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Health Economics Associate (Fixed-term contract)

Role overview

Qualifications

  • Master or higher degree in Public Health, Health Economics, Health Policy, Statistics, Biostatistics, Mathematics, or other quantitative fields.
  • Strong basis in fundamental statistical concepts and methods.
  • Familiarity with machine learning techniques and Bayesian statistics is a plus.
  • Strong statistical programming skills with standard software.

Responsibilities

  • Supporting in drafting statistical sections of protocols, performing sample size and power calculation for studies.
  • Contributing to the preparation of specifications for analysis datasets.
  • Developing statistical programs to generate listings, tables and figures as outlined by a statistical analysis plan.
  • Reviewing study protocols and providing input to statistics section.

About the company

Parexel logo

Parexel

Contract Research Organizations (CRO)

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

  • About this role:

  • The Associate contributes statistical capabilities and methodological support at all stages of projects, from planning to completion. The role would work under the supervision on an experienced team member in designing, developing, and delivering client solutions across multiple projects – leveraging competencies in statistical theory, data analysis and interpretation, regression analysis, and experimental design.

  • Knowledge and Experience Required for this role:

    -Familiarity with healthcare consulting or pharmaceutical organizations. Strong basis in fundamental statistical concepts and methods and familiarity with techniques such as development of predictive equations, survival analysis (including parametric methods), longitudinal data analysis, meta-analysis, mixed treatment comparison, and other hierarchical analysis techniques, etc.

    Familiarity with machine learning techniques and Bayesian statistics is a plus.

    Strong statistical programming skills with standard software.

    Education:

    Master or higher degree in Public Health, Health Economics, Health Policy, Statistics, Biostatics, Mathematics, or other quantitative fields.

    Skills:

    Ability to work under pressure to meet multiple and sometimes competing deadlines.

    Excellent scientific, business writing, and presentation skills with close attention to detail.

    Exceptional communication skills, especially in the relaying of technical information and project concepts.

    Competent in written and spoken English SAS, R, SQL, or Python

    Strong communication (spoken and written) and problem-solving skills, and an ability to learn-quickly.

    Ability to communicate effectively, in non-technical terms, with project team members.

    Ability to work well in a team as well as independently and be able to take leadership role with regard to methodological elements in projects.

  • Job Description

    Key Accountabilities:

    Project Execution

    • Acting as support biostatistician or statistical programmer to interact with the study team and the sponsor 

    • Support in drafting statistical sections of protocols, performing sample size and power calculation for studies.

    • Supporting in reviewing data management plans, data specifications, and other related study documents  

    • Supporting in developing statistical analysis plans  

    • Contributing to the preparation of specifications for analysis datasets  

    • Supporting in developing statistical programs to generate listings, tables and figures as outlined by a statistical analysis plan  

    • Performing QC of TLFs and other analysis datasets  

    • Reviewing study protocols and providing input to statistics section  

    • Providing statistical input to Clinical Study Reports 

    • To help ensure quality standards are adhered to on all projects and new methodologies and techniques are adequately assessed and implemented.

    • To help foster thought leadership opportunities.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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