Aktuelle Jobs im Zusammenhang mit Senior Clinical Project Leader - Wiesbaden, Hessen - CureVac
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Senior Clinical Project Manager
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Wiesbaden, Hessen, Deutschland CureVac VollzeitCureVac SE is a global biopharmaceutical company researching and developing novel drugs based on the natural molecule Messenger RNA (mRNA). Our focus is on prophylactic vaccines, innovative cancer immunotherapies, and protein-based therapies.To strengthen our team, we are currently looking to recruit a Clinical Project Manager to manage national and/or...
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Wiesbaden, Hessen, Deutschland CureVac VollzeitCureVac SE is a global biopharmaceutical company dedicated to developing innovative vaccines and treatments. We are seeking a highly skilled Clinical Project Manager to join our team in Tübingen or Wiesbaden.Your Key Responsibilities:Manage national and international clinical trials for innovative vaccines in oncology and infectious diseasesEnsure timely...
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Wiesbaden, Hessen, Deutschland CureVac VollzeitCureVac SE is a global biopharmaceutical company dedicated to developing innovative vaccines and treatments. We are seeking a highly skilled Clinical Project Manager to join our team in Tübingen or Wiesbaden.Your Key Responsibilities:Manage national and international clinical trials for innovative vaccines in oncology and infectious diseasesEnsure timely...
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Senior Clinical Project Leader
vor 3 Monaten
Company Overview:
CureVac SE is a pioneering biopharmaceutical organization dedicated to the research and development of innovative therapies utilizing Messenger RNA (mRNA). Our primary focus encompasses the creation of preventive vaccines, cutting-edge cancer immunotherapies, and protein-based treatments.
Position Overview:
We are seeking a highly skilled
(Senior) Clinical Project Manager (f/m/d)
to enhance our operations in Tübingen or Wiesbaden.
Key Responsibilities:
- Oversee national and international clinical trials involving innovative vaccines targeting oncology and infectious diseases.
- Ensure compliance with timelines, quality standards, and regulatory guidelines in collaboration with the Clinical Project Team.
- Manage various project components, including budgeting, contracts, drug supply, participant recruitment, and study progression.
- Engage with Contract Research Organizations (CROs), vendors, and internal stakeholders as necessary.
- Ensure adherence to clinical trial protocols, monitor clinical site activities, and conduct site visits.
- Assist the Clinical Project Team in vendor management and oversight.
- Lead complex, high-priority projects in the early stages of development, establishing strategic and tactical direction for the assigned area.
- Proactively manage budget and contract-related responsibilities independently.
Qualifications:
- Bachelor's or master's degree in pharmacy, natural sciences, medicine, or a related discipline, or an equivalent qualification.
- Extensive experience in a similar role within a CRO, biotech, or pharmaceutical company.
- Strong understanding of ICH-GCP guidelines; familiarity with EU or US regulations is advantageous.
- Proficient in MS Office, Clinical Trial Management Systems (CTMS), and electronic Trial Master Files (eTMF).
- Fluent in English; intermediate proficiency in German is a plus.
We offer a challenging and diverse opportunity within an innovative and dynamic organization that is on the rise. Our team is dedicated to making significant contributions to the medical field, fostering a culture of mutual respect, reliability, and personal initiative.
CureVac SE
