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Principal Clinical Data Manager job in London at CLINIPACE

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Principal Clinical Data Manager at CLINIPACE

Principal Clinical Data Manager

CLINIPACE London, Greater London Full Time

Job Duties and Responsibilities:

The specific job duties of a Principal Clinical Data Manager may include but are not limited to:

  • Lead all activities for complex global clinical trials
  • Coordinate the work of global staff assigned to the project
  • Provide training on procedures and systems
  • Create project-related materials
  • Track project progress and issue status reports
  • Develop and maintain communication with colleagues in other departments
  • Ensure the achievement of key milestones relating to the function, such as completion of tasks towards final database
  • Attend sponsor related meetings
  • Participate in business development meetings
  • Serve as the principal function specialist for the department for assigned projects
  • Assist in the creation and documentation of new or revised departmental procedures and guidelines
  • Supports and tracks budget adherence in cooperation with Finance to ensure the assigned studies are meeting targeted margins and utilization
  • Contributes to the departmental strategy and goals, working closely with the DM Lead team to ensure alignment with overall Corporate strategy and goals
  • Continuous process improvement of departmental processes and procedures to ensure DM is consistently maximizing efficiencies, leveraging technology and incorporating innovation to optimize delivery
  • Maintains working knowledge of regulatory requirements/guidance as well as industry leading best practices to ensure Clinipace DM procedures are in line with industry expectations
  • May participate in interviewing potential new department team members
  • May participate in or lead process improvement initiatives
  • May indirectly supervise others, as needed
  • The Principal Clinical Data Manager serves as a leader in project team activities.
  • Other duties as assigned
  • Supervisory Responsibilities:

    No supervisory responsibilities.

    Job Requirements:

  • Education College graduate with a degree in life science, computing or nursing qualifications required or equivalent combination of education and experience.
  • Experience 10 + years practical clinical trials experience Minimum of 10 years of experience and/or demonstrated aptitude for data management work and managerial skills Global team leadership skills Experience working in the Contract Research Organization (CRO) industry (pharma industry tenure could be considered) Expertise in clinical development lifecycle and interdependencies of data management Expert knowledge of EDC studies and ancillary data Cross functional meeting attendance and leadership
  • Skills/Competencies Excellent organizational skills Strong written and verbal communication skills Exceptional attention to detail Knowledge of clinical research including regulatory requirements GCP/ICH Proficiency in industry standard data management systems (e.g., RAVE, Medrio, etc.) Strong interpersonal skills; serve as the primary company liaison for data management issues Able to exercise judgment within defined procedures and practices and to determine appropriate action independently Decision making, planning and delegation skills Mature management skills demonstrated by calm and thorough review of situations
  • Capabilities Flexibility - willing to change assignments and work focus to accommodate project demands Data driven, evidence based work ethic leveraging tools, reports and other knowledge information sources to drive efficiency in data management activities Team player: effective proactive participant as a team member and team leader Dedicated home office environment for home-based employees, as applicable Travel: Some local and international travel may be required
  • The company does not accept unsolicited resumes from third party vendors.


    Recommended Skills

    • Leadership
    • Hardworking And Dedicated
    • Attention To Detail
    • Decision Making
    • Coordinating
    • Clinical Research
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    Job ID: 0290a98dc7d2