채용
The Associate Director, Clinical Supply Chain Management’s primary responsibility is to manage the clinical supply chain for Phase 1 to Phase IV compounds. The completion of clinical trials is the rate-limiting step for filing of new drug applications and, ultimately, to product commercialization. The on-time initiation, uninterrupted conduct, and completion of clinical studies is dependent on the timely delivery of clinical supplies of top quality to the clinical sites.
Responsibilities
- Define and implement a global clinical supply strategy, including the development of strategic options for the clinical supply chain.
- Ensure all clinical supplies (Phases I-IV, affiliate studies, and IIS) are delivered on time, on budget and of top quality with no studies interrupted or delayed due to clinical supplies
- Define and manage external budget for compounds (comparators, co-meds, over-encapsulation, depots, and importation costs)
- Represent the clinical supply chain on Integrated Evidence Strategy Teams (IESTs) and participate and contribute to Product Presentation and Device Strategy Team (PPDST) meetings
- Define API and drug product requirements and delivery dates to support the clinical supply chain
- Matrix management of a larger number of Clinical Supply Project Managers (CSPMs) supporting the global clinical supply chain
- Allocate bulk drug product to CSPMs, minimizing wastage
- Lead the recovery of clinical supplies during a product recall, support the evaluation and approval of non-medical complaints (NMCs), exception reports and recalls
- Demonstrate leadership skills by driving for continuous improvement and encouraging and supporting collaboration across departments. Represent CDSM Program Management on cross-functional and global initiatives which require clinical drug supply expertise.
- Bachelor’s Degree or higher in Pharmacy or Science.
- 8+ years’ experience in the pharmaceutical industry, preferably with CMC and/or clinical supplies management experience.
- Broad understanding of the overall drug development process.
- Experience in project management, planning, forecasting, budgeting.
- Excellent interpersonal, team, and leadership skills.
- Sound knowledge of GxP.
Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
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AbbVie 소개

AbbVie
PublicPharmaceutical company.
10,001+
직원 수
North Chicago
본사 위치
$200B
기업 가치
리뷰
3.2
10개 리뷰
워라 밸
3.2
보상
4.1
문화
2.8
커리어
2.9
경영진
2.3
45%
친구에게 추천
장점
Good compensation and benefits
Strong leadership potential
Good facilities and resources
단점
Poor management and leadership issues
Toxic work environment
Frequent policy and organizational changes
연봉 정보
88개 데이터
Junior/L3
Mid/L4
Intern
Director
Junior/L3 · Associate Business Systems Consultant
4개 리포트
$167,325
총 연봉
기본급
$145,500
주식
-
보너스
-
$141,860
$170,567
면접 경험
4개 면접
난이도
3.0
/ 5
소요 기간
14-28주
경험
긍정 0%
보통 25%
부정 75%
면접 과정
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Panel Interview
5
Offer
자주 나오는 질문
Behavioral/STAR
Past Experience
Culture Fit
Technical Knowledge
뉴스 & 버즈
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