The analyst will resolve support inquiries and technical issues for the clinical research community using IT service management tools. They will also collaborate with investigators and staff to ensure data integrity and adherence to clinical trial protocols.
Independently conduct remote and on-site clinical study monitoring visits, review site records and trial processes, document findings, and follow up on action items to support compliance with protocols, SOPs, ICH GCP, and applicable regulations. Serve as a contact for study sites, train site staff, collaborate with project teams, and support study materials, audits, document archiving, and other site management activities.
The Director of Capture Strategy & Growth will lead the end-to-end capture lifecycle and drive new business growth across federal and commercial health markets. This role involves building a qualified pipeline, architecting teaming strategies, and collaborating with executive leadership to achieve annual bookings targets.
The Senior In-House CRA assists with operational activities for clinical trial site management and monitoring to ensure compliance with protocols and regulatory requirements. They also manage essential documentation, track trial progress, and provide mentorship to junior staff members.
The Clinical Trial Manager I leads operational activities for clinical studies, overseeing monitoring teams and ensuring site performance and quality. They are responsible for tracking study timelines, managing site deliverables, and maintaining strong relationships with clients and internal collaborators.
The Principal Clinical Database Developer designs and configures electronic case report forms and clinical database study configurations within an agile team. They serve as a technical subject matter expert, providing leadership in data integration, validation, and adherence to CDISC standards.
The Study Start-Up Associate II provides administrative support for regulatory submission packages and coordinates study start-up timelines. They track essential documents, liaise with cross-functional teams, and ensure regulatory compliance throughout the site activation process.
Support and administer the company’s global privacy program, including reviewing policies and SOPs, advising business teams, maintaining privacy compliance records, and monitoring regulatory developments. Lead or support data incident investigations and negotiate privacy and security terms, including DPAs and DUAs, while collaborating with Legal, Information Security, Compliance, HR, and business stakeholders.
The Principal Statistical Programmer leads the development, validation, and maintenance of SDTM and ADaM datasets for clinical trials and regulatory submissions. They serve as a technical expert, providing oversight and mentoring to junior staff while ensuring compliance with industry standards.
The Principal Biostatistician leads the design, analysis, and interpretation of clinical trial data while ensuring compliance with regulatory standards. They collaborate with cross-functional teams and provide mentorship to junior staff to support drug development programs.
The specialist will own full-cycle recruiting for consulting roles, managing the entire process from intake to offer acceptance. They will also build proactive sourcing strategies, manage recruiting budgets, and use data to report on key hiring metrics.
The Principal Statistical Programmer leads the development, validation, and maintenance of SDTM and ADaM datasets while providing technical oversight for clinical trials. They ensure programming deliverables comply with regulatory standards and support complex submissions to authorities like the FDA and EMA.
The Marketing Specialist will execute and coordinate multi-channel marketing campaigns and product launches to support business objectives. They are responsible for tracking campaign performance, analyzing data, and providing actionable insights to commercial leadership.
The Project Manager is responsible for independently managing smaller or less complex government-funded projects, including ownership of timelines, coordination, and day-to-day execution. They also lead cross-functional teams, manage project budgets, and identify and mitigate risks to ensure project objectives are met.
The Associate Clinical Data Manager assists with data management activities, including the documentation, testing, and implementation of clinical data collection studies. They collaborate with cross-functional teams to ensure the completeness and accuracy of study data within electronic databases throughout the research lifecycle.
The Computational Biologist will design and implement AI/ML models for biomedical datasets to support precision oncology and translational research. They will also develop and optimize bioinformatics pipelines while ensuring high-quality, actionable reporting for stakeholders.
The Senior Statistical Programmer is responsible for programming, validating, and delivering CDISC-compliant datasets and analysis outputs for clinical trials. They will serve as a lead programmer, collaborating with cross-functional teams to ensure high-quality regulatory submissions.
The Clinical Research Associate II monitors clinical study sites remotely and on-site to ensure compliance with protocols, SOPs, and regulatory requirements. They are responsible for conducting site visits, verifying source data, managing site documentation, and facilitating communication between site personnel and the project team.
The Scientific Director will lead complex multi-center clinical trial programs and oversee all aspects of the Statistical and Data Coordinating Center. They are responsible for building relationships with government sponsors, providing statistical oversight, and supporting business development initiatives.
The Senior Biostatistician Manager oversees statistical activities and deliverables across a broad research area while providing guidance to senior statistical staff. They are responsible for managing budgets, personnel, and client relationships to ensure high-quality, timely project completion.
The Director of Government Operations Strategy oversees the development and implementation of operational strategies for government-funded clinical research opportunities. This role involves managing budgets, coordinating with cross-functional teams, and leading the proposal process to ensure competitive and compliant bids.
The Sr. Biostatistician Manager oversees statistical activities, deliverables, and resources across a broad research area while providing guidance to senior staff. They serve as a key client point of contact, manage project budgets, and ensure all statistical work meets quality and regulatory standards.
The Clinical Data Manager oversees the collection, processing, and management of clinical trial data to ensure accuracy and regulatory compliance. They are responsible for developing data management plans, managing EDC systems, and coordinating with cross-functional teams to ensure timely database locks.
The Associate Director provides leadership and subject matter expertise for the statistical design, analysis, and interpretation of clinical trial data. They oversee the development of statistical analysis plans and collaborate with cross-functional teams to ensure the scientific rigor of clinical development programs.
The Senior Director of Quality Assurance directs the global clinical quality strategy and oversees the Quality Management System to ensure regulatory compliance. They lead a global team of professionals, manage internal and customer audit programs, and champion inspection readiness initiatives.
The Clinical Project Coordinator supports project teams by managing logistics, including scheduling meetings, tracking deadlines, and compiling project deliverables. They also assist in maintaining project systems, documentation, and communication between project staff and sponsors.
The Manager of Regulatory Affairs leads regulatory strategy for clinical programs, advising internal teams and clients while facilitating dialogue with the FDA. They also provide direct supervision to a team of regulatory professionals, overseeing operational deliverables and ensuring compliance with global regulatory standards.
The Clinical Data Manager oversees the collection, processing, and management of clinical trial data to ensure accuracy and compliance with regulatory standards. They are responsible for developing data management plans, maintaining EDC systems, and coordinating with cross-functional teams to ensure timely database locks.
The Global Project Manager serves as the primary lead for biopharmaceutical clinical trials, managing project delivery, budgets, and timelines. They act as the main point of contact for clients, driving team efficiency and ensuring high-quality project outcomes.
The Associate Biostatistician collaborates with study teams to determine study designs, review protocols, and develop statistical analysis plans. They also generate reports for data monitoring, regulatory bodies, and scientific publications while ensuring compliance with industry standards.
The Director of Business Development is responsible for driving revenue growth by identifying, developing, and closing new business opportunities across clinical research services and technology solutions. This role involves strategic account management, leading pursuit teams, and positioning the company as a trusted partner to pharmaceutical and biotechnology organizations.
The Principal Clinical Data Manager provides leadership and subject matter expertise throughout the clinical research study lifecycle, from design to final analysis. They are responsible for ensuring data accuracy, managing EDC systems, and mentoring data management staff.
The Project Control Analyst manages financial models, revenue forecasts, and project-level reporting for government contracts. They collaborate with internal teams to monitor budgets, track project transactions, and ensure compliance with financial policies.
The Director of Business Development is responsible for driving revenue growth by identifying, developing, and closing new business opportunities across clinical research services and technology solutions. This role involves strategic account management, cross-functional leadership, and positioning the company as a trusted partner to pharmaceutical and biotechnology organizations.
The biostatistician will collaborate with clinical investigators to design studies, develop protocols, and write statistical analysis plans. They are also responsible for performing statistical analyses, ensuring data safety, and reporting findings for regulatory bodies and peer-reviewed publications.
The Associate Project Leader serves as the matrix leader for government-sponsored clinical research projects, ensuring successful delivery within budget and timeline constraints. They are responsible for managing project teams, mitigating risks, and maintaining strong relationships with clients and stakeholders.
Manage proposal response teams to develop high-quality, compliant, and timely proposals for government and biomedical research solicitations. Collaborate with capture teams to implement win strategies while maintaining proposal content libraries and project timelines.
The Associate Director of Biostatistics provides leadership and subject matter expertise for the statistical design, analysis, and interpretation of clinical trial data. They oversee the development of statistical analysis plans and collaborate with cross-functional teams to ensure scientific rigor and regulatory compliance.
The Clinical Research Associate II is responsible for monitoring clinical study sites to ensure trials are conducted in accordance with protocols, SOPs, and regulatory requirements. They perform remote and on-site monitoring visits, manage site documentation, and facilitate communication between site personnel and the project team.
The Senior Statistical Programmer is responsible for programming, validating, and delivering CDISC-compliant datasets and statistical outputs for clinical trials. They will collaborate with cross-functional teams to support regulatory submissions and ensure high-quality programming deliverables.
The Biostatistician Manager oversees statistical activities across clinical research studies and leads a team of statisticians and SAS programmers. They collaborate with investigators on study design, perform statistical analyses, and ensure high-quality deliverables for regulatory bodies.
The Sr. Biostatistician Manager oversees statistical activities, deliverables, and resources across a broad research area while providing guidance to senior staff. They serve as a key client point of contact, manage budgets, and participate in strategic planning and recruitment for the department.
