CURRENT OPENINGS

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Research Clinician
Research clinicians at Parameters Research Laboratory are essential to the safe and effective conduct of study protocols. They take initial and ongoing vital signs, collect physiological measurements, and monitor participants’ health throughout each study visit. They ensure all procedures are performed according to protocol and maintain accurate, detailed documentation of clinical observations. This includes entering data into Electronic Data Capture (EDC) systems as required. They work closely with engineers, statisticians, and research technicians to support study execution and troubleshoot any issues that arise during testing. Typical backgrounds include registered nurses (RN), physician assistants, or other professional medical training relevant to clinical research. This role demands strong clinical judgment, exceptional attention to detail, excellent communication skills, and a commitment to participant safety and study integrity.

• Conduct participant health assessments

• Collect and interpret participant data from source documents, medical records, and health screening forms, ensuring accuracy and completeness

• Determine participant eligibility for enrollment into studies

• Identify potential risks, manage and report adverse events

• Document clinical observations accurately and in detail, maintaining high attention to data integrity.

• Maintain accurate and detailed participant case report forms and regulatory files, ensuring compliance with ethical, legal, and regulatory standards.

• Act as a liaison between the sponsor regarding protocol implementation and participant safety. 

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Research Engineer or Data Analyst
Research engineers and data analysts at Parameters Research Laboratory combine technical expertise with analytical skill to support medical device research from development through validation. They design and refine custom measurement tools, prepare and validate study equipment, and ensure devices meet performance standards. On the analytical side, they manage and process complex datasets — integrating device readings, physiological measurements, and participant data — to produce clean, accurate reports for regulatory submission. They must be able to interpret and execute international standards and comply with requirements from regulatory bodies to ensure study outcomes are accepted globally. Typical backgrounds include biomedical engineering, biomedical science, computer science, data science, or related fields. This role bridges the gap between engineering, data science, and clinical research, ensuring that every study is both technically sound and scientifically rigorous.

Key Responsibilities Include

Clinical Study Support:

• Collaborates with clinical research clinicians, the sponsor, and other team members to design and execute clinical studies.

• Provides data monitoring tools, data analysis tools, and technical support for clinical data management.

• Monitors and analyzes study datasets and signal quality to ensure data integrity and identify discrepancies.

Reports and Regulatory Submissions:

• Prepare technical and analytical reports summarizing study results, device performance, and data trends.

• Compile, review, and organize data for submission to regulatory bodies (e.g., FDA, ISO, CE).

• Support the creation of regulatory documentation, including protocols, validation reports, and CRFs.

• Collaborate with cross-functional teams to verify data accuracy and completeness prior to submission.

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Research Technician
Research technicians at Parameters Research Laboratory provide hands-on support throughout every stage of a study. They set up and monitor devices, collect and record data, and verify that all procedures strictly follow the study protocol. In addition to technical duties, they interact directly with study participants, guiding them through procedures, answering questions, and ensuring comfort and compliance throughout the visit. Working side-by-side with engineers, clinicians, and data teams, they ensure that every measurement is accurate and every step is meticulously documented. This role demands exceptional attention to detail, strong technical skills, and a commitment to maintaining the highest standards of research quality.

Key Responsibilities Include

Data management and documentation:

• Accurately documenting all research activities in participant case report forms and electronic data capture systems.

• Ensuring data integrity and quality control.

• Maintaining and organizing study-related documents.

Compliance and safety:

• Following study protocols and standard operating procedures (SOPs).

• Ensuring adherence to ethical and regulatory guidelines, including GCP.

• Monitoring study progress and reporting protocol deviations device deficiencies

General support:

• Setting up and maintaining study equipment and workstations.

• Communicating with participants, study staff, sponsors, and other departments.

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As a requirement of our open positions, you must be open to the possibility of traveling for one to two weeks at a time to conduct studies in other locations outside of Colorado.

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If you are interested in any of our open positions please send your resume and cover letter to hr@parameterslab.com and specify which position you are interested in.