Join Us as a CM Analyst I– Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than
750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5
years.
As part of our expert team, you’ll have the prospect to ensure operational
excellence that makes a real difference in organizational performance. As a
Trial Data Analytics Specialist II, you will identify and characterize issues
and trends in operational and patient clinical trial data using analytical or
statistical tools. You will leverage your operational experience and knowledge
to evaluate issues and develop findings based on the data analyzed,
communicating issues and potential risks to project team members for follow-up
action.
What You’ll Do:
• Reviews clinical trial data using a variety of tools and systems in alignment
with the centralized monitoring plan with support from senior team members.
• Characterizes and tracks the evidence of issues, signals and potential risks
with support from senior team members.
• Ensures results of reviews are appropriately documented per department
procedures.
• May participate in development of risk characterization and reporting.
• Supports review set-up, including updating department database, pulling
reports, etc.
Education and Experience Requirements:
• Bachelor's degree or equivalent and relevant formal academic / vocational
qualification
• Previous experience that provides the knowledge, skills, and abilities to
perform the job (comparable to 2+ years’). Prior experience in clinical
monitoring, data management, biostatistics or related field in support of
clinical trials is preferred.
In some cases an equivalency, consisting of a combination of appropriate
education, training and/or directly related experience, will be considered
sufficient for an individual to meet the requirement