Responsable Ressources Humaines (CDD) H / F

Responsibilities:

• Monitoring independently different sites, including RBM
• Participation in investigator meetings as necessary
• Ensuring the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, SOPs, etc.
• Ensuring effective communication between investigational sites and internal/external stakeholders
• Working on project work and initiatives for process improvement as required

Requirements:

Education and Experience:

• Degree in pharmacy, life science, or related field
• 0 – 1 years’ clinical monitoring experience
• Fluency in English and French
• Ability to work in a combination of office and home-based settings in the Paris area

Knowledge, Skills and Abilities:

• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Excellent understanding and demonstrated application of GCPs and applicable SOPs
• Management of regulatory and/or IEC questions
• Development and preparation of the local informed consent form
• Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
• Management of the delivery of study supplies
• Effective interpersonal skills
• Strong attention to detail
• Effective organizational and time management skills
• Proven flexibility and adaptability
• Ability to work in a team or independently as required
• Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software