Find clinical trial Jobs in dublin, d

Clinical Trial Associate
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
Risk Surveillance Lead
Novartis —Dublin, County Dublin
- Full-time
- English
- Bachelor's degree
- No degree
Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- Project management
- Recruiting
- Communication skills
Principal Statistician Oncology with Submission Experience
サイネオス・ヘルス —Dublin, County Dublin
- Doctoral degree
- English
- Communication skills
4d
Clinical Engagement Project Manager
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Hotel
- Project management
- Presentation skills
- Gym membership
- Life insurance
Quick apply
Senior Principal Clinical Data Scientist
Novartis —Dublin, County Dublin
- Full-time
- Master's degree
- Mentoring
- Organisational skills
Principal Biostatistician - Biomarker (EMEA Remote)
サイネオス・ヘルス —Dublin, County Dublin
- Doctoral degree
- Master's degree
- No degree
8d
Surgical Business Development Manager
M.E.D Surgical Limited IRL —Dublin, County Dublin
- Full-time
- Business development
Quick apply
Principal Statistical Programmer (PK/PD) (m/w/d)
IQVIA —Dublin, County Dublin
- Full-time
- Communication skills
9d
HR Administrator
Uniphar Wholesale Limited —DUBLIN 24, County Dublin
- Full-time
- Continuous improvement
- Human resources
- Organisational skills
Quick apply
3d
Associate Director, Translational Medicine
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Doctoral degree
- Master's degree
- Project management
Head of Global Regulatory Affairs Strategy
Viatris —Northern Cross, County Dublin
- Full-time
- Doctoral degree
- Master's degree
- Business
9d
Product Support Specialist
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Hotel
- Communication skills
- Time management
- Gym membership
- Life insurance
Quick apply
Principal Biostatistician (R/Rshiny - EMEA BASED)
サイネオス・ヘルス —Dublin, County Dublin
- Doctoral degree
- English
- JavaScript
Neurovascular Postdoctoral Researcher
National Institute for Bioprocessing Research and Training (NIBRT) —Dublin, County Dublin
- Remote
- Doctoral degree
- Research
- Analysis skills
- Annual leave
Neurovascular Research Fellow
National Institute for Bioprocessing Research and Training (NIBRT) —Dublin, County Dublin
- Doctoral degree
- Data analysis skills
- Research
- Annual leave
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
Associate Director, Statistical Programming
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Doctoral degree
- Computer Science
- Master's degree
Associate Biostatistics Director - FSP (Permanent Home-based)
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- Doctoral degree
- Leadership
- Communication skills
Business Development Executive
Cencora —Dublin, County Dublin
- Full-time
- Sales
- Business development
- Communication skills

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Clinical Trial Associate

Grifols Worldwide Op Ltd -
Dublin, County Dublin

Apply Now

Job details

Full-time

Benefits

Private medical insurance

Qualifications

Logistics

Full job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

POSITION SUMMARY:

Provides administrative/clinical support on assigned clinical projects/programs to ensure needs are met within timelines established.

What you'll do:

Assists the clinical team in daily study operations.
Communicates with internal and external customers to increase project and departmental efficiencies
Coordinates the scheduling of internal team meetings, cooperating with the drafted agenda and creating the meeting minutes. May also present during the meetings.
Coordinates logistics of study related meetings including medical expert meetings, investigator meetings, and kick off meetings. Assists in project travel plans, reservations, and expense reports, specific to meetings wherein they were responsible for.
Maintains project related trackers and provides this information to the rest of the study team as needed.
Maintains clinical trial management system (CTMS). Creates studies within the system per standard operating procedures (SOPs), tracks study specific data, and generate reports.
Assists in the preparation, creation and quality review of key clinical study documents such as informed consent documents, essential regulatory document requirements, study manuals, investigator brochures, protocols, clinical study reports and, at start-up, may review and check investigational product (IP) release documents.
Assists in the distribution of key clinical study documents such as investigator brochures, protocols, informed consents, and regulatory submissions.
Follows up on study progress and coordinate updates and/or retrieval of appropriate regulatory documents throughout the study.
Submits and tracks essential documents to the Trial Master File (TMF) on an ongoing basis.
Assists in the archival of clinical research organization (CRO) study files.
Coordinates the set-up, filing, maintenance, and periodic review of TMF and project electronic filing system throughout the study.
Collaborates with other departments and vendors, if needed, on the review and maintenance of the TMF.
Performs the filing, maintenance, and periodic review of project TMF throughout the study in case the task has not been delegated to a vendor.

What you'll bring

Qualifications

Associate’s degree in life science field preferred
2 years of experience as a clinical trial associate

Desireable:

4 years of experience as a clinical trial associate
Relevant experience in clinical research

Our Benefits Include:

Highly competitive salary
Group pension scheme - Contribution rates are (3%/ 5%/ 7%) and company will match
Private Medical Insurance for the employee
Ongoing opportunities for career development in a rapidly expanding work environment
Succession planning and internal promotions
Education allowance
Wellness activities - Social activities eg. Padel, Summer Events

We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you

#LI-FD1

Location: Grange Castle International Business Park, Grange, Co. Dublin, D22 K2R3

Learn more about Grifols

Apply Now

Refine Your Search

clinical trial jobs in dublin, d

Clinical Trial Associate

Risk Surveillance Lead

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

Principal Statistician Oncology with Submission Experience

Clinical Engagement Project Manager

Senior Principal Clinical Data Scientist

Principal Biostatistician - Biomarker (EMEA Remote)

Surgical Business Development Manager

Principal Statistical Programmer (PK/PD) (m/w/d)

HR Administrator

Associate Director, Translational Medicine

Head of Global Regulatory Affairs Strategy

Product Support Specialist

Principal Biostatistician (R/Rshiny - EMEA BASED)

Neurovascular Postdoctoral Researcher

Neurovascular Research Fellow

Senior Clinical Engagement Project Manager

Associate Director, Statistical Programming

Associate Biostatistics Director - FSP (Permanent Home-based)

Business Development Executive

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