We are currently seeking a Junior Trial Manager (m/f/d) on behalf of our business partner in the pharmaceutical industry, located in Biberach .
Here's what we offer
* Attractive salary and long-term job security through affiliation with a large corporation.
* Up to 30 days of vacation per year
* Company pension scheme contribution after the end of the probationary period
* Extensive social benefits, including Christmas and holiday pay
* Reimbursement of travel expenses
* Usually an open-ended employment contract
* Good opportunities for acquisition with our business partners
* Tailored professional development opportunities and free language courses
* A wide range of employee benefits
Your tasks
* In your new role, you will be responsible for the global supply chain activities for purchased market products that complement Boehringer's investigational medicinal products (IMPs) in national and international clinical trials as comparators (active comparators, non-IMP commercial products) for chemical products.
* You are the contact person for CDO (Clinical Development Operations) for assigned studies and ensure the timely and cost-effective provision of clinical material.
* They ensure cross-functional collaboration and the development of interfaces for all supply chain activities based on business, regulatory and industry-related requirements.
* Thanks to your expertise, you contribute to clinical trial protocols and procurement processes, including a focus on comparator products and non-IMP commercial products, specific packaging designs, and efficient delivery strategies.
* Furthermore, as a specialist in the supply chain of hospital supplies, you will support clinical development / medicine at Boehringer Ingelheim.
Your profile
* Master's or Bachelor's degree in natural sciences, ideally with experience in clinical trials and activities in the IMP supply chain
* Experience in an international environment and project management experience to lead a matrix team, as well as the ability to interpret complex project requirements.
* Good knowledge and understanding of the regulatory and GMP/GCP requirements for IMPs
* Fluent English, both spoken and written; German is an advantage.
* Good MS Office skills
* Strong problem-solving skills, decision-making ability and results orientation
* Excellent communication, negotiation and presentation skills – especially in high-pressure situations.
Standort
GULP – experts united, Biberach