Trainee specialist, CLS Global medical writing (cencora)

Roles and Responsibilities

Job Responsibilities:

• To perform systematic literature search for regulatory or scientific documents.

• To assist managers in the preparation of pre-clinical or clinical sections of the marketing authorization dossier.

• To assist the manager and preparation of various toxicology assessments like PDE/OEL or other toxicology documents

• To assist managers in preparation of other medical-scientific documents (e.g., publications, product rationales, medico-marketing material).

• The employee agrees to take over additional reasonable tasks that align with their abilities, if required

Skills & Knowledge:

• Autonomous, concentrated and high-quality work

• Ability to work in a team

• Sense of responsibility

• Basic knowledge of marketing authorization procedures in the EU

• Basic knowledge of economic principles

• Very good command of English

• Strong communication and interpersonal skills

• Excellent in MS Office package and well-versed with various literature