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

at  CureVac

Wiesbaden, Hessen, Germany -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate16 Nov, 2024Not Specified17 Aug, 2024N/AOpenness,Reliability,Medicine,Natural Sciences,EnglishNoNo
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Description:

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

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
    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.

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


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Wiesbaden, Germany