Work at the forefront of pharmaceutical innovation! Join our dynamic team as a Program Lead and leverage your expertise to drive innovation in the areas of clinical trial supplies and investigational medicinal products (IMPs) management. Within the IMP Management Group in IMP Delivery you will take over the responsibility of a Program Lead for global Supply Chain activities for Investigational Medicinal Products (IMPs) of national and international Phase I-IV clinical trials NCE projects. Your expertise is our key to success!
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
Duties & Responsibilities• In your new role, you will act as the main point of contact to Drug & Device Project Management Lead and TA MED/Clinical Development & Operations for assigned projects/programs.
• One of your main task is to ensure the timely and cost-efficient provision of clinical supplies in these projects/programs.
• Within IMP Management, you will closely interact with study specific Clinical Trial Supply Managers to oversee the Clinical Supply Chain activities on a project/program level.
• Furthermore, you will represent IMP Management as primary contact and operate as sub team member for different Boehringer Ingelheim projects/programs.
• Moreover, you will be an active member in international development project teams.
• Through your expertise you will provide input to clinical trial protocols, bulk demands, incl. comparator and non-IMP commercial products and support regulatory submission.
• Additionally, you will be responsible for cost estimations and innovation.
• Diploma or Master Degree in relevant discipline, e.g., natural sciences, engineering, clinical sciences plus multiple years of function relevant experience.
• At least two (2) years relevant experience in Pharmaceutical industry.
• Demonstrates excellent knowledge of all areas of clinical supply chain activities and a thorough knowledge and understanding of applicable US and EU regulations
• Good knowledge and understanding of the regulatory and GMP/GCP requirements for IMPs
• Good oversight on neighboring disciplines (medical affairs, clinical development, regulatory affairs, production and supply chain, drug development, finance and controlling).
• Ability to interpret standard and complex project requirements.
• Ability to learn new technologies and concepts to enhance operations.
• Strong computer skills (e.g., Microsoft Office 365).
• Communicates effectively orally and in writing.
• Proven ability to present projects / status reports, to advice various expert functions, to successfully negotiate and convince within complex interdisciplinary and international project environment.
• Strong problem solving, risk assessment and troubleshooting skills.
• Proven ability to drive results in a changing environment.
• Willingness to travel.
• Very good to fluent in English, spoken and written.
• Ability to prioritize daily tasks and to manage challenging and stressful daily business.
Eligibility Requirements:
• Must be legally authorized to work in the United States without restriction.
• Must be willing to take a drug test and post-offer physical (if required).
• Must be 18 years of age or older.
This position offers a base salary typically between $102,000 and $175,000. The position may be eligible for a role specific variable or performance-based bonus and or other compensation elements. For an overview of our benefits please click here.