採用
福利厚生
•Healthcare
•Equity
•Unlimited Pto
必須スキル
HTA
Systematic literature review
Indirect treatment comparison
Meta-analysis
Cost-effectiveness modeling
Evidence synthesis
As a Senior Manager, HEOR you will contribute to the development of our evidence packages for HTA submissions facilitating product access, reimbursement, and differentiation. Responsibilities involve supporting our evidence synthesis projects (e.g., systematic literature review, meta-analyses, indirect treatment comparisons). We also support cost-effectiveness models, and working closely with our global and regional partners aligning HEOR strategies with market requirements.
This position is located at our Sleepy Hollow, NY office and is on-site for 4 days/week. We cannot offer a hybrid or fully remote options. If eligible, we can offer relocation benefits.
A typical day may include the following:
- Participate in the development of our observational research studies, cost-effectiveness, and budget impact models, to support reimbursement dossiers.
- Collaborate with cross-functional our business partners to develop and support product value propositions that optimize access, reimbursement, and uptake, ensuring alignment with HTA requirements.
- Identify HEOR evidence gaps and design studies and tools to demonstrate relative value and product differentiation for submissions.
- Develop and implement HEOR strategies to support commercialization activities, including the preparation of HTA submissions and addressing payer requirements.
- Evaluate HTA decisions and apply insights to pipeline and marketed products, ensuring submissions meet regulatory and payer expectations for value demonstration and reimbursement.
- Report, publish, and present HEOR data and study results, ensuring compliance with regulatory standards and effectively communicating evidence to collaborators.
This may be for you if you:
- Want to have an impact on patient lives
- Enjoy working in a ‘rapid response’ environment
- Can demonstrate knowledge of HTA, SLR and ITC
- Would like an opportunity to present to senior leaders
To be considered you are to have a Master’s degree in an HEOR related major with a PhD or PharmD being. Your experience needs to include 2+ years of experience in the pharmaceutical industry or in a HEOR consulting organization. Experience required includes the design and conduct of evidence synthesis projects and knowledge of pairwise and network meta-analysis, as well as population-adjusted indirect comparison. Experience in developing and managing HEOR projects that align with the ISPOR guidelines and support HTA regulatory submissions (e.g., NICE) is helpful. Customer-facing experience at country level is required. US managed care experience is a strong advantage.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Salary Range (annually)
$148,300.00 - $241,900.00
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0
応募クリック数
0
模擬応募者数
0
スクラップ
0
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Regeneronについて

Regeneron
PublicRegeneron Pharmaceuticals, Inc. is an American biotechnology company headquartered in Westchester County, New York. The company was founded in 1988.
10,001+
従業員数
Westchester County
本社所在地
$76B
企業価値
レビュー
3.1
10件のレビュー
ワークライフバランス
2.8
報酬
3.2
企業文化
2.9
キャリア
3.5
経営陣
2.7
55%
友人に勧める
良い点
Great science and people
Good learning environment
Supportive management
改善点
Bullying and blame culture
Inconsistent culture across sites
Understaffing and burnout
給与レンジ
802件のデータ
Entry Level
Junior/L3
Mid/L4
Senior/L5
Intern
Director
Entry Level · Lab Technician
0件のレポート
$95,475
年収総額
基本給
$95,475
ストック
-
ボーナス
-
$81,050
$109,900
面接体験
1件の面接
難易度
3.0
/ 5
期間
14-28週間
面接プロセス
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Technical Assessment
5
Panel Interview
6
Offer
よくある質問
Behavioral/STAR
Technical Knowledge
Past Experience
Culture Fit
ニュース&話題
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