For our Department Clinical Regulatory Affairs at the company´s headquarters in Baden-Baden we are seeking to appoint a Clinical Regulatory Affairs Coordinator (f/m).
Your tasks:
Planning, coordination and release of clinical and nonclinical Expert Reports for regulatory procedures of Heel’s homeopathic products
Answering queries of Competent Authorities
Review of relevant medical and scientific literature
Providing scientific and medical expertise for regulatory tasks
Providing input for patient information leaflets and SPC
Providing clinical support e.g. for Pharmacovigilance / Drug Safety, Clinical Development
Surveillance of international regulatory developments
Contribution to further evolution of Heel’s product portfolio
Your profile:
University degree in pharmacy, preferably followed by a Ph.D.
Interest in working in a highly regulated environment
Sound written and verbal communication skills in German and English
Effective organization and planning skills
Reliable and integrative working attitude
High degree of team spirit and motivation
We offer in return a responsible, challenging field of activity, performance-related remuneration and the social benefits of a progressive, expanding company.
The position is for now limited to two years. In case of adequacy the transfer to a permanent employment contract is sought.
Are you interested?
If so please send your online application stating your salary expectation and the earliest possible start date to Maria Ammerlaan, Human Resources.
