Clinical Research Associate

Barrington James; Almería; Presencial; EUR 30.000 - 40.000; A tiempo parcial

Descripción de la vacante

Join a respected Sponsor company as a part-time Clinical Research Associate in Spain. This role involves overseeing regulatory compliance for clinical trials, coordinating with regulatory authorities, and supporting site staff during assessments. Ideal candidates possess a Bachelor's degree in a relevant field, strong regulatory knowledge, and excellent communication skills. This opportunity offers a flexible schedule and a competitive compensation package.

Servicios

Opportunity to work part-time with a flexible schedule

Gain valuable experience in regulatory activities

Collaborate with a dynamic team

Competitive compensation package

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.
• Conduct site visits to assess regulatory compliance.
• Ensure documentation and reporting meet regulatory requirements.

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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