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Parexel

End-to-end clinical trials and regulatory consulting

Health Economics Associate

ConsultingConfirmed live in the last 24 hours
Full-timeHyderabad, Telangana, IndiaNo salary listedRemote

About the Job

Requirements

  • A Master's degree or equivalent in a life science or quantitative discipline such as health economics, economics, mathematics, statistics, or a related field.
  • Strong communication, organization, and problem-solving skills.
  • Advanced proficiency in Microsoft Office applications, particularly Excel.
  • High analytical ability and strong written accuracy.

Responsibilities

  • Perform comprehensive data analysis to support health economic model development and validation.
  • Assist in building and adapting health economic models for country-specific applications and reimbursement requirements.
  • Conduct systematic searches for published health economic models and Health Technology Assessment body guidance to inform model development.
  • Check and validate health economic models using appropriate software tools to ensure accuracy and elucidate the economic value of clients' products.
  • Support senior team members in project execution, including model documentation, quality assurance, and deliverable preparation.
  • Collaborate with cross-functional teams to understand client needs and translate requirements into model specifications.
  • Maintain high standards of scientific accuracy and attention to detail in all analytical work and documentation.
  • Contribute to the continuous improvement of health economic modeling processes and methodologies.

Desired Qualifications

  • Strong analytical ability and attention to detail in complex quantitative work.
  • Advanced computing skills, particularly in Microsoft Excel with proficiency in macros and VBA.
  • Excellent written and oral communication skills, especially in conveying technical information clearly.
  • Experience working in healthcare, pharmaceutical, or regulated research environments.
  • Self-motivation, enthusiasm, and flexibility in a dynamic project-based setting.
  • Keen interest in medical research, healthcare delivery, and the pharmaceutical industry.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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