Senior Clinical Project Leader

Senior Clinical Project Leader

Bavarian Nordic

Planegg, Germany

As a Senior Clinical Project Leader (m/f/d) you are regularly responsible for “your” study and lead a project team of internal and external partners.

Forward thinking Project Leader with a knack for compliance and communication alike

Your Responsibilities

  • With minimal oversight, plan and manage clinical trials to ensure studies are completed on time/within budget and ensures that everything is completed according to the clinical development strategy to ensure regulatory approvals
  • Responsible for study related in-house collaboration and coordination of cross-functional groups (Manufacturing, Quality Assurance, QC-D Development, Bioanalysis, Operations, Finance, Commercial and respective stakeholders from Research and Development)
  • Responsible for having knowledge of and being in compliance with BN SOPs and GCPs as well as relevant regulatory requirements
  • Oversee and manage CROs, study contractors and vendors - including issue escalation/resolution and budget negotiations
  • Responsible for collection of study metrics as well as developing reports and delivering presentations as requested
  • Accountable for applying new processes or business strategies to assigned tasks or activities
  • Responsible for identifying issues and proposing ideas to manage risks to clinical study/program, timelines, budget and corporate goals
  • Participate in the training/mentoring of staff involved in clinical trial management

Skills

  • Comfortable working in international environments, with team members located in different locations/countries, travelling will be required
  • Established track record of generating alternative solutions and understanding different perspectives at study level
  • Encourage others within the team to seek alternative perspectives and develop solutions
  • Able to take information from various sources on a study, review/analyze information and present conclusions/outcomes/next steps
  • Strong leadership skills, for example allocate decision-making authority and task responsibilities to other team members as appropriate.
  • Ability to track multiple items and provide guidance on the prioritization of tasks within a study, able to work with various groups internally and externally to get tasks completed

Your Profile

  • Minimum of 4 years of experience in clinical research and drug development as well as a minimum of 1-year study management experience required
  • CRA experience and vaccine experience, at least 3 years in study management preferred
  • Excellent verbal and written communication skills hat demonstrate tact and diplomacy
  • Must be fluent in English.
  • Must be highly organized

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© EuroJobsites 2021

EuroJobsites is a registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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