Clinical Research Associate

Barrington James; Palma de Mallorca; Presencial; EUR 30.000 - 50.000; A tiempo parcial

Descripción de la vacante

A respected sponsor company is seeking a Clinical Research Associate for a part-time freelance position in Spain. The role involves overseeing regulatory compliance for clinical trials, coordinating with authorities, and conducting site visits. Ideal candidates will have a scientific degree and proven experience in regulatory activities, along with strong communication skills.

Servicios

Flexible schedule

Competitive compensation package

Opportunity to gain valuable experience

Collaboration with a supportive team

Formación

• 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.

Responsabilidades

• Oversee regulatory compliance for clinical trials.
• Coordinate with regulatory authorities and ethics committees.
• Conduct site visits to assess regulatory compliance.

Conocimientos

Regulatory compliance

Communication

Interpersonal skills

Time management

Educación

Bachelor's degree in a scientific or healthcare discipline

Descripción del empleo

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

Qualifications

• 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

Day-to-Day

As a Clinical Research Associate, you will be responsible for ensuring regulatory compliance throughout the lifecycle of clinical trials. This will involve liaising with regulatory authorities, conducting site visits, and maintaining accurate documentation to support regulatory submissions.

• 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

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