Director of Scientific Affairs
Jobgether, Turkey, NC, United States
Director of Scientific Affairs (Turkey)
We are looking for a visionary scientific leader to drive the strategy and execution of clinical evidence generation in a cutting‑edge digital health environment. This role will lead large‑scale clinical studies, manage grant applications, and foster academic collaborations to translate extensive patient data into impactful publications. You will leverage advanced analytics and AI‑powered tools to optimize research operations, while also contributing to business strategy by identifying high‑value funding opportunities and strategic partnerships. The ideal candidate thrives in a dynamic, fast‑paced setting, balancing rigorous scientific oversight with innovative technology‑driven approaches to improve patient outcomes and advance the field of medical extended reality.
Accountabilities
Lead the end‑to‑end process of identifying, writing, and submitting federal, state, and foundation grant applications to secure non‑dilutive funding.
Develop and maintain a strategic grant pipeline aligned with clinical priorities and organizational objectives.
Design and oversee randomized controlled trials (RCTs) and other clinical studies, ensuring regulatory and ethical compliance across multiple sites.
Manage collaborations with academic institutions, clinical partners, and CROs to execute research programs on time and within budget.
Conduct statistical analyses of large‑scale clinical datasets, translating insights into actionable recommendations and peer‑reviewed publications.
Deploy AI tools and automated workflows to accelerate literature reviews, data processing, and report generation.
Represent the organization in academic and clinical communities, building thought leadership and credibility in the field of medical XR.
Requirements
Ph.D. or equivalent advanced degree in Clinical Psychology, Neuroscience, Public Health, Biostatistics, or a related field.
Proven success in writing and securing significant research grants (e.g., NIH, NSF, DOD, or major foundations).
Extensive experience designing and managing complex clinical research projects, particularly RCTs.
Strong track record of first‑author or co‑authored peer‑reviewed publications.
Proficiency in statistical programming (Python or R) and experience with SQL and cloud‑based data warehouses for large‑scale data analysis.
Ability to bridge rigorous academic research with fast‑paced health‑tech operations.
Experience leveraging AI tools and agent platforms to enhance research efficiency is highly desirable.
Benefits
Competitive base salary commensurate with experience, with performance‑based bonuses tied to research and grant milestones.
Equity participation in a high‑growth health‑tech company.
Comprehensive health, dental, and vision insurance.
401(k) retirement plan.
15 days of PTO in the first year, with growth opportunities as the company scales.
Fully remote work flexibility and collaboration with a global team of clinicians, engineers, and researchers.
Opportunities to publish novel research findings and contribute to thought leadership in an emerging field.
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Accountabilities
Lead the end‑to‑end process of identifying, writing, and submitting federal, state, and foundation grant applications to secure non‑dilutive funding.
Develop and maintain a strategic grant pipeline aligned with clinical priorities and organizational objectives.
Design and oversee randomized controlled trials (RCTs) and other clinical studies, ensuring regulatory and ethical compliance across multiple sites.
Manage collaborations with academic institutions, clinical partners, and CROs to execute research programs on time and within budget.
Conduct statistical analyses of large‑scale clinical datasets, translating insights into actionable recommendations and peer‑reviewed publications.
Deploy AI tools and automated workflows to accelerate literature reviews, data processing, and report generation.
Represent the organization in academic and clinical communities, building thought leadership and credibility in the field of medical XR.
Requirements
Ph.D. or equivalent advanced degree in Clinical Psychology, Neuroscience, Public Health, Biostatistics, or a related field.
Proven success in writing and securing significant research grants (e.g., NIH, NSF, DOD, or major foundations).
Extensive experience designing and managing complex clinical research projects, particularly RCTs.
Strong track record of first‑author or co‑authored peer‑reviewed publications.
Proficiency in statistical programming (Python or R) and experience with SQL and cloud‑based data warehouses for large‑scale data analysis.
Ability to bridge rigorous academic research with fast‑paced health‑tech operations.
Experience leveraging AI tools and agent platforms to enhance research efficiency is highly desirable.
Benefits
Competitive base salary commensurate with experience, with performance‑based bonuses tied to research and grant milestones.
Equity participation in a high‑growth health‑tech company.
Comprehensive health, dental, and vision insurance.
401(k) retirement plan.
15 days of PTO in the first year, with growth opportunities as the company scales.
Fully remote work flexibility and collaboration with a global team of clinicians, engineers, and researchers.
Opportunities to publish novel research findings and contribute to thought leadership in an emerging field.
#J-18808-Ljbffr