Find Patient safety manager Jobs in Dublin, D

Clinical Trials Manager (12-month contract)
Zymeworks Inc. —Swords, County Dublin
- Hybrid work
- Bachelor's degree
- Organisational skills
- Communication skills
- Annual leave
Quick apply
6d
Grade VII Quality Patient Safety and Risk Manager SCH0502026
Health Service Executive —South Dublin, County Dublin
10h
Quality Systems & Compliance Manager
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Engineering
- Project management
- Bachelor's degree
13d
Clinic Manager South Anne Street, Ranelagh and Terenure
Sisu Aesthetic Clinic —Dublin, County Dublin
- €35,000–€40,000 a year
- Full-time
- Customer service
- Clinic
- Retail management
- Store discount
- Employee discount
Quick apply
4d
Senior Manager, Process Validation
West Pharmaceutical Services —Dublin, County Dublin
- €100,900–€130,200 a year
- Computer Science
- No degree
- Manufacturing
PM2 Manufacturing Manager (Days)
Amgen —Dún Laoghaire, County Dublin
- €78,613.10–€106,358.90 a year
- Engineering
- English
- Bachelor's degree
11d
Laboratory Aide Histology (Fixed term)
Eurofins Ireland Clinical Diagnostics —DUBLIN 18, County Dublin
- Full-time
- Leaving certificate
- No degree
- Employee assistance program
- Sick pay
Quick apply
6d
Microbiology and Sterility Assurance Lead
Baxter —Dublin, County Dublin
- Management
- Clinic
- Continuous improvement
- Annual leave
Night Nursing Administrator
Irish Cancer Society —DUBLIN 4, County Dublin
- €15,750 a year
- Part-time
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Data entry
- Annual leave
- Employee assistance program
Quick apply
6d
Supply Planner ( 12 Months Fixed Term Contract )
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Excel
- Microsoft Office
- Analysis skills
Peer Support Worker
Bloomfield Hospital —Dublin, County Dublin
- €34,371–€43,914 a year
- Full-time
- No degree
- In-person
Quick apply
12d
Senior Quality Engineer - Validation
West Pharmaceutical Services —Dublin, County Dublin
- €65,208–€82,992 a year
- Engineering
- Manufacturing
- Communication skills
13d
Human Resources Administrator
Blackrock Health Hermitage Clinic —Lucan, County Dublin
- Full-time
- Microsoft Excel
- Administrative experience
- Clinic
- Annual leave
Quick apply
Senior Specialist, Commercial Stability
AstraZeneca —Dublin, County Dublin
- Microsoft Excel
- Microsoft Office
- Presentation skills
8d
Clinical Nurse Manager 2 - Cardiac Catheterisation Labs
Blackrock Health Blackrock Clinic —Dublin, County Dublin
- Full-time
- Research
- Clinic
- Communication skills
- Employee assistance program
Quick apply
5d
Project Engineer
West Pharmaceutical Services —Dublin, County Dublin
- €51,040–€64,960 a year
- Overtime
- Engineering
- Microsoft Office
- Project management
Cancer Nurse
Irish Cancer Society —DUBLIN 8, County Dublin
- €56,600 a year
- Weekend availability
- Nursing
- Leadership
- Communication skills
- Annual leave
- Employee assistance program
Quick apply
8d
Health Care Assistant - Theatre
Beacon Hospital —Dublin, County Dublin
- Full-time
- Nursing
- Clinic
- No degree
Quick apply
Clinical Lead (Ceannaire Cliniciúil) National Gender Healthcare Programme
RCPI —DUBLIN 2, County Dublin
- Monday to Friday
- Leadership
- Annual leave
Quick apply
6d
Senior CT Radiographer
Blackrock Health Hermitage Clinic —Lucan, County Dublin
- Full-time
- Clinic
- Bachelor's degree
- Communication skills
- Free parking
- Employee assistance program
Quick apply
12d

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Clinical Trials Manager (12-month contract)

Zymeworks Inc. -
Swords, County Dublin

Quick apply

Job details

Fixed term
6 days ago

Benefits

Annual leave

Qualifications

Vendor management
Bachelor's degree
Organisational skills
Communication skills

Full job description

Company Description
Zymeworks is a global biotechnology company managing a portfolio of licensed healthcare assets and developing a diverse pipeline of novel, multifunctional biotherapeutics to improve the standard of care for difficult-to-treat diseases, including cancer, inflammation, and autoimmune disease. The Company’s asset and royalty aggregation strategy focuses on optimizing positive future cash flows from an emerging portfolio of licensed products such as Ziihera® (zanidatamab-hrii) and other licensed products and product candidates such as pasritamig. In addition, Zymeworks is also building a portfolio of healthcare assets that can generate strong cash flows, while supporting the early-stage development of innovative medicines. We are a global company headquartered in Vancouver BC, with operations in Bellevue WA, Dublin IRE, and Singapore.

Why Work With Us

Nothing is more critical to our success than the quality of our team. The work we do is meaningful and impactful - we care about each other as well as the patients we serve. We offer challenging career opportunities, competitive benefits and an environment that recognizes and rewards performance.

This role will be located in either Vancouver, BC OR Bellevue, WA OR Dublin, IRE OR New York, US and is hybrid with a minimum of 3 days per week onsite. This is a 12-month fixed term position.

What You'll Do

Clinical Trial Management:

Acts as clinical trial lead on one or two early-phase clinical studies
Maintains global study timelines and aligns study start-up, enrollment, study conduct and close out activities with corporate goals.
Identifies and ensures compliance with Key Performance Indicator (KPI); Key Risk indicators (KRI); and Key quality indicators (KQI) for assigned clinical trial.
Ensures study is carried out according to the study protocol, SOPs, CFR, ICH/GCP guidelines and study-specific manuals and procedures; collaborates with QA to ensure inspection readiness.
Develops and implements study specific processes and trains study teams.
Works closely with the study management team to develop clinical trial protocols and designs all associated clinical forms, including Case Report Forms, SAE Forms, etc. for assigned clinical trial.
Prepares, reviews, and approves study-related documents (e.g., Monitoring plans, Laboratory Manual, Patient Diary and CRF completion guidelines).
Proactively identifies study issues/risks and recommends/implements solutions for assigned clinical trial.
Reviews and analyzes clinical trial data routinely to identify, develop and implement changes required for improvement and compliance at site level and/or study level.
Develops and reviews site budgets working closely with finance and CRO partner.
Plans and conducts, investigator meetings, internal team meetings, and other trial-specific meetings.
Assists in the preparation and follow-up of in-house and on-site quality audits, as well as regulatory authority inspections.

Vendor and Site Management:

Collaborates with CRO to manage site related interactions and serves as a liaison and resource for investigational sites. Troubleshoots and helps to address recruitment obstacles.
Reviews CRO/vendor invoices for accuracy.
Reviews and analyzes the initial and revised scope of service agreements, budgets, plans, and detailed timelines ensuring that performance expectations (timeline/quality/cost) are met with the CRO/vendor.

Clinical Trials Leadership:

Manages assigned clinical trial with minimal oversight.
Participates in the selection, training, and evaluation of study personnel (contract and internal) to ensure the efficient operation of the function.
Develops and implements processes with efficiencies for assigned clinical study
Fosters effective and collaborative working relationships with fellow employees, management, and external partners.
Other related duties as required.

What You'll Bring

University degree and relevant clinical trials experience in pharmaceutical, biotech or CRO setting including clinical trial management experience.
Minimum of 5 years’ pharmaceutical industry drug safety experience, optimally in a small-to-mid cap biotech environment.
An equivalent combination of education and experience may be considered.
Prior experience in lead role of global clinical trials is required.
CRO/vendor management and oversight experience are required.
Oncology clinical research experience is preferred.
Knowledge of and experience with international regulatory adverse event reporting requirements.
Demonstrated line management experience.
Proven interpersonal skills with the ability to work collaboratively as a member of a cross-functional team.
Excellent communication and organizational skills and the ability to work effectively in a high paced, fast changing environment.
Thorough knowledge of FDA/EMA, CFR and GCP/ICH requirements.
Ability to work independently, establish functional priorities and execute on goals.
Experience in oncology drug development desirable.
Ability to travel for site co-monitoring activities, vendor visits/audits as required (up to 30%).

Total Rewards

We offer a comprehensive total rewards package, which includes competitive salaries, generous benefits, an outstanding work environment, and excellent opportunities for professional growth. We regularly benchmark our compensation against leading biotechnology companies in our geographies.

The base salary range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position in the location for which the job is posted and does not include bonus, equity, or benefits. Within the range, individual pay is determined by a variety of factors and the salary offered may vary depending on the successful candidate’s location and qualifications (including, but not limited to, job-related knowledge, education, training, skills, and experience).

Our total rewards package that includes:

Exceptional medical, dental and vision benefits by country
Industry leading vacation and paid time off

This role is not eligible for relocation or immigration support.

All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin or disability.

NOTE TO AGENCIES: Zymeworks values our relationships with our recruiting partners. We only accept resumes from those partners who have been contracted with us. Zymeworks is not responsible for any fees related to resumes that are unsolicited or are received without contract.

The pay range for this role is:
91,500 - 140,300 CAD per year(CA)
116,250 - 178,250 USD per year(US)
66,000 - 101,200 EUR per year(IE)

Quick apply

Refine Your Search

patient safety manager jobs in dublin, d

Clinical Trials Manager (12-month contract)

Grade VII Quality Patient Safety and Risk Manager SCH0502026

Quality Systems & Compliance Manager

Clinic Manager South Anne Street, Ranelagh and Terenure

Senior Manager, Process Validation

PM2 Manufacturing Manager (Days)

Laboratory Aide Histology (Fixed term)

Microbiology and Sterility Assurance Lead

Night Nursing Administrator

Supply Planner ( 12 Months Fixed Term Contract )

Peer Support Worker

Senior Quality Engineer - Validation

Human Resources Administrator

Senior Specialist, Commercial Stability

Clinical Nurse Manager 2 - Cardiac Catheterisation Labs

Project Engineer

Cancer Nurse

Health Care Assistant - Theatre

Clinical Lead (Ceannaire Cliniciúil) National Gender Healthcare Programme

Senior CT Radiographer

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