Top Remote Biotech Jobs in Rochester, NY

The Senior Clinical Trials Scientist is responsible for leading the scientific execution of Phase II-III clinical trials, contributing to study design, regulatory documentation, and mentoring junior staff.

The Sales Operations Analyst manages CRM hygiene, supports deal processes, conducts reporting and analytics, and implements AI solutions to enhance sales workflows.

Develop and maintain scalable backend services and APIs for scientific research, ensuring performance, security, and high availability. Collaborate on product direction and troubleshoot issues while advocating for software best practices.

The Senior Clinical Programmer will develop and maintain programming for clinical trial data, ensuring data quality and compliance, while collaborating with other stakeholders. Responsibilities include troubleshooting, documentation, and mentoring junior programmers.

The Clinical Data Manager II will oversee data management for clinical studies, ensuring data accuracy, consistency, and compliance with protocols. Tasks include data review, discrepancy resolution, and collaboration with cross-functional teams.

The Sr. Manager/Associate Director, Market Access will shape and execute the commercial payer strategy, engage stakeholders, and improve patient access to diagnostics through strategic collaboration and advocacy efforts.

The Compliance Manager, Transparency ensures compliance with reporting regulations, manages data accuracy, supports audits, and collaborates across teams for effective compliance processes.

As a Senior Data Scientist, you will develop statistical models and machine learning algorithms to improve patient enrollment and trial management while ensuring compliance in a healthcare data environment.

As a Senior Machine Learning Engineer, you will develop and deploy AI-driven products to enhance clinical trials, collaborating with teams to improve patient care through scalable machine learning solutions.

The role leads the US Study and Site Operations Contracts and Payment team, ensuring quality oversight in contract negotiations, compliance, and timely research study start-ups while managing a team of Contract and Finance managers.

As a Global Study Manager at ICON, you will lead project management activities, develop plans, manage cross-functional teams, and ensure successful project execution.

The Global Study Manager will lead project management activities, develop plans, guide teams, and collaborate with stakeholders to achieve project goals in oncology clinical research.

The Global Study Manager oversees project management activities in oncology, ensuring successful project execution by leading teams, developing project plans, and maintaining stakeholder communication.

The role involves managing recruitment and retention strategies for clinical trials, collaborating with teams, and overseeing vendor management to ensure patient-focused solutions and compliance.