(Senior) Clinical Project Manager (f/m/d)

CureVac; Wiesbaden; Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

Join a forward-thinking biopharmaceutical company dedicated to revolutionizing medicine through innovative mRNA therapies. As a Senior Clinical Project Manager, you will lead complex clinical trials, ensuring compliance with regulatory standards while managing budgets and contracts effectively. This dynamic role offers the chance to work on groundbreaking projects in oncology and infectious diseases, collaborating with a passionate team committed to making a difference. If you're ready to shape the future of healthcare and thrive in a culture of openness and respect, this opportunity is for you.

Qualifikationen

• Several years of relevant experience in a CRO or biotech company.
• Strong understanding of ICH-GCP and EU/US regulations.

Aufgaben

• Manage national and multinational clinical trials for innovative vaccines.
• Ensure adherence to timelines and regulatory requirements.

Kenntnisse

Clinical Trial Management

Budget Management

Regulatory Compliance

Project Management

Fluency in English

Intermediate German Skills

Ausbildung

Bachelor's or Master's Degree in Pharmacy or Natural Sciences

Tools

MS Office

CTMS

eTMF

Jobbeschreibung

CureVac 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. Currently, all RNA people are striving to achieve our main goal : To bring multiple best-in-class mRNA drugs to market.

To strengthen our team in Tübingen near Stuttgart or Wiesbaden, we are currently looking to recruit a

Senior) Clinical Project Manager (f / m / d)

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 fieldor 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

We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding.

With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us.

Design your future with us – become part of the RNA people!

We look forward to receiving your application via our CareerPortal.