Find Clinical trial manager Jobs in Dublin County Dublin

Clinical Trials Associate (12-month contract)
Zymeworks Inc. —Swords, County Dublin
- €31,500–€48,300 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Bachelor's degree
- Annual leave
Quick apply
Clinical Trials Associate
Zymeworks Inc. —Swords, County Dublin
- €31,500–€48,300 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Bachelor's degree
- Annual leave
Quick apply
Clinical Trials Manager (12-month contract)
Zymeworks Inc. —Swords, County Dublin
- Full-time
- Hybrid work
- Bachelor's degree
- Organisational skills
- Communication skills
- Annual leave
Quick apply
Clinical Document Management Learning Manager
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Hybrid work
- Research
- Bachelor's degree
- No degree
Senior Clinical Editor
IQVIA —Dublin, County Dublin
- Doctoral degree
- English
- Research
Clinical Data Management Lead, home-based
IQVIA —Dublin, County Dublin
- Remote
- Customer service
- Project management
- Bachelor's degree
Clinical Document Migrations Manager
Novartis —Dublin, County Dublin
- €55,370–€102,830 a year
- Full-time
- Hybrid work
- Agile
- Communication skills
Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead
IQVIA —Dublin, County Dublin
- English
- Microsoft Office
- Bachelor's degree
1d
Research Support Coordinator
Irish Cancer Society —DUBLIN 4, County Dublin
- €37,000 a year
- Full-time
- Hybrid work
- Microsoft Word
- Word processing
- Research
- Annual leave
- Employee assistance program
Quick apply
8d
Senior Clinical Engagement Project Manager
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Project management
- Presentation skills
- Bachelor's degree
- Gym membership
- Life insurance
Quick apply
Senior Manager CSCQ, Qualified Person
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- Bachelor's degree
- In-person
- Annual leave
9d
Funded PhD
National Institute for Bioprocessing Research and Training (NIBRT) —Dublin, County Dublin
- €25,000 a year
- Doctoral degree
- Engineering
- Research
Clinical Engagement Project Manager
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Hotel
- Project management
- Presentation skills
- Gym membership
- Life insurance
Quick apply
Operations Manager - Dublin
Re:Cognition Health —DUBLIN 24, County Dublin
- €50,000 a year
- Full-time
- Clinic
- Communication skills
- Annual leave
- Employee assistance program
Quick apply
9d
Associate Director Inspection Management (GCP)
Regeneron —Dublin, County Dublin
- €101,500–€165,200 a year
- Management
- Supervising experience
- Presentation skills
- Annual leave
GMDP Quality Assurance Manager
WEP Clinical —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)
IQVIA —Dublin, County Dublin
- Remote
- Project management
- Recruiting
- Communication skills
5d
Senior Clinical Data Analyst
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Excel
- Data analysis skills
- Master's degree
- Gym membership
- Life insurance
Quick apply
Vendor Startup Manager IRT – Single Sponsor (home-based)
IQVIA —Dublin, County Dublin
- Remote
- Continuous improvement
- Budgeting
- Communication skills
Programme Lead
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Hotel
- Project management
- No degree
- Gym membership
- Life insurance
Quick apply

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Clinical Trials Associate (12-month contract)

Zymeworks Inc.
Swords, County Dublin

Quick apply

Job details

Full-time
€31,500–€48,300 a year

Benefits

Annual leave

Qualifications

Biology
Microsoft Excel
Microsoft Office
Bachelor's degree
Organisational skills
SharePoint
Chemistry
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 Dublin, IRE OR Bellevue, WA and is hybrid with a minimum of 3 days per week onsite. This is a 12-month fixed term position.

What You'll Do

Provide administrative support to clinical trial teams.
Assist in the preparation and maintenance of essential trial documents.
Organize internal study team meetings and issue agendas/minutes (with approval from CTM).
Assist and support eTMF Manager in QC of eTMF.
Set up and ensure all study-related documents are filed per folder structure on internal filing repository (Sharepoint).
Assist CTM in keeping internal study conduct tracker, and any other oversight trackers up-to-date.
Maintain study conduct metrics, including but not limited to study start up timelines, enrollment rates, screen-failure rates and deviation rates.
Monitoring review oversight of external vendor.
Patient data review in collaboration with cross-functional teams and external vendor.
Assist in reviewing invoices, including pass-throughs, referring to site agreements, patient enrollment and/or monitoring visit trackers.
Carry out the function of the role in compliance with company Standard Operating Procedures (SOPs), working practices and regulatory guidelines.
Foster effective and collaborative working relationships with cross-functional teams and management globally to ensure trial milestones are met.
Promote timely and accurate communication amongst the internal and external teams.
Serves as back-up to the CTM, when needed.

What You'll Bring

Bachelor’s degree preferably in the field of biology, chemistry or health sciences and 1-3 years’ previous clinical research experience.
Prior Clinical Trials Associate experience in oncology preferred.
Proven interpersonal skills with the ability to work collaboratively as a member of cross-functional and global team. Ability to establish and maintain effective working relationships.
Good organizational skills and the ability to work effectively in a high paced, fast changing, compliance-driven environment. Results-oriented and flexible attitude.
Ability to track and manage key dates/deadlines.
Basic knowledge of drug development and FDA GCP regulatory guidelines.
Familiarity with FDA/ICH regulatory requirements for clinical trials is desired.
Excellent oral and written communication skills, with particular attention to detail.
Ability to appropriately handle confidential information.
Proficiency with MS Office and Excel.

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:

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

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:
31,500 - 48,300 EUR per year(IE)
56,250 - 86,250 USD per year(US)

Quick apply

Refine Your Search

clinical trial manager jobs in dublin county dublin

Clinical Trials Associate (12-month contract)

Clinical Trials Associate

Clinical Trials Manager (12-month contract)

Clinical Document Management Learning Manager

Senior Clinical Editor

Clinical Data Management Lead, home-based

Clinical Document Migrations Manager

Assoc Director, Quality Management - Client Dedicated Clinical Compliance Optimization Lead

Research Support Coordinator

Senior Clinical Engagement Project Manager

Senior Manager CSCQ, Qualified Person

Funded PhD

Clinical Engagement Project Manager

Operations Manager - Dublin

Associate Director Inspection Management (GCP)

GMDP Quality Assurance Manager

Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)

Senior Clinical Data Analyst

Vendor Startup Manager IRT – Single Sponsor (home-based)

Programme Lead

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