Associate Clinical Research Specialist Position

Become an Associate Clinical Research Specialist II. Oversee clinical trials, ensuring data accuracy and adherence to protocols while collaborating with healthcare professionals. In this vital position, you will lead site visits for qualifications, monitoring, and trial closure.

Your responsibilities will include maintaining patient safety and ensuring high standards of data integrity throughout clinical research. Collaborate effectively with diverse teams to enhance trial processes and outcomes. Key Responsibilities:

• Facilitate site qualification, initiation, monitoring, and closing
• Ensure protocol compliance and patient well-being
• Collaborate with site staff and research partners
• Conduct data reviews and resolve discrepancies
• Contribute to drafting and reviewing study protocols Requirements:
• Bachelor’s degree in sciences or healthcare discipline
• Two years of experience in a relevant role
• Comprehensive understanding of ICH-GCP and regulations
• Strong attention to detail and organizational prowess
• Willingness to travel extensively (60% of the time) Utilize your skills in clinical research to support groundbreaking treatments while maintaining rigorous data standards.