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 In-House Clinical Research Associate assists with operational activities, site management, and monitoring of clinical trials to ensure compliance with protocols and regulatory requirements. They are responsible for maintaining essential documents, tracking trial progress, and coordinating with internal and site staff to resolve issues.
The Payroll Specialist manages end-to-end payroll operations across multiple countries while ensuring compliance with local labor laws and tax regulations. They act as a subject matter expert, collaborating with HR and Finance teams to maintain accurate records and reporting.
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 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 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 Senior Clinical Research Associate 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, verify source data, and facilitate site compliance and action item resolution.
The Global Project Manager leads biopharmaceutical clinical trials as a matrix leader, ensuring projects are delivered on time, within budget, and to high quality standards. They serve as the primary client contact, managing project resources, risks, and stakeholder relationships throughout the study lifecycle.
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 Senior Clinical Research Associate monitors clinical study sites remotely or on-site to ensure compliance with protocols, SOPs, and regulatory requirements. They facilitate site visits, conduct source data verification, and serve as the primary point of contact for site personnel.
The Biostatistician collaborates with clinical investigators to design studies, develop protocols, and write statistical analysis plans. They are responsible for performing statistical analyses, ensuring data quality, and reporting findings to internal and external stakeholders.
The Principal Statistical Programmer provides lead programming support for complex clinical research projects and offers expert consultation on methodologies. They are responsible for delivering regulatory-compliant outputs, developing documentation, and mentoring junior staff.
The Study Startup Associate II provides administrative support for regulatory submission packages and manages study timelines for international clinical trials. They are responsible for tracking essential documents, coordinating with cross-functional teams, and ensuring regulatory compliance across investigational sites.
The Customer Success Manager will lead strategic account management, overseeing onboarding and value delivery for global ophthalmology clinical trial sponsors. They will also drive account growth by identifying expansion opportunities and collaborating cross-functionally to ensure operational excellence.
The Project Leader serves as the matrix leader for government-sponsored clinical research projects, ensuring successful delivery within timeline and budget. They manage cross-functional teams, oversee project quality, and act as the primary point of contact for clients and stakeholders.
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 Senior Biostatistician leads collaborations with clinical investigators to design studies, develop statistical analysis plans, and perform statistical inferences. They also manage statistical activities for clinical studies and oversee the development of study reports and scientific 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.
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 fostering collaborative relationships with contract sponsors and project teams.
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.
The Computational Biologist will design and implement AI/ML models for biomedical data analysis to support precision oncology and translational research. They will also curate and integrate complex datasets while generating actionable scientific reports for stakeholders.
