(Senior) Clinical Project Manager
CureVac
Tübingen or Wiesbaden, Germany
Your Responsibilities:
- Manage national and/or multinational clinical trials with innovative vaccines in the field of oncology/infectious diseases
- Ensure adherence to timelines, quality, and regulatory requirements in cooperation with the Clinical Project Team
- Manage project aspects such as budgeting, contracting, drug supply, recruitment, and study progress
- Interact with CROs as well as vendors and internal stakeholders as needed
- Guarantee compliance with clinical trial protocol, check clinical site activities and progress, conduct on-site visits
- Support the Clinical Project Team with regards to vendor oversight
- Lead complex and high-priority projects in early stages of development and set the overall strategic and tactical direction for the area of responsibility
- Control budget- and contract-related tasks proactively, independently and without supervision
Your Qualifications:
- Bachelor's or master's degree in pharmacy, natural sciences, medicine, a related field or an equivalent qualification
- Several years of relevant job experience in a similar role in a CRO and/or biotech or pharma company
- Strong comprehension of ICH-GCP; additional understanding of EU or US regulations and laws are an asset
- Good practical knowledge of MS Office, CTMS and eTMF
- Fluency in English; intermediate German skills are a plus
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