Senior Clinical Data Manager – strong oncology experience

Data ScientistData ScientistFull TimeRemoteTeam 10,001+H1B No SponsorCompany SiteLinkedIn

Location

United States

Posted

67 days ago

Salary

Not specified

Bachelor Degree8 yrs expEnglish

Job Description

• Provides CDM leadership for one or more assigned projects or indications dependent on size and scale of the project • Lead studies including (but not limited to) a combination of healthy volunteer and patient populations, multi-site, complex protocol design, strong client management required or reduced timelines • Demonstrates leadership and operational expertise in the strategic planning and delivery of CDM deliverables at program and/or project level • Management and oversight of vendor contracts, resourcing and budget management and oversight of vendor performance for assigned programs, and projects • Communicates and negotiates effectively with all other Program level team members • Primary point of contact for Clinical Data Management (CDM) • Provide oversight and expertise of external service providers or in-house teams to deliver quality data with compliance to study model procedures and standards; Responsible for proactive risk management and issue resolution/escalation connected to Clinical Data Management improvement or technology • Develops an understanding of CDASH and SDTM or other recognized industry standards and impact to programming team to ensure consistency of program level standards

Job Requirements

  • University/college degree (life science, pharmacy or related subject preferred)
  • 8 years of combined early or late-stage DM experience with minimum 2 years of direct sponsor management and at least 2 years technical mentoring experience
  • Extensive experience in clinical data management
  • Experience leading studies in a CRO/Pharma setting
  • Understanding of RECIST criteria
  • Excellent oral and written communication and presentation skills
  • In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations
  • Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies

Benefits

  • Highly competitive compensation packages, including various local benefits such as pension contributions
  • Complimentary health insurance plans
  • Remote working allowances
  • Genuine work life balance
  • Flexibility in working hours
  • A thorough onboarding with support from your personal mentor

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