Clear and articulate verbal, written and presentation skills with good command of the English language and the appropriate comportment to represent UCB internationally at meetings and congresses
The MD will also play a major role in the pre-analysis meeting
Clinical Development Experience with Immunology, ideally PsA
Min 5 years of experience in pharmaceutical industry in clinical development including knowledge of GCP
If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer
Verantwortlichkeiten
Contribute to the clinical section of documents including, but not limited to, the Investigator Brochure , Annual IND Safety Updates/EU Annual Reports, Clinical Study Reports, and submission related documents such as the Clinical Summary of Efficacy and Safety and the Clinical Overview
Management
Anforderung
10+ years of experience in a CRO/pharmaceutical environment with a proven and consistent record of proactive management and innovation
3+ years of line management experience in a CRO/pharmaceutical environment with a successful record of developing personnel and teams
Active engagement with internal/external stakeholders to develop/implement/improve standard processes, controls, and systems related to Risk Management and RBM, in a CRO oversight model
3+ years of experience in the CRO/pharmaceutical environment related to the development/implementation of Risk-Based Monitoring related capabilities
Demonstrated experience analyzing and evaluating business relationships/situations to make decisions and determine appropriate responsive actions
Proven ability to develop and lead a multi-functional and geographically diverse team
Thorough knowledge and understanding of standards development processes, esp. for clinical data
If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation
Project Management
Anforderung
A minimum of 5 years of experience in the Pharmaceutical, Biotechnology and/or CRO industry is required
Clinical development experience as a Clinical Project Manager or a similar role is preferred
Relevant Bachelor’s degree needed with an advanced degree of PhD preferred
Acting as a Subject matter expert for special topics of interest
Ideally line management experience is preferred but not required
Proven track record of successfully leading cross-functional projects in a global environment
If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer
Facility Management
Anforderung
Financial acumen with a thorough understanding or experience of managing considerable budgets
Fluency in German and English
Knowledge of pharmaceutical regulatory matters
+3 years of experience in Real Estate Management
Provision of Records Management & Archiving services to German & Austrian affiliates Assist Head of Records Management in provision of services relating to on-site and off-site archiving of regulated GXP documents at a facility approved and audited by UCB Manage off-site contract archiving of other business, financial, legal records for all departments at site
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer
Teamleader
Anforderung
As an Analytical Teamlead you like to work in an environment where you can
Excellent command of written and spoken German and English
Very flexible and agile individual with high accountability
Flexibility to travel within Europe
Must have good managerial, organization, leadership and analytical skills
Good project management skills
Highly self-motivated and good team player
Independently drive development projects within PDS
Project Manager
Anforderung
Good interpersonal skills and excellent time management and organizational skills
Delivery of scientific/medical presentations and training to both large and small audiences
Ensuring a risk assessment is performed and a Risk Mitigation Plan is set-up at the beginning of the study and maintained by the partner CRO
Creating or contributing to detailed planning of the study, timelines, define critical path to enable seamless access to data, early read out of bioanalytical and safety data to enable data review meetings and early decision making
Proactive approach, drive and follow through
Relevant Bachelor’s degree needed with an advanced degree of PhD preferred
Scientific and technical knowledge: GCP and regulatory environment Medical knowledge and research expertise Basic principles of data management and statistics
Substantial experience in study management in different indications and proven ability to manage complex multinational studies or multiple simultaneous studies from start to end