Value & Evidence Research Associate

Company : Pioneer Data Systems

Country: United States

Location : New York County, New York

Post: Wed, 31 May 2023 06:31:36 GMT

Expires: Wed, 28 Jun 2023 23:59:59 GMT

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—————————— Job Description ——————————

Position Details:

Our client, a world-leading Pharmaceutical Company in New York, NY is currently looking for a Research Associate / Public Health / HEOR-Observational Studies / HYBRID WORK to join their expanding team.

Job Title: Research Associate / Public Health / HEOR-Observational Studies / HYBRID WORK

Duration: 12 months contract, extendable up to 36 months

Location: New York, NY

Hybrid work: 2 days/week onsite

Note:

The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.

You may participate in the company group medical insurance plan

Job Description:

Value & Evidence Research Associate

Summary:

Client is looking for a Global Value & Evidence (V&E; Health Economics and Outcomes Research) Research Associate (RA) to join our Duchenne muscular dystrophy (DMD) gene therapy (GTx) team within Rare Disease (RD) Global Access and Value (GAV).

The RA will serve as the point-of-contact for budget tracking and compliance-related processes, including those associated with observational studies, as well as support contracting with vendors and health care professionals.

They are also expected to be involved in the development of presentations / reports & publication support.

Finally, the RA will support HEOR-related work, including database analyses using administrative claims or electronic medical records databases, literature review and evidence syntheses, and economic modeling / value dossier development.

This position is full time and based at New York Headquarters (NYHQ).

The RA will report to the V&E Director.

Responsibilities:

Conduct literature reviews to understand the burden of illness and estimate the prevalence & incidence of DMD to inform study design & cross-functional decision-making

Contribute to the development and maintenance of comprehensive global tools such as dossiers (Global Value Dossiers and AMCP dossiers), health economic models, etc. to support optimal pricing and market access

Assist in the planning and conduct of V&E studies (including real world evidence studies) to characterize the burden of disease to support unmet medical needs or to address gaps in clinical and economic value

Facilitate the generation of publications to communicate study findings in scientific channels in the alignment of product publication strategy

Represent GAV at clinical trial team meetings and disseminate key information to V&E colleagues

Prepare reports and presentations to communicate strategic plans, study findings, project deliverables, and general updates to internal and external audiences

Provide support across products and team members in the GAV RD business unit, as well as cross-functional (Medical, Commercial, Corporate Affairs) support and communication as necessary

Manage relationships/coordinates activities such as advisory panels and best practice sharing with users of the program

Execute and manage projects with external collaborators/vendors to ensure timely completion and quality of deliverables as well as budget/legal and Pharmaceutical SOP compliance

Support management of allocated project budgets to align with priorities and spend forecasts, including tracking invoices and updating internal budget system

Oversee team master decks with project summaries and tracking to ensure updates are implemented on a rolling basis

Works with project teams to manage the day-to-day activities of studies.

Qualifications:

Master’s degree or PhD in one of the following is preferred: epidemiology, health services research, public health, health economics, or equivalent graduate degree

Minimum 0-3+ years of experience required

Basic competence with methodological approaches and tools in health services research is required, e.g., literature review, clinical data interpretation and claim data analysis

Knowledge of data science and/or health economic methodologies desirable

Knowledge of international health systems, health technology assessment, and pharmaceutical economics preferable

Experience with using Microsoft Excel, Word, and PowerPoint

Excellent oral and written English communication skills required

Ability to manage multiple projects involving complex processes, significant budgets, competing deadlines and rapidly shifting priorities in a compliant manner

Be self-directed and able to work without close supervision/support

Strong interpersonal and time-management skills

Understanding of V&E methods preferred

Understanding of clinical and observational study designs and analyses preferred

Location:

This is a hybrid position, candidates must be able to come on-site at the Pharmaceutical headquarters in New York, NY for in-person meetings typically 1-2 times every week

There is the potential for occasional travel to meetings including domestically and/or overseas, although this would be determined on a case-by-case basis according to needs