Clinical Research Scientist II

Springhealth; United States; À distance; USD 110 000 - 170 000; Plein temps

Résumé du poste

Spring Health is seeking a Clinical Research Scientist to join our Health Economics and Outcomes Research team. This fully remote, full-time role blends clinical research with scientific analysis and program management, roughly split 50/50.

You will design and execute rigorous studies, translate real-world clinical data into actionable insights, and coordinate clinical study activities from protocol initiation through close-out.

Qualifications

• Experience designing and executing rigorous clinical research.
• Ability to translate real-world data into actionable insights.
• Experience managing research programs, timelines, and budgets.
• Familiarity with IRB submissions and protocol compliance.
• Strong collaboration with cross-functional teams.

Responsabilités

• Publish novel, high impact academic research.
• Conduct program evaluation for network-wide tools and trainings.
• Develop and maintain detailed project plans, timelines, and budgets.
• Track study progress against milestones and identify risks.
• Coordinate cross-functional study timelines and deliverables.
• Support protocol adherence and compliance activities, including IRB submissions.

Connaissances

Clinical research

Data analysis

Program management

Cross-functional collaboration

Scientific writing

Formation

PhD or MD in a relevant field

Outils

R

SAS

Description du poste

Spring Health is looking for a Clinical Research Scientist to join our Health Economics and Outcomes Research team. This role combines clinical research and scientific analysis with research program management, with approximately 50% of time focused on each. You will design and execute rigorous research, translate real-world clinical data into actionable insights, and help coordinate clinical study activities from protocol initiation through close-out. You will work closely with scientists and cross-functional partners, with guidance and support from research leadership on study operations, prioritization, risk management, and complex program decisions. This is a full-time position that is fully remote.

What you’ll do

• Publish novel, high impact academic research
• Conduct comprehensive program evaluation for tools and trainings implemented throughout our network of psychologists and psychiatrists
• Support development and maintenance of detailed project plans, timelines, and budgets for clinical studies, with guidance from research leadership
• Track and report study progress against key milestones; identify risks or process gaps and elevate issues while supporting mitigation plans
• Coordinate cross-functional study timelines, deliverables, and dependencies to support on-time execution of clinical projects
• Support protocol adherence and compliance activities, including IRB submissions, financial tracking, and management of study protocols