Job description
VitaNova Medical Institute is a premier center for specialized medicine, leveraging genomics, pharmacology, and data science to deliver precision therapies. We are seeking a Senior Specialist in Personalized Medicine to lead clinical programs, advance biomarker-driven treatments, and collaborate across disciplines.
In this role you will partner with clinicians, researchers, and biostatisticians to design and execute personalized medicine strategies, manage clinical study activities, and ensure rigorous regulatory compliance. You will influence patient outcomes, mentor teammates, and contribute to thought leadership through publications and conferences.
What you will gain is an opportunity to shape the direction of cutting-edge therapies in a collaborative, data-driven environment, with access to world-class facilities and ongoing professional development.
Responsibility
- Lead the design and execution of personalized medicine programs, including biomarker development and companion diagnostic strategies.
- Manage and monitor clinical studies from planning through close-out, ensuring regulatory compliance and high data quality.
- Collaborate with clinicians, scientists, and biostatisticians to translate genomic and proteomic data into actionable patient care plans.
- Mentor junior staff, coordinate cross-functional teams, and drive a culture of scientific excellence.
- Prepare and contribute to scientific manuscripts, conference presentations, and regulatory submissions as needed.
- Develop and implement protocols for real world evidence generation and postmarketing surveillance where applicable.
- Represent the institute in external partnerships, advisory boards, and industry forums.
Qualification
- Advanced degree (MD or PhD) in medicine, genomics, bioinformatics, or a closely related field; board certification preferred.
- Minimum 5 years of experience in personalized or precision medicine, clinical research, or translational science.
- Proven track record in designing and executing biomarker-driven studies and data-driven decision making.
- Strong knowledge of regulatory standards (FDA/EMA), good clinical practice GCP, and ethical considerations.
- Proficiency with biostatistics, data analysis tools, and data visualization; experience with IRB submissions and regulatory documentation.
- Excellent communication and collaboration skills; ability to influence cross-functional stakeholders.
- Demonstrated ability to publish in peer-reviewed journals and present at conferences.
- Commitment to diversity, equity, and patient-centered care.