Health Economics and Outcomes Research Liaison

Redbock - an NES Fircroft company; United States; Remote; USD 60,000 - 80,000; Full time

Job summary

A leading biotechnology company is seeking a Health Economics and Outcomes Research Liaison for a fully-remote 12-month contract. The role involves supporting launch deliverables for oncology therapies and requires extensive experience in HTA submissions. Candidates should have a strong background in systematic literature reviews and evidence synthesis projects, along with a relevant degree.

Benefits

Medical insurance

Vision insurance

401(k)

Disability insurance

Qualifications

• 5-10 years of industry experience preparing HTA regulatory submissions.
• Strong experience with Evidence Packages: Systematic Literature Review & Indirect Treatment Comparison.
• Hands-on experience managing HEOR evidence synthesis projects.

Responsibilities

• Support launch deliverables related to the JCA submission of adjuvant and advanced melanoma.
• Prepare HTA regulatory submissions and global value dossiers.
• Provide technical support to revise documents.

Skills

Systematic Literature Review

HTA Requirements

Evidence Packages Development

Meta-analysis

Education

MS or BS Degree

Job description

Health Economics and Outcomes Research Liaison

Health Economics and Outcomes Research Liaison

1 day ago Be among the first 25 applicants

Redbock - an NES Fircroft company provided pay range

This range is provided by Redbock - an NES Fircroft company. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$85.00/hr - $100.00/hr

Direct message the job poster from Redbock - an NES Fircroft company

Our client is a leading biotechnology company who is focused on developing and commercializing therapies for cancer, infectious diseases, cardiovascular diseases, and rare diseases. The client needs an HEOR Consultant for 12-months who can support launch deliverables for the JCA submission of oncology therapies.

This is a fully-remote assignment. Occasional travel to the client in NY may be required. Expected workload is 40 hours/week.

Responsibilities:

• Support launch deliverables related to the JCA submission of adjuvant and advanced melanoma (Oncology)
• Preparing HTA regulatory submissions for upcoming JCA submissions and global value dossier experience
• Strong knowledge of systematic literature reviews and HTA requirements
• Knowledge of SOR/ITC experience is a must
• Hands-on technical support to quickly revise documents

Requirements:

• MS or BS Degree minimum, advanced degree is preferred but not required.
• 5-10 years of industry experience preparing HTA regulatory submissions, and global value dossiers.
• Strong experience with the development of Evidence Packages: Systematic Literature Review (SLR) & Indirect Treatment Comparision (ITC)
• Excellent knowledge of pair-wise and network meta-analysis and population adjusted indirect comparisons
• Hands-on experience and ability to design and manage HEOR evidence synthesis projects that fulfill the guidelines (ISPOR) and HTA regulatory submissions (NICE, IQWiG, HAS) (i.e. UK, Germany, France).

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Research and Consulting

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Disability insurance

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