sporting organisations.

Proficient in the use of testing equipment for spinal rehabilitation.

Equal Opportunity Statement And Benefits
UPMC is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
At UPMC we provide a total rewards program that is not only market competitive, but fair and provides growth opportunities for all our colleagues.

Compensation
– Competitive pay for the work employees do – base pay, performance related pay and premium pay where applicable.

Benefits
– Fully paid maternity and paternity leave for new parents. Competitive Pension Plan. Critical Illness cover for all employees up to the age of 66.

Performance and Recognition
– Rewards for performance that supports the goals and mission of UPMC through our annual ACES programme.

Work-Life Balance
- Flexible working opportunities to support you to work around external family commitments.

Development and Career Opportunities
– Opportunities for each employee to reach their career goals through continued learning and/or advancement.

About UPMC
UPMC is a renowned multinational academic medical centre committed to delivering people-focused care that's close to home. Headquartered in Pittsburgh and affiliated with the University of Pittsburgh Schools of the Health Sciences, UPMC shapes the future of health through clinical and technological innovation, research and education. UPMC expands its expertise globally, bringing world-class care across continents through its UPMC International division — an owned and operated network of hospitals and ambulatory care centres in Italy, Ireland and Croatia. UPMC International brings new access to the signature specialty services of UPMC Hillman Cancer Centre, UPMC Sports Medicine and others to more people in more places around the world.

In Ireland UPMC has provided high-quality healthcare in the South East since 2006. UPMC's operations in Ireland now include UPMC Whitfield Hospital in Waterford, UPMC Sports Surgery Clinic in Dublin, UPMC Kildare Hospital in Clane, and UPMC Aut Even Hospital in Kilkenny. Outpatient care is available at the UPMC Carlow Outreach Centre, UPMC Hillman Cancer Centre radiotherapy locations in Waterford and Cork, UPMC The 4th Practice in Mallow, and across UPMC Sports Medicine Clinics in Dublin, Waterford, Limerick, Tipperary, Cork, and Mayo. UPMC has also established a nationwide Concussion Network. UPMC's Global Technology Operation Centre is based in Kilkenny.

About us: St James's Hospital is Ireland's largest acute academic teaching hospital and is based in Dublin's south inner city. Our fundamental purpose is the delivery of health treatment, care and diagnosis as well as health promotion and preventative services at local, regional and national levels. Our academic partner is Trinity College Dublin.

Purpose of the role: The role of the Clinical Specialist Physiotherapist in the Regional Specialist Memory Clinic (RSMC) is to provide a high-quality physiotherapy service to service users of RSMC.

Clinical Specialist Physiotherapist will provide the advanced clinical knowledge and expertise to design and deliver a high-quality service to service users of the Regional Specialist Memory Clinic (RSMC) at St. James's Hospital.

The RSMC will provide a specialised service for patients with complex or uncertain presentations of dementia, under the clinical governance of the Consultant Geriatrician. The Clinical Specialist Physiotherapist will be a member of a multidisciplinary team. The post holder will also provide sessions to the FASU-falls and Syncope unit and accept referrals from the young onset dementia service.

Please review the associated Role Profile for a detailed description of the role, as well as a full list of all eligibility criteria, qualifications and / or experience required.

Also, please view our Online Application information guide, to help guide you through the application form if needed.

For informal enquiries: Please contact Avril Fahey, Physiotherapy Manager-in-Charge III; Ext: 2486; Email: OR Ms Sheila Roche / Mr Tom Meredith, Deputy Physiotherapy Managers, / ,

A panel may be formed from which future vacancies will be filled.

St. James's Hospital is an Equal Opportunities Employer.

Please note: All application forms / CV's (where applicable) must be completed and submitted in English