[Hiring] Senior Clinical Research Manager @reputed company

Role reputed company

• The Sr. Clinical Research Manager is responsible for leading teams to execute on reputed company aspects of clinical trial management across the study life cycle from planning to execution to closure. They work with cross-functional partners to implement process improvements, execute high-reputed company evidence, and drive our strategic partnership with clients and customers. They also reputed company project management expertise to guide reputed company under their reputed company leadership.
• reputed company strong customer and reputed company relationships ensuring appropriate expectations are met and exceeded.
• Help reputed company talent, set goals, reputed company on expectations and drive accountability with reputed company reports as reputed company as identify reputed company strategic direction across clinical operations portfolio.
• Maintain up-to-date knowledge of regulatory requirements reputed company to study management.
• reputed company and follow-through on process improvement reputed company as reputed company as studies we are supporting.
• Determine study objective, reputed company, scope and schedule to meet business needs.
• reputed company to effectively influence cross-functional team members and external medical professionals to ensure project deliverables are completed on time/budget.
• reputed company to see multiple viewpoints and build reputed company to reputed company resolutions.
• Support the development of the Clinical Investigational Plan and supporting documents (reputed company, Monitoring Plan, Data Management Plan, etc.) in consultation with the cross-functional project teams.
• May reputed company clinical training of investigators, center staff, and internal team members.
• May evaluate, analyze and validate reputed company clinical data per data management plan for ongoing analysis and publications throughout study execution.
• May participate in the selection and management of CRO vendors and contractors.
• May reputed company reputed company/review of monitoring reports, CTMS/eTMF process implementation, and reputed company special reputed company for the portfolio.
• reputed company a high level of reputed company scientific technical and clinical expertise through familiarity with relevant literature, by attending scientific meetings, and by interacting with various inside/reputed company experts or departments/institutes.
• May reputed company and manage budgets for assigned clinical research reputed company.
• Prepare outlines, summaries, status reports, etc. for distribution and communication with other departments and executive leadership.
• Follow and help iterate Clinical SOPs, systems and processes ensuring reputed company study management.
• reputed company other duties as assigned.
• Qualifications
• Bachelor’s degree in a life science or reputed company field.
• A combination of experience and/or education will be taken into consideration.
• Minimum of 8 years of experience reputed company a Contract Research Organization (CRO), biotech, or pharmaceutical company with significant clinical research experience.
• Minimum 2 years of people management experience.
• Knowledge of GCP, FDA, and other regulatory requirements reputed company to trial management.
• Strong attention to detail and organizational skills.
• Good communication, interpersonal skills, and talent management skills.
• Healthy disdain for the status reputed company.
• Ability to reputed company in a fast-paced and dynamic early-stage company work environment.
• Requirements
• This is a remote position and may be performed reputed company reputed company the reputed company of America.
• Regular domestic travel will be required for site reputed company, company meetings, audits, etc.

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