CAREERS

Jan 22

Assistant for Development activities

Activities Manage clinical and regulatory documents layout, formatting, reference listing and publishing Provide operational support and coordinate administrative activities related to clinical studies throughout the life-cycle of the clinical trial Tracking, filing and archiving of administrative, clinical and regulatory documents associated with the field of activity Maintain Clinical Trial Master... read more →
Jan 22

Quality assurance trainee

Function Description We are looking for a quality assurance intern. The objective of the internship is to help the CMC (Pharmaceutical Synthesis) team and the Clinical team to set up a quality management system under the direction of the quality manager dedicated to research activities. Tasks In collaboration with the... read more →
Jan 22

Patent Engineer Intern

Duration : January 2020-July / August 2020 Paris, France Attached to the Patent Manager (European Patent Agent), your main missions will be : Participation in patentability / freedom to operate studies Analysis of research reports and official notifications Competitive and technological watch activities Realization of a synthesis on a... read more →
Jan 22

Regulatory Affairs Manager – Junior

Roles and responsibilities Under the responsibility of the regulatory affairs Director: You will take in charge the coordination and the tracking of regulatory activities related to CTA/IND submission in collaboration with the other departments (clinical operations, clinical development, pharmaceutical operations …) including:  Preparation, review and validation of CTA, IND... read more →
Jan 22

Technical and regulatory affairs officer

Function Description Tasks  Coordinate with the pharmaceutical development team and service providers (CMO) the information to constitute the pharmaceutical / quality part of the products under development then ultimately constituting the registration files. Write in English the regulatory part Module 3 CTD format of clinical trial / registration request files... read more →