Top Remote Biotech Jobs

The Account Manager drives sales and growth of POC product lines in Eastern South Florida, focusing on customer retention and satisfaction while achieving sales targets.

Develop and maintain backend solutions, ensuring performance, security, and regulatory compliance, while collaborating in cross-functional teams.

As an Android Engineer, you will design and maintain code for Android apps, collaborate with cross-functional teams, and improve the Android codebase while ensuring quality through testing.

As an iOS Engineer, you will develop and maintain features for the Oura app, collaborating with various teams to enhance user experience and code quality.

The Senior Account Manager drives sales growth by expanding CST's presence within key accounts, focusing on relationships and tailored strategies for revenue growth.

The Director in the Modeling CoE will lead the HEOR Modeling team in developing health economic models for HTA submissions, provide strategic support, and ensure quality assurance of models developed both in-house and by vendors.

The Product Manager defines and improves healthcare technology products, collaborating with stakeholders and ensuring compliance with regulations within an Agile framework.

Responsible for monitoring cardiovascular medical device studies, ensuring compliance with FDA regulations, and fostering effective relationships with stakeholders.

As a Clinical Research Associate, you will manage site visits, ensure compliance with regulations, and oversee patient safety and data quality in oncology trials.

Oversee cardiovascular clinical trials, ensuring compliance with regulations while managing site relationships and communication. Requires 3 years of monitoring experience and strong problem-solving skills.

The role involves budgeting for clinical trials, negotiating contracts, collaborating with sponsors, ensuring compliance, and training junior staff.

The CRA I conducts site management duties such as monitoring and ensuring compliance with regulatory standards. They lead site interactions, support patient recruitment, document site activities, and manage communication with project teams.

Manage negotiation and execution of clinical study agreements (CTAs) while ensuring compliance with sponsor and company requirements. Build strong relationships with stakeholders and support operational initiatives for site contracting and budgeting goals.

The Associate Scientific Director will lead pharmacometrics analyses, contribute to drug development strategies, mentor colleagues, and support decision-making through advanced quantitative modeling.

The Senior Principal Analyst, Statistical Programming leads statistical programming activities, manages resources, and oversees the creation of analysis datasets and electronic submissions while ensuring compliance with standards.

The Director of Principal Management leads business strategies in the CASE market, oversees sales growth, manages strategic relationships, and coordinates technical projects with various teams to achieve organizational goals.

The Senior Clinical Research Associate oversees Phase I-IV clinical trials, ensuring compliance and data integrity while managing site relationships and monitoring activities, with extensive travel required.

Lead US market access strategy for launch and inline brands, develop 3–5 year access plans, coordinate cross-functional execution (pricing, contracting, marketing, legal), manage budgets, vendor RFPs, and ensure payer coverage, affordability, and durable product value.