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Remote Biomedical Research Assistant Jobs in Puerto Rico

Tetra Tech

Urban Planning Specialist - Ponce, PR

Ponce, PR · On-site +1

$65K - $85K/yr

Working under the direction of the Senior Urban Planning Lead, this position will assist in the ... Conduct research on vacant property management, neighborhood revitalization, and planning best ...

Tetra Tech

Urban Planning Specialist - Ponce, PR

Ponce, PR · On-site +1

$65K - $85K/yr

Working under the direction of the Senior Urban Planning Lead, this position will assist in the ... Conduct research on vacant property management, neighborhood revitalization, and planning best ...

All JobsBiomedical Research JobsRemote Biomedical Research Assistant JobsRemote Biomedical Research Assistant Jobs in Puerto Rico

Remote Biomedical Research Assistant information

What is a Remote Biomedical Research Assistant?

A Remote Biomedical Research Assistant is a professional who supports biomedical research projects from a remote or off-site location. Their responsibilities typically include data collection and analysis, literature reviews, preparing research reports, and assisting with experiment coordination. They work closely with research teams, often using digital communication and project management tools. This role allows individuals to contribute to advancements in medical science without being physically present in a laboratory or research facility.

How does a remote biomedical research assistant typically collaborate with laboratory teams and principal investigators?

As a remote biomedical research assistant, collaboration is primarily achieved through virtual meetings, cloud-based data sharing, and regular email or chat communication. You’ll often coordinate with laboratory teams to receive experimental data, assist with data analysis, and contribute to writing reports and publications. Building strong communication skills is essential, as you may need to clarify research protocols, troubleshoot issues, and stay aligned with project timelines, all while working from a distance. Many organizations also use project management tools to track tasks and progress, ensuring everyone is informed and connected.

What are the key skills and qualifications needed to thrive as a Remote Biomedical Research Assistant, and why are they important?

To thrive as a Remote Biomedical Research Assistant, you need a solid background in biology or biomedical sciences, experience with data analysis, and often a bachelor's degree in a related field. Familiarity with software like Microsoft Excel, statistical tools such as SPSS or R, and collaborative platforms like Zoom or Slack is typically required. Excellent time management, attention to detail, and proactive communication are essential soft skills for remote teamwork. These skills and qualities ensure accurate research support, effective virtual collaboration, and reliable contribution to ongoing scientific projects.
What job categories do people searching Remote Biomedical Research Assistant jobs in Puerto Rico look for? The top searched job categories for Remote Biomedical Research Assistant jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Remote Biomedical Research Assistant jobs? Cities in Puerto Rico with the most Remote Biomedical Research Assistant job openings:
Remote Biomedical Research Assistant jobs near you
Infographic showing various Remote Biomedical Research Assistant job openings in Puerto Rico as of July 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution.
Sterilization Program Manager- Ethylene Oxide (EO) (Remote Work)

Sterilization Program Manager- Ethylene Oxide (EO) (Remote Work)

CIS International LLC

Juncos, PR • On-site, Remote

Full-time

Posted 4 days ago

Job description

Summary:
The Sterilization Program Manager is responsible for leading and managing the sterilization project portfolio, including new product launches, validation and revalidation activities, process improvements, and operational support. This role provides technical oversight for Ethylene Oxide (EO) sterilization processes, drives cross-functional collaboration, manages supplier relationships, and ensures compliance with global sterilization regulations and standards.
Key Responsibilities:
Program & Portfolio Management
  • Lead and manage the full sterilization project portfolio, including:
    • New product launches
    • Sterilization validations and revalidations
    • Process improvement initiatives
  • Develop and maintain integrated project plans, timelines, resource allocation plans, and risk registers.
  • Drive alignment across cross-functional teams including R&D, Quality, Regulatory Affairs, Operations, and Supply Chain.
  • Facilitate portfolio prioritization and support trade-off decisions with senior leadership.
  • Establish, monitor, and report key performance indicators (KPIs), project milestones, and program health metrics.
Technical Oversight
  • Serve as Subject Matter Expert (SME) for EO sterilization processes.
  • Provide technical guidance related to microbiological and chemical sterilization methods.
  • Ensure compliance with applicable international regulations, standards, and industry requirements.
  • Support technical problem-solving and troubleshooting efforts across sterilization-related activities.
  • Collaborate with internal SMEs to resolve complex sterilization challenges.
Sterilization & Service Supplier Management
  • Coordinate with internal stakeholders to manage relationships with contract sterilization providers and laboratory service vendors.
  • Support project scheduling and resource planning with external service suppliers.
  • Ensure supplier activities align with project priorities, timelines, and business objectives.
Stakeholder & Change Management
  • Communicate project status, risks, mitigation plans, and key decisions to executive leadership and cross-functional teams.
  • Lead change control activities associated with sterilization process modifications.
  • Promote continuous improvement initiatives and process optimization opportunities.
  • Drive effective stakeholder engagement throughout the project lifecycle.
Requirements
  • Bachelor’s Degree in:
    • Biomedical Engineering
    • Chemical Engineering
    • Microbiology or related scientific/engineering discipline
  • Minimum 3 years of experience in EO sterilization validation and/or sterilization operations.
  • Strong knowledge of sterilization validation lifecycle activities.
  • Experience supporting validation, compliance, and process improvement projects.
Preferred Qualifications
  • PMP Certification or equivalent project management certification.
  • Experience in medical device, pharmaceutical, or regulated manufacturing environments.
  • Knowledge of international sterilization standards and regulatory requirements.
Required Skills
Sterilization & Validation
  • EO Sterilization Processes
  • Sterilization Validation Lifecycle
  • Revalidation Activities
  • Microbiological Methods
  • Chemical Sterilization Methods
  • Regulatory Compliance
Program Management
  • Portfolio Management
  • Resource Planning
  • Project Scheduling
  • Risk Management
  • FMEA
  • Risk Registers
  • KPI Development & Reporting
  • Cross-Functional Leadership
Software & Tools
  • Microsoft Office Suite
  • Microsoft Project
  • Smartsheet
  • Agile Methodologies
Soft Skills
  • Leadership
  • Strategic Planning
  • Stakeholder Management
  • Communication & Presentation Skills
  • Problem Solving
  • Continuous Improvement Mindset
  • Change Management
Work Methodology
  • Remote work reporting to the Juncos, PR site.
  • Full Time Job 
  • Shift: Administrative Shift, but needs to be available for others.
  • Duration: 1 year (with possible extension or conversion depending on project and performance).
  • Professional services Contract
  • Type of industry: Medical devices