Trial Manager (m/f) Clincal Trial Supplies Unit

Job description

Description

As Trial Manager (m/f) CTSU youare responsible for the global supply chain activities for Investigational Medicinal Products (IMPs) of national and international phase II to IV clinical trials in the Therapeutic Areas Cardiovascular and Metabolic. With your experience regarding working in an international environment you act asthe main point of contact to Clinical Operations and Clinical Development for assigned trials, ensure the timely and cost efficient provision of clinical supplies and also collaborate withexternal contract manufacturing organization on outsourced supply chain activities.

The position is initially limited until December 2017.

Duties & Responsibilities

·  Within the matrix structure you are the responsible leader of the CTSU trial team where you ensure cross-functional collaboration and development of interfaces for all Supply Chain activities on the basis of business, regulatory and industry needs.
·  You provide input to clinical trial protocols, selection of most suitable comparator and non-IMP commercial products, develop specific packaging designs and efficient distribution strategies.
·  With regards to bulk manufacturing scenarios based on trial-specific bulk requirements you closely collaborate with CTSU Project Managers.
·  You support investigations as Subject Matter Expert for assigned trials.

Our Culture

Boehringer Ingelheim is a research-driven pharmaceutical company and one of the top 20 pharmaceutical firms worldwide. Headquartered in Ingelheim, Germany, Boehringer Ingelheim operates globally in over 100 countries and has more than 47,700 employees. The focus of the family-owned company, founded in 1885, is researching, developing, manufacturing and marketing new medications of high therapeutic value for human and veterinary medicine. In 2014, Boehringer Ingelheim achieved net sales of about 13.3 billion euros. R&D expenditure corresponds to 23.1% of its net sales.

Contact

Boehringer Ingelheim is an equal opportunity employer who takes pride in maintaining a diverse and inclusive workplace. We embrace all aspects of diversity and inclusion which benefit our employees, patients and communities. We look forward to receiving your online application!

For further information please contact Recruiting Services.
Tatjana Blersch, Phone: +49 (0) 7351 54-4386

Desired profile

Requirements

·  Bachelor's degree in Pharmaceutics, Biology or completed vocational training with experience in clinical trials
·  Good knowledge and understanding of the regulatory and GMP/GCP requirements for IMP
·  At least 2 year experience in clinical trial supplies business
·  Experience in team leading and project management
·  Ability to interpret complex project requirements
·  Strong problem solving capabilities with the willingness to make decisions and the ability to drive results
·  Fluency in written and spoken English and German
·  Very good communication, negotiation and presentation skills
·  Ability to work independently as well as in a team