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Associate Biostatistics Director - FSP (Permanent Home-based)
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- Doctoral degree
- Leadership
- Communication skills
- Work from home
Senior Associate - MLRO
Waystone —Dublin, County Dublin
- Full-time
- Hybrid work
- Presentation skills
- No degree
- Communication skills
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Associate - Corporate Secretarial Services (COE)
Waystone —Dublin, County Dublin
- Full-time
- Hybrid work
- English
- Bachelor's degree
- No degree
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Associate Director, Program & Alliance Management
Zymeworks Inc. —Swords, County Dublin
- €90,000–€138,000 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Communication skills
- Annual leave
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2h

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Senior Associate - MLRO
Waystone —Dublin, County Dublin
An internationally recognized professional third level qualification; Self-starter with clarity of analysis and of expression, both written and oral;
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Associate Biostatistics Director - FSP (Permanent Home-based)

IQVIA -
Dublin, County Dublin

Apply Now

Job details

Full-time

Benefits

Work from home

Qualifications

Doctoral degree
SAS
SAP
R
Predictive analytics
Leadership
Communication skills

Full job description

Dublin, Ireland | Full time | Home-based | R1503450

Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions.
Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews. Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents.
Provide statistical thought partnership for innovative study design and clinical development plans, including Go-No Go criteria and probability of technical success calculations.
Provide for project-wide planning of analyses; quality and timely delivery of interim and final results, including integrated analyses for submissions.
Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA)
Be responsible for interpreting analysis results and ensuring reporting accuracy in study reports and regulatory documents.
Prepare abstracts, posters, oral presentations and written reports to effectively communicate results of clinical programs and studies to internal and external stakeholders and colleagues with varying levels of clinical research knowledge

Education

- PhD or MS in Biostatistics, Statistics or related field

Experience

Minimum of 8 years of experience in clinical trial statistics, preferably within a pharmaceutical or CRO setting.
 Technical Expertise:
Advanced proficiency in SAS / R for data analysis and statistical programming.
Experience with Bayesian methods, predictive modeling, and simulation techniques.
Proven track record in strategic study design, including adaptive designs, sample size calculations, and interim analysis planning.
Familiarity with regulatory guidance on statistical methodologies (e.g., FDA, EMA, PMDA).
Solid experience in applications of advanced statistical methodologies
Leading roles in regulatory submissions
Experience in interactions with major regulatory authorities preferred
Demonstrated statistical expertise and leadership in facilitating and optimizing the (pre/early/full-) clinical development strategy
 Study Design and Strategy:
Ability to lead statistical discussions during protocol development and study planning.
Skilled in defining statistical analysis plans (SAP) and developing strategic approaches for complex study designs.
Experience in strategy discussions involving adaptive design, go/no-go criteria, and futility analyses.
 Collaboration and Communication:
Strong communication skills to effectively present statistical concepts to cross-functional teams.
Proven experience in collaborating with clinical and regulatory teams to align statistical strategy with overall program objectives.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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associate director, linux/unix admin jobs in dublin 2, d

Associate Biostatistics Director - FSP (Permanent Home-based)

Senior Associate - MLRO

Associate - Corporate Secretarial Services (COE)

Associate Director, Program & Alliance Management

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