Jobs at Allen Spolden

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

The role involves performing administrative duties, maintaining project data, preparing payroll forms, and coordinating department activities and schedules. Oversight of support staff is also included.

The Senior Quality Microbiologist conducts microbiological assays for pharmaceutical quality control, prepares samples, documents results, calibrates instruments, and ensures compliance with CGMP regulations.

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

The Quality Assurance Engineer II will focus on the manufacturing of sterile disposable products, utilizing statistical techniques and ensuring quality through collaboration and effective communication.

The Quality Assurance Engineer II is responsible for ensuring the manufacture of sterile disposable products, utilizing statistical techniques and collaboration in cross-functional teams.

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

The Cath Lab/IRB Technologist assists physicians in interventional procedures, prepares equipment, applies safety standards, and collaborates with the care team while ensuring patient-centered care.

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

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

Provide clinical research support for trials by assisting in protocol design, site evaluation, budget procurement, monitoring studies, and preparing reports.

The Clinical Director is responsible for identifying hospital underpayments, submitting appeals for additional reimbursement, and ensuring quality standards. They also coach team members, participate in meetings, and manage client relationships while adhering to HIPAA.

The Clinical Research Associate 1 supports clinical trials by preparing protocols, monitoring sites, managing documentation, and reporting on study progress under supervision.

This role involves supporting clinical trials through protocol preparation, monitoring site compliance, managing budgets and regulatory documents, and conducting site visits.

The Clinical Trial Manager oversees all clinical aspects of studies, manages budgets, trains staff, engages with stakeholders, and mitigates risks.

Responsible for routine administrative duties, maintaining project data, preparing payroll forms, answering questions, and overseeing support staff work.

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

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

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.

The Quality Manager will assess patients' needs for behavioral care, manage treatment plans, coordinate benefits, and work with diverse community populations to enhance treatment effectiveness.