Senior Statistical Analyst Reading

Meeveem Limited; Reading; On-site; GBP 40,000 - 65,000; Full time

Benefits offered by this job

Competitive base salary and performance-related incentives

Health and wellbeing programs

Retirement and pension plans

Learning and development opportunities

Job summary

Meeveem Limited is seeking a Senior Statistical Analyst to enhance the design and analysis of clinical trials. You will play a key role in statistical methodologies and collaborate across teams while contributing to innovative treatments.

The ideal candidate will hold a Master’s or Ph.D. in a relevant field and have at least 5 years of experience, proficient in software like SAS, R, or Python. The position includes a competitive salary and comprehensive benefits package that supports health and career development.

Qualifications

• Minimum of 5 years of experience in statistical analysis within the pharmaceutical, biotechnology, or CRO industry.
• Strong understanding of clinical trial design and regulatory requirements.
• Excellent analytical and communication skills.

Responsibilities

• Collaborate with cross-functional teams to design statistical methodologies for clinical trials.
• Conduct statistical analyses and interpret results to support decision-making.
• Develop and validate statistical models to analyze clinical trial data.

Skills

Statistical analysis

Clinical trial design

Data interpretation

Statistical software (SAS, R, Python)

Education

Master's or Ph.D. in Statistics, Biostatistics, or related field

Job description

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values‑driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. We are currently seeking a Senior Statistical Analyst to join our diverse and dynamic team. As a Senior Statistical Analyst at ICON, you will play a pivotal role in designing and analyzing clinical trials and contributing to the advancement of innovative treatments and therapies.

What you will be doing

• Collaborating with cross‑functional teams to design statistical methodologies and analysis plans for clinical trials.
• Conducting statistical analyses and interpreting results to support decision‑making and regulatory submissions.
• Developing and validating statistical models to analyze clinical trial data and evaluate treatment outcomes.
• Providing statistical expertise and guidance to support study design, protocol development, and data interpretation.
• Contributing to the development of statistical analysis protocols and programming specifications.

Your profile

• Master's or Ph.D. degree in Statistics, Biostatistics, or a related field.
• Minimum of 5 years of experience in statistical analysis within the pharmaceutical, biotechnology, or CRO industry.
• Proficiency in statistical software such as SAS, R, or Python.
• Strong understanding of clinical trial design, statistical methodologies, and regulatory requirements.
• Excellent analytical, problem‑solving, and communication skills.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please submit a request through our careers site.