Clinical Program Lead - Diagnostics (Multi-Site)

SiPhox Health; Burlington (MA); On-site; USD 140,000 - 190,000; Full time

Job summary

SiPhox Health is seeking a Clinical Program Manager to own the operational execution of clinical studies for our diagnostic products. You will collaborate with Quality, Regulatory, Assay Development, Engineering, Software, and external sites to translate study protocols into well-run programs and submission-ready data.

In this hands-on role, you will manage site startup through study closeout, coordinate sample handling, device logistics, and data reconciliation, and ensure compliance with

Qualifications

• Bachelor's degree in life sciences or similar field.
• 5+ years managing clinical studies in regulated settings.
• Experience coordinating multi-site clinical studies.
• Strong understanding of study operations, documentation, and data integrity.
• Experience working with investigators, coordinators, labs, and vendors.
• Excellent project management and organizational skills.

Responsibilities

• Manage clinical studies from protocol finalization through closeout.
• Translate protocols into operational plans, timelines, and site procedures.
• Coordinate startup activities across internal teams and external sites.
• Maintain the master study schedule and monitor enrollment and data quality.
• Ensure activities comply with protocols, SOPs, and regulatory requirements.
• Coordinate site initiation, training, and ongoing monitoring.

Skills

Project management

Organizational skills

Communication skills

Stakeholder management

Multi-site coordination

Data integrity

Education

Bachelor's degree in life sciences, biomedical engineering, clinical research, nursing, or related field

Job description

SiPhox Health is seeking a Clinical Program Manager to own the operational execution of clinical studies for our diagnostic products. You will collaborate with Quality, Regulatory, Assay Development, Engineering, Software, and external sites to translate study protocols into well-run programs and submission-ready data.

In this hands-on role, you will manage site startup through study closeout, coordinate sample handling, device logistics, and data reconciliation, and ensure compliance with