採用
Career Category
Regulatory
Job Description
Job Description:
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.
Regulatory Writing Senior Manager
Live
What you will do
Let’s do this. Let’s change the world. In this key role you will serve as the functional area lead on product teams, lead writing activities for complex product submissions, provide functional area expertise, train and mentor more junior writers, and lead departmental activities. Key responsibilities include:
-
Author or oversee the authoring of all regulatory submission documents including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed Consent Forms, Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, and Pediatric Investigation Plans
-
Conduct the formal review and approval of authored documents, following applicable standard operating procedures
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With limited supervision, lead regulatory writing activities for complex product submissions, including new and supplemental drug applications/biologics license applications
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Serve as functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group)
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Provide functional area input for Global Regulatory Plan and team goals
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Supervise the work of contract and freelance writers and mentor junior medical writers as assigned
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Lead departmental and cross-departmental initiatives, as appropriate
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Generate document timelines
Win
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.
Basic Qualifications:
Doctorate degree and 2 years of directly related experience
OR
Master’s degree and 6 years of directly related experience
OR
Bachelor’s degree and 8 years of directly related experience
OR
Associate’s degree and 10 years of directly related experience
Or
High school diploma / GED and 12 years of directly related experience
Preferred Qualifications:
-
Experience with regulatory documents in Regulatory Affairs, Research, Development or related area
-
5+years of experience in medical writing in the Biotech/Pharmaceutical industry
Thrive
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.
Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:
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Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
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A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
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Stock-based long-term incentives
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Award-winning time-off plans and bi-annual company-wide shutdowns
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Flexible work models, including remote work arrangements, where possible
Apply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
careers.amgen.com
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
.
Salary Range
152,684.00 USD - 193,308.00 USD
総閲覧数
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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Amgenについて

Amgen
PublicA biotechnology company that develops and manufactures human therapeutics for various illnesses and diseases.
10,001+
従業員数
Thousand Oaks
本社所在地
$138B
企業価値
レビュー
3.6
10件のレビュー
ワークライフバランス
3.2
報酬
4.1
企業文化
3.4
キャリア
2.8
経営陣
3.5
65%
友人に勧める
良い点
Excellent benefits and health benefits
Good pay and compensation
Supportive management and strong leadership
改善点
Limited career growth and promotion opportunities
Work-life balance challenges and long hours
Bureaucratic processes
給与レンジ
1,244件のデータ
Senior/L5
Senior/L5 · Clinical Research Medical Director
1件のレポート
$374,000
年収総額
基本給
$288,425
ストック
-
ボーナス
-
$374,000
$374,000
面接体験
5件の面接
難易度
3.0
/ 5
期間
14-28週間
内定率
40%
体験
ポジティブ 20%
普通 80%
ネガティブ 0%
面接プロセス
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Technical/Role-Specific Interview
5
Panel Interview
6
Offer
よくある質問
Technical Knowledge
Behavioral/STAR
Past Experience
Data Analysis/Statistics
Culture Fit
ニュース&話題
Amgen (AMGN) Laps the Stock Market: Here's Why - Yahoo Finance Singapore
Yahoo Finance Singapore
News
·
4d ago
UBS Sees Continued Upside in Amgen (AMGN), Lifts Target to $400 - Insider Monkey
Insider Monkey
News
·
4d ago
Amgen Inc. $AMGN Shares Sold by Whittier Trust Co. - MarketBeat
MarketBeat
News
·
4d ago
AE Wealth Management LLC Has $43.90 Million Holdings in Amgen Inc. $AMGN - MarketBeat
MarketBeat
News
·
5d ago