Program Manager, Clinical Supply Chain Management (all genders) (full-time, regular)

AbbVie Inc.; Ludwigshafen am Rhein; Hybride; EUR 90 000 - 120 000; Plein temps

Avantages offerts par ce poste

Diverse work environment

Open corporate culture

Attractive salary

Mentor onboarding

Flexible work models

Corporate health management

Company social benefits

Career opportunities in international"

Top-tier development opportunities

Strong international network

Résumé du poste

AbbVie Germany is seeking a Program Manager for Clinical Supply Chain Management to lead the global clinical supply strategy for early-phase programs and ensure on-time delivery to sites.

You will work with cross-functional teams, manage budgets, and help bring therapies to patients, requiring 5-7+ years in pharma and strong leadership.

Qualifications

• Bachelor’s Degree or higher in Pharmacy or Science.
• 5-7+ years’ experience in the pharmaceutical industry.
• Demonstrated understanding of the overall drug development process.
• Experience in project management, planning, forecasting, budgeting.
• Excellent interpersonal, team, and leadership skills.
• Sound knowledge of GxP.

Responsabilités

• Define and implement a global clinical supply strategy, in conjunction with mentor or experienced Drug Supply Manager
• Ensure all clinical supplies (early phase, 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)
• 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 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

Connaissances

Drug development process

Project management

Forecasting

Budgeting

Leadership skills

GxP knowledge

Formation

Bachelor’s Degree or higher in Pharmacy or Science

Description du poste

Company Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, XandYouTube.

Job Description

People. Passion. Possibilities. Three words that make a world of difference.

More than a job. It's a chance to make a real difference.

Welcome to AbbVie! As part of an international company with 57,000employees worldwide and around 3,500 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place!

Together, we break through – as Program Manager, Clinical Supply Chain Management (all genders)

The Program Manager, Clinical Supply Chain Management’s primary responsibility is to manage the clinical supply chain for early phase (uncomplicated) 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.

Make your mark:

• Define and implement a global clinical supply strategy, in conjunction with mentor or experienced Drug Supply Manager
• Ensure all clinical supplies (early phase, 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)
• 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 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

Qualifications

This is how you make a difference:

• Bachelor’s Degree or higher in Pharmacy or Science
• 5-7+ years’ experience in the pharmaceutical industry
• Demonstrated understanding of the overall drug development process
• Experience in project management, planning, forecasting, budgeting
• Excellent interpersonal, team, and leadership skills
• Sound knowledge of GxP

What we offer you:

• with a diverse work environment where you can have a real impact
• with an open corporate culture
• with an attractive salary
• with an intensive onboarding process with a mentor at your side
• with flexible work models for a healthy work-life balance
• with a corporate health management that offers comprehensive health and exercise programs
• with company social benefits
• with a wide range of career opportunities in an international organization
• with top-tier, attractive development opportunities
• with a strong international network

At multiple times, we have been globally recognized as a "Great Place to Work" and we are proud to provide our employees with the flexibility to maintain a healthy work-life balance. We take our impact on the environment and our communities seriously and therefore focus on giving something back on a regular basis. We are committed to equality, equity, diversity and inclusion (EED&I) – a commitment that is fundamental to us. This includes appreciating different perspectives, creating an inclusive culture and treating all employees with dignity and respect.

At AbbVie, your individual contributions count – help us move mountains together. Be a part of our success, grow with us and accomplish more than you could have imagined.

Additional Information

AbbVie 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

Any questions? Feel free to email [e-mail] – we look forward to hearing from you!