Research Engineer I

Overview

On Site
$40 - $40 hr
Contract - Independent
Contract - W2
Contract - 7+ mo(s)

Skills

Visualization
Communication
Strategic Planning
Records Management
Regulatory Compliance
Documentation
QMS
Forms
Storage
Clinical Trials
Budget
Management
Training
Quality Control
Life Sciences
Medical Devices
Pharmaceutics
Google Cloud Platform
Google Cloud
Research
Project Management
PMP
Clinical Research
Insurance
Privacy
Sourcing
Decision-making
Artificial Intelligence

Job Details

Payrate: $40.00 - $40.00/hr.

Summary:
The Clinical Research Project Manager (Research Program Integrator RPI) is responsible for leading and managing defined research activities for the Advanced Visualization Solutions (AVS) business. This role oversees cross-functional planning, execution, and communication to ensure timely, high-quality, and compliant delivery of research projects. The RPI manages the full lifecycle of research initiatives from strategic planning through execution and closure while meeting all quality, content, schedule, and budget targets.

Roles and Responsibilities:
  • Manage internal and external research activities, including GEHC and Investigator-Sponsored Studies, product evaluations, reader studies, and other strategic research initiatives.
  • Lead cross-functional teams to execute research projects in alignment with business needs and study plans.
  • Partner with the Research Manager (RM) to prioritize and adjust study details as needed.
  • Compliance & Documentation
  • Ensure all research activities comply with cross-functional standards, Phased Review Discipline, QMS, SOPs, Google Cloud Platform, and applicable regional regulatory requirements.
  • Develop and manage essential research documents, including protocols, study plans, informed consent forms, and document storage.
  • Maintain accurate and timely study records in systems such as Clinical Trials Management System, My Workshop, ClinicalTrials.gov, Support Central, and others.
  • Stakeholder & Site Management
  • Negotiate budgets and contracts with external partners and manage payment processes.
  • Conduct or coordinate training, site initiation, monitoring, and study closure activities.
  • Serve as a quality control reviewer for peer studies, supporting review and approval of study activities.
  • Build and maintain professional, productive relationships with external research partners and study sites.

Required Qualifications:
  • Bachelor s degree in life sciences, engineering, clinical field, or equivalent.
  • Demonstrated progressive experience in project management of clinical or technical research in a clinical setting, industry, government agency, or a similar role in a medical device or pharmaceutical company.
  • Strong understanding of Good Clinical Practices (Google Cloud Platform) and global/regional research or device regulations.
  • Proven ability to build and sustain cross-functional relationships.
  • Desired Characteristics
  • Master s degree in a scientific or related field, or an advanced medical degree.
  • Professional certification in project management (e.g., PMP) or clinical research (e.g., CCRP, CCRA, CCRN).


Pay Transparency: The typical base pay for this role across the U.S. is: $40.00 - $40.00/hr. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance.

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