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 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 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 Senior Informaticist will lead complex technical projects, manage biomedical ontologies, and ensure semantic consistency across clinical research data. They will also mentor junior staff and provide expert guidance on data architectures and standards to internal teams and clients.
The role involves supporting enterprise informatics software systems for cancer clinical trials by managing support tickets and providing technical assistance to research sites. Additionally, the analyst will coordinate project activities, ensure compliance with regulatory standards, and prepare informatics reports for stakeholders.
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 Senior Statistical Programmer will contribute to clinical research projects by applying statistical programming expertise. They will support the development of medical discoveries across various therapeutic areas including vaccines and rare diseases.
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 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, managing EDC systems, and coordinating with cross-functional teams to ensure timely database locks.
The Associate Director/Director will lead global statistical programming strategy and oversee the delivery of high-quality, regulatory-compliant datasets and reports for clinical trials. This role involves managing programming teams, driving process innovation, and collaborating with cross-functional stakeholders to ensure successful regulatory submissions.
The Statistical Programming Manager provides oversight for complex clinical research projects and ensures the timely delivery of regulatory submission deliverables. They are responsible for managing staff, mentoring team members, and improving programming documentation and standardization processes.
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 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 manager oversees clinical trial operations, project resourcing, and staff development to ensure high-quality delivery and compliance. They also manage financial budgets, drive process improvements, and act as a key escalation point for project-related risks.
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 Clinical Research Associate II is responsible for monitoring clinical study sites both remotely and on-site to ensure compliance with protocols, SOPs, and regulatory requirements. They conduct site visits, perform source data verification, and serve as the primary point of contact for site personnel to resolve study-related issues.
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 Senior In-House CRA assists with operational activities for site management and monitoring of clinical trials to ensure compliance with protocols and regulatory requirements. They also track trial progress, manage essential documents, and provide mentorship to junior staff.
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 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.
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 Clinical Research Associate II monitors clinical study sites to ensure trials are conducted in accordance with protocols, SOPs, and regulatory requirements. They facilitate site visits, perform source data verification, and serve as the primary point of contact for site personnel.
