Science Jobs in Blue Bell, South Dakota — April 2026

Overview

Support the design, implementation, and management of clinical trials by coordinating site initiation, patient recruitment, and data collection. Maintain comprehensive study documentation and collaborate with cross-functional teams to ensure adherence to protocols and regulatory guidelines.

Overview

Serve as the primary contact between investigational sites and sponsors while conducting various site visits including selection, initiation, and close-out. Ensure site compliance with ICH-GCP and regulations while managing data quality and patient safety reporting.

Overview

Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and driving high-quality data entry.

Overview

Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with regulations. Oversee patient safety, drug accountability, and data quality while collaborating with cross-functional clinical teams.

Overview

Provide care, supervision, and habilitation to individuals with intellectual and developmental disabilities across various residential settings. Act as a caregiver and life coach to promote independence through assistance with daily living activities and community integration.

Overview

Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data entry and site documentation.

Overview

Serve as the primary contact between investigational sites and sponsors while conducting various site visits including initiation and close-out. Ensure site compliance with ICH-GCP and regulations while managing data queries and patient safety reporting.

Overview

Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data quality and site documentation.

Overview

The Sr. CRA is responsible for managing investigative sites and performing monitoring activities throughout the clinical trial lifecycle to ensure data integrity and subject safety. Key duties include conducting site visits, managing essential documents, and ensuring compliance with protocols and regulatory standards.

Overview

The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.

Overview

Support the design, implementation, and management of clinical trials by coordinating site initiation and patient recruitment. Maintain comprehensive study documentation and collaborate with cross-functional teams to ensure regulatory compliance and data accuracy.

Overview

The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.