RWE Sr. Site Manager 2 with Spanish or French

PURPOSE
Responsible for independently and effectively managing sites to drive their performance throughout the lifecycle of the study, from site identification to study closure. Act as single point of contact with sites and ensure compliance with all applicable regulations, Good Clinical Practices (GCP), and standard operating procedures (SOPs).

RESPONSIBILITIES

• Perform site identification and selection, start-up, initiation, monitoring and close out in accordance with contracted scope of work, using good clinical practices applicable regulations, SOPs and work instructions
• Act as single point of contact with study sites, ensuring successful collaboration and meeting study expectations and milestones
• Prepare ethics submissions and negotiate site contracts and budgets
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
• Conducts continuous monitoring activities (both onsite and remote)
• Identifies issues at sites; resolves issues and escalates as appropriate
• Execute assigned work efficiently and adhere to project timelines and financial goals; review site performance metrics and make recommendations accordingly
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters, essential document collection and filing and other required study documentation
• May conduct primary data collection at sites
• May aid less experienced staff, including demonstrating appropriate interactions with sites, documentation and other monitoring activities. May act as point of contact for other staff on project

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

• Strong knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Strong command of English and Spanish (both C1 level) or English and French (both C1 level)
• Ability to anticipate potential issues and take appropriate actions with and/or without supervision
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
• Advanced communication skills and ability to influence others
• Ability to manage multiple priorities and manage time efficiently
• Ability to travel domestically (possibly internationally) as needed to study sites and meetings
• Occasional overnight travel may be required

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

• Bachelor’s Degree, preferably in life science, and > 4 years of site monitoring and management experience; or equivalent combination of education, training and experience 

PHYSICAL REQUIREMENTS

• Extensive use of telephone and face to face communication requiring accurate perception of speech
• Extensive use of keyboard requiring repetitive motion of fingers
• Regular sitting for extended periods of time

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.