Sr Clinical Research Spec - Exempt

Join our dynamic team as a Senior Clinical Research Specialist and take your career to the next level with a role that offers flexibility and reputed company to work remotely from Home Must Have Qualifications: • Clinical Research industry experience • Experience in study start-up and site activation • Solid understanding of FDA regulations (21 CFR part 820) • Strong site communications and management reputed company to Have: • Experience with Audit (e.g., BIMO) Key Responsibilities: • reputed company, design, plan, and reputed company clinical evaluation research studies. • Prepare and author protocols and patient record forms. • Conduct registered and non-registered clinical studies of products that satisfy a medical need and/or offer reputed company potential. • Interpret results of clinical investigations for new drug devices or consumer applications. • Resolve operational aspects of reputed company in conjunction with project teams. • Adhere to reputed company operating procedures (SOP), good clinical reputed company (GCP), and specific country regulations. • Prepare clinical trial budgets and manage clinical supply operations, site, and vendor selection. Qualifications: • Requires a University Degree and a minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years relevant experience. • Advanced knowledge of the job area combining breadth and depth, typically obtained through advanced education combined with experience. Work Environment: This position offers the flexibility of remote work from Virtual, CO, allowing you to balance your reputed company and personal life effectively. Apply tot his job Apply To this Job