Overview

Design. Progress. Together.

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 Wiesbaden, we are currently looking to recruit an

Your responsibilities:

Fulfilling all Drug Safety activities for investigational compounds towards respective Regulatory Authorities
Contact point for all Drug Safety matters for investigational compounds as assigned within CureVac and for business partners
Develop and contribute to risk management strategies for investigational compounds and market products
Collaborate with CureVac Interface departments to further strengthen processes as applicable
Oversight of respective Pharmacovigilance (PV) service providers and/or business partners acting on behalf of CureVac
Support PV activities for CureVac’s investigational medicinal products (and market/authorised medicinal products) specifically in the collection, reporting and analyses of safety data; identifying, detecting and investigating safety signals
Single case safety review, aggregated periodic safety review in clinical trials as well as for marketed/authorised medicinal products including signal detection, validation and assessment, continuous risk benefit evaluation, safety analysis for assigned products
Support development of the PV quality assurance system required to ensure the company’s compliance with respect to patient safety laws, regulations and guidance associated with the development and licensure of the company’s medicinal products
Knowledge in and compliance with PV relevant regulations
Support audits and Health authority inspections

Your qualifications:
MD or Life Science degree or equivalent qualification
Several years of experience as a Drug Safety professional with focus on clinical safety, but also PV background in pharma/biotech and/or CROs
Independent working style but also a team player
Strong communication and presentation skills
Detail-oriented way of working and problem-solving and pragmatic attitude
Flexible and used to changing priorities
Fluency in English, German is 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 a given for us.

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

We look forward to receiving your application via our CareerPortal.

CureVac SE

Human Resources
Julia Daake

Friedrich-Miescher-Straße 15
72076 Tübingen

www.curevac.com