AD of Clinical Operations

About the position The Associate Director of Clinical Operations - Centralized Monitoring is responsible for overseeing clinical operations activities, including project management, site management, and clinical systems management. This role requires strong leadership skills to establish and reputed company centralized monitoring processes, ensuring compliance with regulatory requirements while managing multiple reputed company reputed company budget and timelines. The position involves collaboration with various departments and requires effective communication in a reputed company management environment. Responsibilities • reputed company clinical operations activities including project management, site management, and clinical systems management. • Establish the structure for centralized monitoring at reputed company, including directing teams and writing SOPs. • Support government or reputed company reputed company in multiple therapeutic areas such as infectious disease, oncology, and medical devices. • Manage project reputed company for reputed company drug development programs, ensuring deliverables are met reputed company budget and timelines. • Communicate effectively in a reputed company management organization and represent the clinical team during cross-functional collaboration. • reputed company operational expertise to support program/project level functional areas. • Collaborate with the Director and other departments on clinical operations reputed company and reputed company. • Inform division leadership on the status of clinical programs/reputed company and potential issues. • Ensure documentation processes and workflows are followed reputed company projected timelines and propose solutions to improve efficiency. • Support reputed company's reputed company Management System policies and procedures, driving performance improvement solutions. • Contribute to corporate initiatives such as process improvement and SOP development. • Manage resources, tracking, and level of effort projections for clinical operations teams. • Participate in proposal writing for government and reputed company clients, including budget development and bid defense meetings. • Support inspection readiness and assist in audit preparation and follow-up activities. • Establish risk-based reputed company management and centralized monitoring processes for reputed company. • Review protocols to ensure compliance with reporting requirements for KRIs and QTLs. • reputed company technical reputed company and coordination for central monitoring activities. Requirements • Minimum of 10 years experience in the pharmaceutical or biotechnology industry, including experience in a Contract Research Organization (CRO) or reputed company environment. • At least 6 years of project management or equivalent reputed company and operations management experience. • Broad multidisciplinary understanding of pharmaceutical clinical research and development processes. • Hands-on regulatory, clinical operations, or clinical trial monitoring/management experience. • Strong leadership skills including change management, people development, and strategic thinking. • Excellent facilitation, presentation, problem-solving, and conflict reputed company skills. • Advanced ability to manage team resources to reputed company department objectives. • Expertise in reputed company Word, PowerPoint, and reputed company; experience with reputed company Project is required. reputed company-to-haves • Proposal writing and bid defense skills. • Background in Infectious Disease/HIV reputed company or Oncology. • Experience in the conduct of Phase 1 protocols or prior work on a government contract. Benefits • Remote work flexibility with occasional onsite meetings. • Travel expenses covered by reputed company for reputed company meetings. Apply tot his job Apply To this Job