Ofertas de empleo en Barrington James

• Flexibilidad horariaSí
• Nivel de experiencia---
• Tipo de contratoA tiempo parcial
• PublicadaNueva

Overview

I am seeking a professional and experienced Clinical Research Associate to join the team in Spain for a respected Sponsor company I am partnered with. This is a freelance, part-time position with a 0.5 FTE commitment for a 12-month duration. The successful candidate will be responsible for regulatory activities related to clinical trials.

Responsibilities

• Oversee regulatory compliance for clinical trials in accordance with local and international regulations
• Coordinate with regulatory authorities and ethics committees for approvals and submissions
• Ensure documentation and reporting are in line with regulatory requirements
• Conduct site visits to assess regulatory compliance and provide support and guidance to site staff
• Collaborate with cross-functional teams to ensure regulatory milestones are achieved
  
  

• Bachelor's degree in a scientific or healthcare discipline
• Proven experience as a Clinical Research Associate in regulatory activities
• In-depth knowledge of regulatory requirements for clinical trials in Spain
• Strong understanding of ICH-GCP guidelines and other relevant regulations
• Excellent communication and interpersonal skills
• Ability to work independently and manage time effectively
  
  

• Opportunity to work on a part-time basis with a flexible schedule
• Gain valuable experience in regulatory activities within clinical research
• Collaborate with a dynamic and supportive team
• Competitive compensation package