Clinical Research Associate

Job Description

We are seeking a dedicated Clinical Research Associate to join our dynamic team in London. The successful candidate will play a pivotal role in overseeing clinical trials, ensuring compliance with regulatory requirements, and coordinating with healthcare professionals to facilitate research studies.

Responsibilities

• Manage communications with regulatory bodies and ethics committees.
• Identify and resolve issues that arise during the course of clinical trials.
• Participate in strategic planning and implementation of clinical research activities.
• Assist in the analysis of clinical trial data and reporting outcomes.
• Maintain study files in compliance with regulatory standards.

Requirements

Education

• Bachelor's in Pharmacy or a related medical field
• Advanced degree (MSc or PhD) desirable

Experience

• 3+ years of experience in clinical trials management

Technical Skills

• Study Protocol Development
• Patient Management
• Clinical Data Management Systems

Soft Skills

• Teamwork
• Attention to Detail

Certifications

• Clinical Research Associate (CRA) Certification

Languages

• English: Fluent

Advantageous

• Background in pharmacovigilance: Experience in monitoring the safety of clinical trial participants.
• Knowledge of therapeutic areas: Understanding of specific therapeutic areas such as oncology or cardiology.

Benefits

• Comprehensive health insurance
• Generous annual leave
• Professional development support
• Work-life balance initiatives

Company Culture

• Continuous Learning: Our team is committed to professional growth and continuous learning.
• Supportive Environment: We provide a supportive environment where every voice is valued.