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Clinical Data Manager (Temporary Position, 20 hours/week)Penumbra, Inc. · Your Remote US Home Office
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Penumbra, Inc.

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Clinical Data Manager (Temporary Position, 20 hours/week)

🗓️ Posted 2026-10-20 Your Remote US Home Office Temporary Hybrid Science Technology
💰 Salary US$50–US$80/mo (US$600–US$960/yr) 📊 Market US$2,400–US$3,600/mo

About the Company

General Summary The temporary Clinical Data Manager acts as a lead data manager for one or more projects, applies data management experience to clinical trials, and utilizes functional knowledge of the logistics of clinical trials to ensure the quality and integrity of clinical trial data. The CDM works on multi-functional teams and supports clinical trial projects as a departmental subject matter expert (SME). We are seeking a temporary clinical data manager who can dedicate 20 hours a week to support ongoing study activities. The initial assignment is for 6 months, but may be extended to meet the needs of our Team. Applicants must be eligible to live and work in the US. Specific Duties and Responsibilities Independently lead and/or perform all data management activities within an assigned study (e.g., study startup, study conduct, study closeout, and reporting). Serve as the data management SME on multidisciplinary project teams providing specific expertise on timeline development, identification of data management deliverables and resource requirements. Participate in the creation, review, and maintenance of project timelines and monitor progress of data management activities. Provide oversight for Data Management CRO and other vendors to ensure compliance with the protocol, external/internal standards, Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, and other relevant guidelines. Ensure Data Management documentation is filed/archived ac

Requirements

  • ● Master's degree with 3+ years of clinical research, pharmaceutical company preferred
  • ● Thorough knowledge of effective clinical data management practices; CCDM certified professional a plus
  • ● This position must have experience working on regulatory trials within the medical device and/or pharmaceutical industry
  • ● Position requires technical, organizational, analytical, and strong communication skills
  • ● Knowledge of regulatory guidelines pertaining to data quality and data management
  • ● Proven experience and in-depth understanding of all aspects of Data Management
  • ● Ability to effectively manage change and multiple priorities
  • ● Ability to operate independently and achieve results; ability to effectively deal with employees and business contacts and conveys a positive service-oriented attitude
  • ● Knowledge of continuous improvement, project management, change management, and risk management
  • ● Medical device, pharmaceutical, biotech, or other regulated industry experience required
  • ● Proficiency with MS Word, Excel, and PowerPoint
  • ● Working Conditions
  • ● General office environment
  • ● Willingness and ability to work on site.
  • ● May have business travel from 0% - 5% to conferences and/or other Penumbra affiliated facilities.
  • ● Potential exposure to blood-borne pathogens
  • ● Requires some lifting and moving of up to 25 pounds
  • ● Must be able to move between buildings and floors.
  • ● Must be able to remain stationary and use a computer or other standard office equipment, such as a printer or copy machine, for an extensive period of time each day.
  • ● Must be able to read, prepare emails, and produce documents and spreadsheets.