Clinical Research Associate

We're partnering with a Pharmaceutical MNC in the search for an Assistant Clinical Research Manager (candidates with less experience will be considered as a Clinical Research Associate).

Responsibilities

• Develops and maintains strong relationships with clinical trial sites throughout all phases of the trial
• Ensures compliance with relevant regulations, protocols, and standard operating procedures during site management and monitoring activities
• Supports site selection and validation processes, providing input and coordination
• Conducts thorough monitoring and oversight activities, ensuring data integrity and subject safety
• Collaborates with various stakeholders, both internally and externally, to address site performance, quality, and compliance issues and contribute to the development of new research sites

Requirements

• Min. 2 years of direct site management (monitoring) experience in a BioTech/Pharma/CRO companies
• Bachelor's degree in life science related degrees
• Strong communication skills, including fluency in local languages and English, with the ability to effectively present technical information
• Comprehensive understanding of clinical research, including knowledge of current GCP/ICH guidelines and local clinical research laws
• Proficiency in site management, including patient recruitment and performance management
• Ability to work independently across multiple protocols, sites, and therapy areas, demonstrating accountability and the ability to prioritize tasks
• Excellent organizational skills, problem-solving abilities, and a commitment to quality and compliance, with a positive and growth-oriented mindset