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Full-Time

Technical Project Manager I

Posted on 2/21/2024

YPrime

YPrime

201-500 employees

eClinical platform for clinical trial management

Data & Analytics

Junior, Mid

Malvern, PA, USA

Category
Project Management
Strategy Development
Business & Strategy
Required Skills
SQL
Requirements
  • Bachelor's degree in related field or equivalent experience
  • Minimum of 3 years' experience in IRT
  • Minimum of 3 years' project management experience
  • Experience with software systems in support of clinical trials
  • The ability to travel up to 20% of the time
  • Foundational knowledge of the principals of the Software Development Life Cycle
  • Proficiency in Microsoft Office applications
  • Project or Product Management-related certification (PMP, CAPM, PgMP, etc.)
  • Experience with SQL (querying databases)
  • Experience with SaaS delivery
  • Experience with Scrum Software Development
  • Experience in biotech/pharmaceutical or the CRO industry
Responsibilities
  • Ensure all requirements for system build are identified, documented, and communicated across the project team
  • Provide consistent implementation of Software Development Life Cycle
  • Responsible for the technical design of basic studies based on protocol, client requests and experience
  • Review and support configuration of basic systems
  • Ensure all functional requirements are captured in Systems Requirements Document and other applicable system requirements documents
  • Translate functional requirements into technical specifications for programmers
  • Lead the team in ad-hoc testing of requirements in the development environment
  • Ensure the delivery of a clean study through validation environment
  • Support system validation through the timely triaging of defects
  • Demonstrate software prototypes for customers
  • Set and track project milestones related to technical delivery; manage and account for unforeseen delays and realign schedules and expectations as needed

YPrime specializes in eClinical solutions such as eCOA, eConsent, and IRT, which streamline data management in clinical trials using advanced technology. This focus on enhancing efficiency and data quality, while easing the burdens for participants, creates a dynamic work environment tailored for innovation in clinical technology. There, employees can contribute to significant advancements in healthcare processes, elevating their professional skills while working toward global health improvements.

Company Stage

Seed

Total Funding

$10M

Headquarters

Malvern, Pennsylvania

Founded

2006

INACTIVE