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Our client, a world-leading Pharmaceutical Company in New York, NY is currently looking for a Research Associate / HEOR- Health Economics and Outcomes Research / HYBRID WORK to join their expanding team.
Job Title: Research Associate / HEOR- Health Economics and Outcomes Research / 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:
Position Summary:
Pharmaceutical 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.
Position Responsibilities:
Conducts literature reviews to understand burden of illness and estimate 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 burden of disease to support the 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 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
Manages 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.
Organizational Relationships:
Pharmaceutical Global GAV team
V&E Global Directors and Senior Directors for DMD GTx
Global GAV lead for DMD GTx
Global Medical colleagues for DMD GTx
Global RWE CoE (Real World Evidence Centre of Excellence) colleagues
Medical and V&E Country colleagues for DMD GTx
Pharmaceutical colleagues acting as center of excellence for Pharmaceutical systems (eg ENGAGE, POD)
External stakeholders
KOLs working on DMD GTx studies and projects (varies according to project)
Technical Skills Requirements:
Required:
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 budget, 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
Preferred:
Understanding of V&E methods
Understanding of clinical and observational study designs and analysis
Physical Position Requirements:
Pharmaceutical headquarters is in New York, NY in the US, with in-person meetings typically 1-2 times every week.
The V&E Team otherwise works virtually. The candidate should be able to perform general office activities (work at a desk, attend meetings via Teams).
There is the potential for occasional travel to meetings including domestically and / or overseas, although this would be determined on case-by-case basis according to need.
Interviews:
Round 1: Teams interview with team
Round 2: Teams interview with team leader
