Position Summary:

The Assessments Manager, Training and Quality is responsible for developing, implementing, and overseeing training programs, quality assurance processes, subject eligibility review, and department initiatives for clinical assessments conducted within the organization. This role ensures that raters, site personnel, and internal teams maintain consistent, accurate, and high-quality administration of assessments in alignment with study protocols, regulatory requirements, and industry best practices.

Location: Remote

Position Summary:

The Clinical Programmer (CP) is responsible for the design, development, testing, implementation, maintenance, and support of programming applications external of the clinical database. The CP supports the clinical teams, sponsors, statisticians, safety\regulatory, analytical programmers, and clinical data management personnel.

Location: Remote

Position Summary:

The Senior Proposal Manager will lead, manage and execute the full life cycle of proposal development activities for Clinical Trials Proposals, and support budget generation. Manage and develop the contract development process to support an efficient, high quality, and timely RFP and contracting process. This process may include pricing, developing proposals, work orders, change orders, start-up agreements, and other contracts that support the delivery of sponsor studies.

Location: Remote

Position Summary:

The Quality Assurance (QA) Manager plays a critical role in overseeing and executing Clinical Quality Assurance activities that uphold and enhance the organization’s Quality Management System (QMS). Reporting to Quality Assurance Leadership, this position ensures compliance with ICH GCP, applicable global regulations, and internal quality standards, while fostering a culture of continuous improvement.

The QA Manager leads key quality functions, including audits, quality event management, vendor qualification, training, and risk-based quality planning. This role partners cross-functionally with clinical operations, vendors, sponsors, and leadership to maintain operational excellence and ensure that clinical research activities meet both regulatory and sponsor expectations

Location: Remote

Position Summary:

Clinical Research Associate ( Sr. CRA) is responsible for overseeing the execution of clinical trials at Investigative Sites. The Clinical Research Associate acts as a liaison between the study Sponsor, CRC and Investigative Sites. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The CRA facilitates successful execution of studies by Investigative Sites and helps to ensure the rights, safety and welfare of human research participants as well as data integrity in clinical trials.

Location: Remote