Clinical Research Associate (Clinical Trial) - Remote

Job Description

Job Description

Position: Clinical Research Associate
Location: Remote Role - must be willing to come onsite occasionally at San Diego, CA, 92123
Client: Leading Medical Devices Manufacturer
Duration: 6 months contract
Payrate: $35 - $45/hour

Role Purpose
This role supports the Medical Affairs team during a maternity leave coverage. The team is focused on clinical trials and evidence generation for innovative health technologies beyond traditional sleep apnea solutions, including insomnia and neurostimulation.
Key Responsibilities

• Clinical Trial Support:
  • Site coordination (equipment, documentation, queries)
  • Trial monitoring for data accuracy and compliance
  • Occasional travel for site setup/training (minimal expected)
• Documentation & Organization:
  • Maintain master files, smart sheets, and trial records
  • Ensure proper filing and traceability
• Patient Registry Management:
  • Oversee ResMed’s clinical trial registry (focus on insomnia patients)
  • Support recruitment campaigns and participant data management
  • Coordinate simple studies (e.g., surveys, equipment mailing)
• Patient Interaction:
  • Communicate with trial participants in a professional and personable manner

Job Description:

The primary role of Clinical Studies and Development is the oversight, administration, and execution of the approved clinical study plan. This will include all aspects of the execution of the study, such as contracting, documentation, site visits, and report writing. This role may be as a Study Manager, Clinical Trials Associate, or other similar role.

Let’s talk about Responsibilities

• The primary objective of Clinical Research (CSD) specialization within Clinical Studies & Development Job Family is to oversee and develop clinical projects including research studies in relation to product development.
• Provides strategic input and development support for clinical plans and individual study protocols.
• Participates in the development of clinical operating guides and maintains secure study files.
• Reviews results of these studies with appropriate management prior to publication.
• Demonstrates appropriate technical proficiency, scientific creativity, collaboration with others and independent thought.
• .
• Performs work in a specialized area of expertise that requires knowledge of fundamental themes, principles and concepts. Typically requires a university degree or equivalent work experience.
• Responsibilities might include:
• (1) Performing routine professional-based activities (early in career)
• (2) Contributing to and managing projects (mid-career)
• (3) Providing advice/direction in primary areas of expertise (specialist and expert)
• (4) Leveraging professional expertise and relationships to contribute to strategy and drive business results (principal)relationships to contribute to strategy and drive business results (principal)
• Builds stable working relationships internally to exchange information.
• Receives instruction, guidance and direction from others.

Let’s talk about Qualifications and Experience

Required:

Preferred:

• Bachelor’s degree.
• Minimum of 2 years of related experience.
• Follows standard practices and procedures and applies basic theories, concepts, principles and methodologies in analyzing situations or data.

Company DescriptionDella Infotech Inc is in the staffing business for 10 years. Over the years, we have placed hundreds of candidates to various temp and permanent positions with our 50+ happy clients all over US and Canada including Fortune 500 corporations.

Company Description

Della Infotech Inc is in the staffing business for 10 years. Over the years, we have placed hundreds of candidates to various temp and permanent positions with our 50+ happy clients all over US and Canada including Fortune 500 corporations.