Top Pharmaceutical Jobs in Orlando, FL

The Outside Sales Executive is responsible for marketing and selling digital health programs to physician offices and health systems, while traveling within a specified territory.

The Specialty Care Field Medical Director drives medical strategies, engages with external medical stakeholders, and delivers educational content to enhance patient care initiatives. Responsibilities include fostering collaborations, managing projects across teams, and providing scientific insights for clinical development.

The Sr. Software Engineer designs, implements, and maintains scalable cloud services, contributes to team processes, and acts as a subject matter expert while leading projects and mentoring others.

The Senior Clinical Data Manager oversees clinical trial databases, ensures data quality, and acts as a liaison between eClinical and sponsor personnel, managing data management tasks across projects.

The Sales Director will lead the sales process to close partnerships with research sites, managing all sales activities including discovery and negotiation, while collaborating with Customer Success for onboarding.

The role involves creating performance-driven paid social content, owning creative processes, analyzing data for design improvement, and collaborating with a copywriter to deliver effective ads across platforms.

The Oncology Account Manager will build relationships with healthcare professionals, sell LOQTORZI, and manage business plans and sales strategies for oncology products.

The Clinical Scientist collaborates with Medical Directors to develop medical plans, reviews data for trends, manages project scopes, and ensures adherence to clinical protocols while participating in audits and meetings to improve study integrity.

The Clinical Scientist supports medical plan development, data analysis, and medical reviews while ensuring compliance with guidelines and project milestones.

The Clinical Scientist in Oncology collaborates with Medical Directors to develop medical plans, perform data reviews, author queries, and manage project scope and quality, ensuring adherence to guidelines and timely project delivery.

The Senior Biostatistician I will lead early phase clinical trials, provide statistical inputs for protocols and reports, and mentor junior statisticians.

The Lead CRA manages clinical trial sites, ensures compliance with regulations, mentors CRAs, and oversees data integrity. Responsibilities include site management, issue resolution, and collaboration with cross-functional teams.

As a Senior Clinical Research Associate, you will manage clinical trials, ensuring compliance and data integrity, while collaborating with site staff and preparing study documentation.

The Scientific Writer will draft and manage nonclinical pharmacology and toxicology documents, supporting scientists and regulatory affairs while ensuring submission deadlines are met.