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

Position Summary:

The Clinical Data Coordinator supports the Clinical Data Manager in delivery of Data Management contracted services on assigned projects. This includes responsibility for tasks and processes associated with database build, data review and closure of the database.

Location: Remote

Position Summary:

The Clinical Trial Assistant (CTA) plays a vital role in supporting the successful execution of clinical trials by ensuring high-quality administrative, regulatory, and operational support to project teams. This position involves maintaining Trial Master Files (TMF), coordinating site communications, assisting with regulatory document collection, tracking study progress, and supporting data review activities. The CTA serves as a key point of contact between clinical monitoring staff and investigative sites, contributing to smooth study conduct and compliance with regulatory requirements.

Location: St. Petersburg, FL

Position Summary:

We are seeking a detail-oriented and analytical Contract Analyst to join our team. The ideal candidate will play a crucial role in managing contracts, ensuring compliance with regulations, and supporting business development initiatives. This position work internally with Project Managers/Directors, Financial Department as well as externally with Sponsor, Investigator sites, and vendor account representatives.

Location: Remote

Position Summary:

The Senior Statistical Programmer provides advanced technical expertise to plan, coordinate, and execute programming deliverables across all phases of clinical studies. This role is responsible for developing high-quality datasets and producing Tables, Listings, and Figures (TLFs) in accordance with project specifications and regulatory standards. The Senior Statistical Programmer leads the implementation of integrated programming solutions and ensures rigorous quality control throughout the project lifecycle. In addition to hands-on programming, this position contributes to departmental leadership by providing guidance, mentorship, and technical oversight. The role involves close collaboration with cross-functional teams including clinical operations, data management, biostatistics, and external clients or partners to support timely and accurate delivery of analysis results.

Location: Remote

Position Summary:

The Clinical Project Financial Analyst plays a key role in managing the financial accuracy and integrity of clinical trial projects. This position supports invoicing, reconciliation, and tracking of unbilled amounts by collaborating closely with internal teams and external partners. Responsibilities include verifying site invoicing against contract terms, resolving discrepancies with site staff, supporting monthly sponsor billing, and ensuring accurate payments to vendors. The analyst also assists with account reconciliation, project closeouts, and ad hoc financial analysis.

Location: St. Petersburg, FL

Position Summary:

The Recruiter is responsible for the entire recruiting life cycle, from job requisition to hire. The Recruiter should possess extensive knowledge of recruitment, with experience in life sciences, clinical trials, or related industries. Will be skilled at identifying, assessing, and engaging high quality talent throughout the organization. Will possess solid understand functional areas of the CRO business (especially clinical ops) to support and develop thoughtful and engaging relationships with hiring managers, department heads and leaders.

Location: Remote