Jobs at Allen Spolden

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.

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 Senior Recruiting Manager leads the recruiting team, develops growth plans, and enhances strategies to attract top talent, while ensuring inclusive team culture.

The Recruiting Manager motivates the team, conducts one-on-one development meetings, consults on recruiting strategies, acts as a brand ambassador, and tracks program successes through metrics.

The Safety Associate supports clinical trial safety management by ensuring compliance with regulations, managing adverse event reports, and preparing safety data and reports for stakeholders.

Support clinical trials by assisting in protocol design, site evaluations, monitoring studies, and preparing reports and regulatory submissions.

Provide clinical research support for trials, assist in protocol design, monitor studies, prepare reports, and maintain files.

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.

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 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 Data Manager oversees data management activities, ensuring efficient conduct of projects, regulatory compliance, and quality data validation throughout the study lifecycle.

The Senior Data Scientist will manage data collection, design study protocols, train juniors, lead report development, and support innovative analytics tools.

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

The Senior Data Scientist oversees data collection and preparation, designs study protocols, leads report development, trains junior employees, and manages project workstreams while collaborating with team members to optimize business performance.

Act as primary contact for sites, adapt consent forms, assist in contract negotiations, update documents for studies, and support IRB submissions.