Senior Study Specialist (m/f/x) - Clinical Trial Supply

Behringwerke AG; Marburg; Hybrid; EUR 60.000 - 90.000; Vollzeit

Zusammenfassung

Behringwerke AG is seeking a Senior Study Specialist for their Global Supply Chain division. This role involves planning and monitoring logistics for clinical trials, ensuring compliance, and collaborating with various stakeholders. Candidates should have a Bachelor of Science degree and significant experience in clinical research and logistics.

Leistungen

Well-being programs

Diverse and inclusive workplace

Qualifikationen

• 4-5 years of professional experience in clinical research and logistics.
• Knowledge in GCP/cGMP/GDP/ICH.
• Experience in global project management, ideally in R&D.

Aufgaben

• Planning and monitoring logistics for global clinical trials.
• Coordination of trial supply with internal and external partners.
• Ensuring compliance with SOPs during clinical activities.

Kenntnisse

Project Management

Logistics

Communication

Presentation Skills

Fluency in English

Ausbildung

Bachelor of Science degree (biology or logistics)

Jobbeschreibung

For our Global Supply Chain (Clinical Trial Supply) division, we are currently looking for a

Senior Study Specialist (m/f/x) - Clinical Trial Supply

Job ID: R-253043

Fulltime / Permanent

Multiple locations and hybrid working models available

Tasks and Responsibilities

1. Planning, implementation, and monitoring of a logistics network for assigned simple global clinical trials, including:

• Coordination of worldwide trial supply with internal global departments and external service providers
• Participation in or, if necessary, leading meetings with internal and external expert groups for the provision of clinical trial supplies

Collaboration on complex global studies in coordination with the supervisor

Implementation and monitoring of the entire trial supply chain at the study sites, including:

• Creation and revision of study documents
• Training of internal and external stakeholders regarding the handling of the respective product

Ensuring SOP-compliant execution of all assigned clinical study activities

Collaboration in the preparation, execution, and follow-up of audits and inspections

Participation in the creation and revision of study-specific software specifications in an IRT system (Interactive Response System)

Calculation and monitoring of the budget for assigned studies

Technical collaboration in cross-country and cross-functional projects (e.g., continuous improvement regarding clinical trials and clinical trial goods management)

Education and Skills

• Bachelor of Science degree, e.g., biology or logistics
• At least 4-5 years of professional experience in clinical research and logistics within the biopharmaceutical industry
• Additional experience in global project management, ideally in an R&D environment
• Knowledge and experience in GCP/cGMP/GDP/ICH
• Fluency in English
• Good presentation skills

Further information can be found below under ‘What we offer’.

Please apply online with your complete application documents (CV and references), salary expectations, and notice period.

We look forward to receiving your application!

Our Benefits

We encourage you to prioritize your well-being. It’s important, and so are you. Learn more about how we care at CSL.

About CSL Behring

CSL Behring is a global leader in developing and delivering high-quality medicines for people with rare and serious diseases. Our treatments are available in over 100 countries, addressing conditions in immunology, hematology, cardiovascular and metabolic, respiratory, and transplant areas. Learn more about CSL Behring.

We strive for a diverse and inclusive workplace. Learn more about Inclusion & Belonging at CSL.

Join us and do work that matters at CSL Behring!