Jobs at Allen Spolden

The Senior Scientist coordinates R&D assignments, applies scientific methods, conducts evaluations, prepares reports, and ensures compliance with quality systems, focusing on product development.

The Compliance Coordinator ensures compliance with standards, manages quality improvement strategies, prepares reports, and supports data-driven initiatives for childcare and health services.

Assist in the design and monitoring of clinical trials, prepare protocols and necessary materials, conduct site visits, and ensure compliance with regulations.

Assist in clinical research trials by supporting study teams, preparing documents, conducting site visits, and ensuring adherence to protocols.

The Clinical Research Associate 1 assists in clinical trial operations, including protocol design, site evaluations, study monitoring, and documentation for regulatory submissions.

The Analytical Scientist II develops and optimizes analytical methods, troubleshoots issues, conducts experiments, and prepares detailed documentation in a GXP-compliant environment.

Support clinical research activities, design protocols, generate SOPs, monitor studies, and prepare reports under supervision. Requires attention to detail and communication skills.

The Scientist in Analytical Development develops and implements analytical methods for small molecules and oligonucleotides, coordinates projects, performs lab assignments, and troubleshoots analytical issues.

Assist in the design and preparation of clinical protocols, conduct site evaluations, manage projects, monitor studies, and maintain documentation.

Support laboratory experiments by preparing samples and reagents, performing routine tests, collecting and recording data, maintaining lab records and equipment, ensuring safety and organization, and assisting scientists with reports and research projects.

Support coordination and administration of clinical studies remotely: maintain regulatory files, prepare and enter study documentation, coordinate participant scheduling, ensure data quality and GCP compliance, and assist research teams.

Support planning and execution of clinical trials by coordinating site communication, maintaining TMF and regulatory documents, tracking milestones, assisting data management and study start-up, and ensuring ICH-GCP and SOP compliance.