Top Entry Level Biotech Jobs

The Associate Scientist in Vaccines will conduct immunological assays, support vaccine clinical development, analyze data, and collaborate in a team environment to deliver effective treatments.

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Seeking a Systems Administrator to join Schrodinger, focusing on maintaining IT infrastructure, ensuring systems performance, and supporting user needs. Applicants should embody team's values of engagement and collaboration.

The role involves managing customer inquiries, coordinating with labs, maintaining relationships, and ensuring high customer satisfaction in a healthcare setting.

The Enrollment Research Assistant supports participant evaluation and enrollment in clinical trials, ensuring compliance with protocols and assisting with administrative tasks like scheduling and documentation.

The Clinical Research Assistant supports clinical trial operations, participant interactions, data management, and regulatory compliance under supervision, helping ensure studies run smoothly.

The Enrollment RA assists in evaluating, triaging, and enrolling participants for clinical trials, supporting study operations and ensuring compliance with protocols.

The Site Contracts Lead will collaborate globally with customers in drug development, ensure compliance, and facilitate contract negotiations.

The Clinical Data Reviewer will work in the oncology field, ensuring data integrity for clinical trials and collaborating with teams to meet customer needs.

As a Site Management Associate I, you will assist in monitoring clinical trial sites, ensuring compliance with protocols, and supporting site management activities.

Conduct site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; perform data review and query resolution; contribute to study documentation and clinical study reports.

Support clinical teams inhouse by managing study documentation, overseeing Trial Master Files, ensuring compliance, and assisting with study logistics and communications.

The GMP Biomanufacturing Operator I will execute manufacturing processes in a GMP setting, follow safety and quality standards, and collaborate to improve processes.

The GMP Biomanufacturing Operator I executes production events in a GMP environment, adhering to safety protocols and manufacturing processes, working in a team setting to improve procedures.