Find clinical trials Jobs in dublin, d

Associate Director, Statistical Programming
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Doctoral degree
- Computer Science
- Master's degree
Business Support Specialist 12 month Fixed Term Contract
AllPhar Services Limited —DUBLIN 24, County Dublin
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Analysis skills
Quick apply
FICO Business Analyst
Uniphar PLC —DUBLIN 24, County Dublin
- Full-time
- Communication skills
Quick apply
Senior AI Platform Engineer
Signant Health —Dublin, County Dublin
- Full-time
- Computer Science
- Salesforce
- Master's degree
Director and Head of EMEA Emerging Biopharma Sales, IQVIA Central Laboratories
IQVIA —Dublin, County Dublin
- Full-time
- Analysis skills
- Communication skills
- Negotiation
Associate Biostatistics Director - FSP (Permanent Home-based)
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- Doctoral degree
- Leadership
- Communication skills
Associate Director, Biostatistics
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Doctoral degree
- English
- Master's degree
Service Delivery Director
Uniphar PLC —DUBLIN 24, County Dublin
- Full-time
- Azure
- Computer Science
- Analysis skills
Quick apply
13d
DevOps Engineer
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Computer Science
- DevOps
- Engineering
- Gym membership
- Life insurance
Quick apply
Mid-Level Backend Software Engineer
Teckro Limited —Dublin, County Dublin
- Full-time
- Hybrid work
- Computer Science
- System design
- Hotel
- Gym membership
- Life insurance
Quick apply
Senior Enterprise Account Manager, AGS Ireland/NI (Cross Industries)
Amazon Web Services EMEA SARL (Irish Branch) —Dublin, County Dublin
- Full-time
- Sales
- AWS
- Negotiation
2d
ServiceNow Architect
Uniphar PLC —DUBLIN 24, County Dublin
- Full-time
- JavaScript
- Scripting
- Communication skills
Quick apply

More jobs to discover

Find similar jobs that you might be interested in.

Business Support Specialist 12 month Fixed Term Contract
AllPhar Services Limited —DUBLIN 24, County Dublin
The company’s main divisions encompass everything from International Sales through Sales to NGO’s and Charities, Clinical Trials Supply, Imported (Unlicensed…
Quick apply
HR Professional - Fixed term contract
Brown Brothers Harriman —Dublin, County Dublin
Bachelors degree or equivalent work experience; CIPD member preferred. A minimum of 2 years relevant Human Resources experience; preferably in the financial…
20h

I want to receive the latest job alerts for clinical trials in dublin, d

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical trials jobs near dublin, d

Head Of Sales jobs in Dublin, County Dublin

Platform Engineer jobs in Dublin, County Dublin

Associate Director jobs in Dublin, County Dublin

Devops Engineer jobs in Dublin, County Dublin

Business Analyst jobs in Limerick, County Limerick

Business Analyst jobs in Trinity College, County Dublin

Business Analyst jobs in Galway, County Galway

Business Analyst jobs in Cork, County Cork

Business Development jobs in County Galway

Greenogue Business Park jobs in Dublin, County Dublin

Remote Data Analyst jobs in Dublin, County Dublin

Business Analyst jobs in Tralee, County Kerry

Sales jobs in Dublin, County Dublin

Head Of Sales jobs in County Dublin

Head Of Sales jobs in Remote

Head Of Sales jobs in Galway, County Galway

Bathroom Sales jobs in Dublin, County Dublin

Sales Assistant jobs in County Galway

Sales Advisor jobs in Dublin, County Dublin

Senior Qa Engineer jobs in Dublin, County Dublin

Associate Director, Statistical Programming

Grifols Worldwide Op Ltd -
Dublin, County Dublin

Apply Now

Job details

Full-time

Benefits

Private medical insurance

Qualifications

Doctoral degree
Computer Science
SAS
R
Master's degree
Bachelor's degree
Organisational skills
Leadership
Communication skills
Python

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:

The Associate Director provides Statistical Programming leadership and expertise in support of clinical development and post‐marketing activities for multiple therapeutic areas. Participates in the development, registration, and life cycle management of Grifols products.

Drives standardization within the Biometry group, innovating to develop processes/systems/tools designed to improve automation and efficiency of all aspects of reporting of clinical trials – including standard checking of deliverables generated by Contract Research Organizations (CROs).

Contributes strategically to project decisions with a focus on pre-study planning, reporting and submission preparation within and across projects.

What you'll do

The duties and responsibilities include, but are not limited to, the following:

Provides specific functional expertise, leadership and strategic thinking within Biometry.
Responsible for ensuring overall quality of analysis and reporting deliverables for global Phase I‐IV clinical trials and research publication efforts.
Acts as a lead programmer, generating/validating CDISC compliant statistical analysis database and outputs (i.e., tables, listings, figures, and inferential statistical output) using SAS, R or other software.
Leads the development and adaptation of new Statistical Programming tools/processes in support of Grifols drug development.
Responsible for establishing and maintaining policies, standards and guidance for Statistical Programming operations in adherence with ICH and regulatory requirements.
Oversees projects which relate to improving processes and quality and efficiency of clinical reporting within the Biometry group.
Determines efficient utilization of Statistical Programming resource by leveraging both in‐house staff and external vendors. Provides input on optimal resource utilization and capacity.
Manages outside CROs and consultants within the programming function, as needed. Maintains constant and open communication to make sure timely and quality deliverables and support CRO selection processes.
Drives the development of tools for continual assessment of CRO contributions to clinical trials.
Provides support in the development of programmers within the Statistical Programming and Data Management groups.
Provides Statistical Programming consultancy to colleagues, leveraging project management, technical leadership abilities and submission requirements knowledge, with a hands-on and collaborative approach.
Contributes to the hiring and mentoring of statistical programmers within the Biometry group.

What you'll bring

Expert knowledge of SAS, R or Python.
High degree of expertise in CDISC and other industry standards, tools and regulatory requirements.
Demonstrate a high degree of independence, technical skills, with the ability to influence the team, internal stakeholders and external vendors to achieve results with minimal to no supervision.
Ability and experience to determine overall programming strategy for the Biometry group.
Demonstrate strong problem solving and risk‐mitigation skills. Is a strategic and creative thinker.
Excellent interpersonal, verbal and written communication skills.
Strong attention to detail and excellent organizational skills.
Comfortable working in a dynamic, fast-paced environment.
Qualifications and Experience
Bachelors’ degree or higher in computer science, bioinformatics, biostatistics or related field.
Requires a PhD with a minimum of 10 years of clinical development experience in the pharmaceutical/biotech industry or an MSc with a minimum of 12 years’ experience or a BSc with a minimum of 15 years’ experience.

Our Benefits Include:

Highly competitive salary
Group pension scheme - Contribution rates are 5% employer and 5% employee
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 trials jobs in dublin, d

Associate Director, Statistical Programming

Business Support Specialist 12 month Fixed Term Contract

FICO Business Analyst

Senior AI Platform Engineer

Director and Head of EMEA Emerging Biopharma Sales, IQVIA Central Laboratories

Associate Biostatistics Director - FSP (Permanent Home-based)

Associate Director, Biostatistics

Service Delivery Director

DevOps Engineer

Mid-Level Backend Software Engineer

Senior Enterprise Account Manager, AGS Ireland/NI (Cross Industries)

ServiceNow Architect

More jobs to discover

I want to receive the latest job alerts for clinical trials in dublin, d

Related Searches

Explore jobs in more locations

Jobseeker tools

Employer Tools

Browse

Stay Connected