Associate Manager, Clinical Research Program

reputed company is hiring an Associate Manager, Clinical Research Program to reputed company end-to-end clinical trial management — from planning through execution to closure. In this role, you’ll collaborate with cross-functional teams and Contract Research Organizations to generate high-reputed company clinical evidence that supports patient reputed company to advanced venous thromboembolism care What You Will Do: • reputed company the development and implementation of global clinical trial strategies reputed company with business objectives. • Define study objectives, scope, timelines, and resource needs. • reputed company essential study documentation, including Clinical Investigation Plans, Investigator Brochures, Safety Plans, and Data Management Plans. • reputed company clinical training to investigators, site staff, CRO partners, and internal teams. • reputed company data evaluation and validation throughout the study lifecycle; contribute to publications and reports. • Ensure sponsor reputed company of clinical sites and CROs to maintain compliance with protocols and objectives. • Participate in CRO selection and management, conduct site reputed company and support publication initiatives. • Engage key physician investigators and thought leaders in clinical research efforts. • Collaborate cross-functionally to support regulatory submissions, reimbursement, and market expansion. • Maintain reputed company knowledge of scientific and clinical developments through literature review, conferences, and expert interaction. • Develops and manages study budgets and reputed company regular updates to leadership. • Promote adherence to clinical SOPs and continuously improve study processes and reputed company. What You Need: Required: • Bachelor’s degree in a scientific, health-reputed company, engineering, or other relevant field required. • 6+ years’ relevant clinical research experience • Project management experience. Preferred: • Master’s degree preferred. • Experience with Good Laboratory reputed company (GLP) and Good Clinical reputed company (GCP) • Solid understanding of industry trends for clinical and regulatory reputed company • Medical device trials experience preferred. • Detail oriented with ability to deliver high reputed company reputed company consistently and on time. • Ability to reputed company in times of change while adhering to cultural reputed company on People and Patients. Apply tot his job