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Principal Clinical Data Manager (part-time)

Job Type
Location
USA
Salary
US$85 - US$90 per hour
Job Ref
BBBH2310208_1732636592
Date Added
November 26th, 2024
Consultant
tyler rostad

SRG, the leader in the Life Sciences human capital industry, is looking for a part-time Contract Principal Clinical Data Manager for a CRO located in the U.S.

The Principal Clinical Data Manager (PCDM) will have excellent attention to detail and is responsible for overseeing the start-up and execution of several trials to ensure data quality and integrity. PCDMs will independently oversee and/or lead multiple and complex studies within a project and/or program. The individual will perform a variety of complex tasks to ensure complete, accurate, high-quality, and regulatory-compliant data is being delivered. The individual will help manage project and/or program dashboards, closely monitor study metrics, manage study budgets and review the scope of work and overall end-to-end delivery of Data Management services. The individual may also lead governance calls with clients and vendors.

This is a direct, hands-on role and the main requirement is to oversee, as well as manage, all day-to-day Data Management activities. Other responsibilities include, but are not limited to:

  • Oversight management of assigned trials ensuring all tasks are completed withquality, accuracy, completeness and per agreed-upon timelines.
  • Streamline data management processes and provide expertise and support to internal project teams, clients and Clinical Research Organizations (CROs).
  • Serve as primary data management escalation point of contact for issue resolution.

WHAT YOU NEED TO HAVE:

  • 10+ years Data Management experience and B.S./B.A. in a science or technical discipline degree.
  • Previous CRO experience is strongly recommended.
  • Experience in the oversight of large, global projects and working closely with a team of Sr. DMs and supporting staff.
  • Proficient in MS Excel.
  • Ability to program in SQL or SAS desirable, but not required.
  • Experience with various data collection and Electronic Data Capture (EDC) systems and related tools and processes. Medidata Rave EDC, Medrio eClinical and Clario EDC experience are preferred, but not required.
  • Excellent oral and written communication skills.
  • Ability to work in a collaborative and multi-disciplinary environment.
  • Attention to detail, ability to prioritize and manage multiple projects with competing and aggressive timelines.

** "SRG values your application, our team will be in touch to schedule interviews with candidates moving forward in the process."

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.

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