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Trial Specialist
Nrdg
Posted on 7/18/2022
INACTIVE
Locations
Princeton, NJ, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Google Cloud Platform
Leadership
Management
Research
PowerPoint/Keynote/Slides
Word/Pages/Docs
Requirements
  • BA/BS or associates degree in relevant discipline
  • 1-3 years' experience in Clinical Research or related work experience. Experience in the use of industry Clinical Trial Management Systems and Clinical Trial Master File Systems
  • Basic knowledge of clinical research budgets including processing and tracking of site and vendor payments is preferred
  • Knowledge of ICH/GCP, regulatory guidelines/directives, and the drug development process
  • Basic understanding of project management desired
  • Proficient in Microsoft Word, Excel and PowerPoint
  • Displays a willingness to challenge the status quo and take risks
  • Effective oral and written communication skills, ability to influence cross-functionally, demonstration of leadership capabilities
Responsibilities
  • Supports successful and timely operational execution of Late Development research (BMS sponsored late phase, non-interventional research (NIS), ISRs, PAA)
  • Supports project management concepts to manage issues, risks, and timelines
  • Leverages interpersonal and influencing skills to foster partnerships across multidisciplinary teams
  • Drives process / system enhancements related to TS responsibilities / deliverables and manage / comply with various quality or compliance systems
  • Focus on local level projects including local country studies
  • Study & Project Planning, Conduct and Management
  • Manages country planning, protocol level attributes and milestones/drivers in CTMS
  • Manages the development and/or collection of study level documentation, support Trial Manager in ensuring eTMF accuracy and completion for all studies
  • Facilitates vendor creation and payment processing in conjunction with the appropriate stakeholders
  • Raises possible issues for potential escalation to the appropriate colleagues
  • Follows instructions, determines level of understanding, and seeks clarification when needed
  • Facilitation of fund management and payments in collaboration with respective stakeholders
  • Ensure payment processing and reconciliation
  • Manage trial documents and data for the Trial Managers within given Hub/Region
  • Cross functional engagement with various Stakeholders
Bristol-Myers Squibb

10,001+ employees

Biopharmaceutical development company
Company mission
Bristol-Myers Squibb engages in the discovery, development, licensing, manufacturing, marketing, distribution and sale of pharmaceuticals.