Find Clinical trials associate Jobs in Lucan, D

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 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
Associate Principal/Principal Qualitative Research, Patient Centered Solutions
IQVIA —Dublin, County Dublin
- Full-time
- Hybrid work
- Doctoral degree
- Data analysis skills
- English
Clinical Research Associate II
IQVIA —Dublin, County Dublin
- Full-time
- No degree
- In-person
12d
Associate Director Quality - Client Dedicated ( Regional Clinical Compliance Lead)
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's degree
- Work from home
5d
Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's degree
- Work from home
5d
CNM2; Clinical Trials Research Nurse; Oncology
Beacon Hospital —Dublin, County Dublin
- Full-time
- Management
- Research
- Microsoft Office
- Annual leave
Quick apply
12d
Clinical Quality Assurance - Program Lead (Associate Director)
Novartis —Dublin, County Dublin
- €72,800–€135,200 a year
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
Associate Director, Drug Product Development
Jazz Pharmaceuticals —Dublin, County Dublin
- €157,600–€236,400 a year
- Engineering
- Project management
- Leadership
- Annual leave
Senior Manager, Operations Supply Planner
Bristol-Myers Squibb —Dublin, County Dublin
- Full-time
- Microsoft Excel
- ERP systems
- Analysis skills
Associate Director, Quality Control - Bioassay
MSD —Dunboyne, County Meath
- Full-time
- Doctoral degree
- Engineering
- Master's degree
12d
Senior Director, Planning and Resource Management
ICON Plc —Dublin, County Dublin
- Full-time
- Bachelor's degree
- Leadership
- Communication skills
12d
Trial Vendor Associate Director
Novartis —Dublin, County Dublin
- €75,880–€140,920 a year
- Full-time
- No degree
- Communication skills

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Clinical Trials Associate (12-month contract)
Zymeworks Inc. —Swords, County Dublin
In addition, Zymeworks is also building a portfolio of healthcare assets that can generate strong cash flows, while supporting the early-stage development of…
€31,500–€48,300 a year
Quick apply

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Clinical Trials Associate

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 and is hybrid with a minimum of 3 days per week onsite.

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
Zymelife health and wellness benefits
Matching RRSP / 401K / Pension program
Employee Share Purchase Program
Employee Equity Program
Paid time off to volunteer in your community

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)

Quick apply

Refine Your Search

clinical trials associate jobs in lucan, d

Clinical Trials Associate

Clinical Trials Associate (12-month contract)

Associate Principal/Principal Qualitative Research, Patient Centered Solutions

Clinical Research Associate II

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Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

CNM2; Clinical Trials Research Nurse; Oncology

Clinical Quality Assurance - Program Lead (Associate Director)

Associate Director, Drug Product Development

Senior Manager, Operations Supply Planner

Associate Director, Quality Control - Bioassay

Senior Director, Planning and Resource Management

Trial Vendor Associate Director

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