Jobs at Allen Spolden

Responsible for generating diagnostic images, assisting in procedures, ensuring patient safety, and maintaining ultrasound equipment in a healthcare setting.

The Account Executive is responsible for business development by building client relationships and fulfilling staffing solutions with strong customer service. Achieve business development goals through contacting clients and matching candidates with job orders.

The Compliance Coordinator ensures compliance with performance standards and regulations, implements quality improvement strategies, manages documentation, and supports staff training and data collection.

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 manages lab operations, ensuring compliance with GXP standards.

The Clinical Research Associate 1 supports clinical trials by assisting with protocol preparation, site evaluation, monitoring studies, and maintaining documentation.

The Clinical Research Associate 1 supports clinical trials by designing protocols, monitoring site adherence, and managing documentation.

Provide support for clinical trials, assist in protocol design, conduct monitoring, evaluate clinical sites, and maintain study documentation.

The role involves ensuring quality in adverse event report processing, collaborating with teams, conducting training, and maintaining regulatory compliance in pharmacovigilance.

Assists the clinical study team in research trials, including protocol design, site evaluations, study monitoring, and report preparation.

The Sr. Clinical Research Associate will support clinical studies by preparing protocols, monitoring sites, maintaining documents, and ensuring regulatory compliance.

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

The role requires ensuring the quality of sterile disposable products, applying statistical techniques, and collaborating in a medical device environment with a focus on reporting and teamwork.

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

The Director of Quality develops and maintains a cGMP Quality System, oversees Quality departments, audits compliance, and manages staff in a pharmaceutical manufacturing setting.

Assist in clinical trial support including protocol preparation, site evaluations, monitoring studies, and reporting for regulatory submissions.

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

The role involves managing document collection for studies, adapting patient materials to specific requirements, and supporting contract negotiations. Responsibilities include updating study documents, filing quality documents, and assisting in IRB submissions under supervision.

The Clinical Research Associate II assists in clinical trials by participating in protocol design, site evaluation, monitoring, and preparing reports. Responsibilities include generating SOPs, managing documents, and ensuring regulatory compliance.

The Data Scientist II will oversee data management, design study protocols, train staff, lead report development, and manage client activities using project frameworks.