Jobs at Allen Spolden

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

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

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

Provide Clinical Research support for trials, assist in protocol design, site evaluations, study monitoring, and preparation of regulatory documents.

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

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 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.

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 Staffing Manager is responsible for developing business in a metrics-driven environment, marketing to decision-makers, and building long-term relationships. They require leadership, organizational, and communication skills, and must effectively source candidates for multiple locations.

Support clinical research trials by assisting in protocol design, site evaluations, study monitoring, and report preparation under supervision.