Imaging Clinical Research Scientist

This is a fully remote position, open to applicants in United States.

📋 Description

• Oversee the design and implementation of integrated clinical development programs for diagnostic radiopharmaceuticals throughout early- and late-phase development.

• Establish clinical strategies, endpoints, patient demographics, and imaging standards.

• Create studies that assess diagnostic accuracy, imaging timing, patient-selection biomarkers, and comparative effectiveness against standard imaging practices.

• Act as a scientific authority in PET, SPECT, CT, and MRI molecular imaging techniques.

• Analyze and interpret molecular imaging data, including tumor localization, tracer biodistribution, dosimetry, and longitudinal response evaluations.

• Assess imaging biomarkers for patient stratification, disease activity evaluation, and disease monitoring.

• Review imaging performance metrics such as sensitivity, specificity, standardized uptake values, and tumor-to-background ratios.

• Offer strategic insights on advanced image-analysis techniques and quantitative assessments.

• Utilize disease biology knowledge to inform diagnostic imaging program strategies.

• Collaborate with physicians, scientists, medical physicists, imaging operations, and advanced image-analysis teams.

• Lead cross-functional initiatives and coordinate with CROs, academic institutions, software developers, and scanner manufacturers.

• Assess new imaging technologies, modeling techniques, and artificial intelligence applications for clinical programs.

• Author and review Investigator’s Brochures, protocols, amendments, clinical study reports, and regulatory briefing documents.

• Contribute to technical manuals and documentation related to imaging trials.

• Disseminate scientific findings through presentations, conference abstracts, and publications in peer-reviewed journals.

• Execute other duties as assigned.

⛳️ Requirements

• PhD in a relevant discipline.

• At least 5 years of experience in clinical development.

• Minimum of 3 years of experience in the industry.

• Experience in tracer development is strongly preferred.

• Background in oncology, immunology, and/or cardiology is highly desirable.

• Excellent problem-solving abilities.

• Knowledge of Good Clinical Practice (GCP) and regulatory standards.

• Capability to balance scientific and business objectives.

• Proven communication, collaboration, organizational, and influencing capabilities.

• Proficiency in both written and spoken English.

• Willingness to travel approximately 10–15% of the time.

🏝️ Benefits

• Company bonus based on both company and individual performance.

• Company-sponsored 401(k) plan.

• Pension plan.

• Vacation benefits.

• Medical, dental, vision, and prescription drug coverage.

• Flexible spending accounts for healthcare and/or dependent day care.

• Life insurance and death benefits.

• Various time off and leave of absence benefits.

• Well-being benefits, including an employee assistance program, fitness benefits, and employee clubs and activities.

• Employee resource groups available to all staff.