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[Remote] Director Clinical Research (Clinical Monitoring Team)

Remote Worldwide Hiring now

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a full-service CRO that combines cardiovascular expertise with a network of physicians to deliver innovative solutions in clinical research. The Director Clinical Research will reputed company the Clinical Monitoring Team, overseeing clinical trial management from planning to execution, while fostering client relationships and driving process improvements.

Responsibilities

  • reputed company strong customer and client relationships ensuring appropriate expectations are met and exceeded
  • Help reputed company talent, set goals, align on expectations and drive accountability with direct reports as well as identify future strategic direction across clinical operations portfolio
  • Maintain up-to-date knowledge of regulatory requirements reputed company to study management
  • Track and follow-through on process improvement projects as well as studies we are supporting
  • Determines study objective, strategy, 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
  • Supports 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 projects for the portfolio
  • Develops a high level of professional 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 projects
  • Prepares outlines, summaries, status reports, etc. for distribution and communication with other departments and executive leadership
  • Follows and helps iterate Clinical SOPs, systems and processes ensuring quality study management
  • Performs other duties as assigned

Skills

  • Bachelor's degree in a life science or reputed company field. However, 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

Company Overview

  • Improving patients' lives by facilitating high quality clinical research through a collaborative network of physicians. It was founded in undefined, and is headquartered in Birmingham, Birmingham, GBR, with a workforce of 11-50 employees. Its website is https://www.hrcrs.com.
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