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 ensure high-quality data delivery for regulatory submissions.
The biostatistician collaborates with clinical investigators to design studies, develop protocols, and write statistical analysis plans. They are responsible for performing statistical analyses, ensuring participant safety through monitoring, and reporting findings for regulatory bodies and peer-reviewed journals.
The Director of Global Project Management provides oversight, guidance, and leadership to the clinical project management group to ensure successful delivery of biopharmaceutical clinical trials. They are responsible for managing project timelines, budgets, and client relationships while mentoring staff and driving operational efficiency.
The Clinical Research Associate II monitors clinical study sites to ensure trials are conducted in accordance with protocols, SOPs, and regulatory requirements. They perform site visits, verify source data, manage site documentation, and provide training to site staff under minimal supervision.
The Senior In-House CRA assists with operational activities, site management, and monitoring of clinical trials to ensure compliance with protocols and regulatory requirements. They also manage essential documentation, track trial progress, and provide mentorship to junior staff.
The Associate Director of Biostatistics will lead statistical efforts to advance clinical research across various therapeutic areas. They will collaborate with cross-functional teams to embed innovation into the company's clinical research processes.
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 Sr. Biostatistician leads collaborations with clinical investigators to design studies, develop statistical analysis plans, and perform complex statistical analyses. They also manage statistical activities for clinical studies, ensure scientific integrity, and represent the company at regulatory meetings.
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.
The Safety Manager implements Pharmacovigilance and Medical Monitoring activities while supervising safety monitors and contractors. They oversee the collection, assessment, and reporting of adverse drug reactions and ensure compliance with regulatory standards and safety monitoring plans.
The Project Leader serves as the matrix leader for government-sponsored clinical research projects, ensuring successful delivery within scope, timeline, and budget. They are responsible for managing client relationships, overseeing project quality, and coordinating across internal departments to mitigate risks and achieve project goals.
The Lead Biostatistician collaborates with investigators to design studies, develop protocols, and write statistical analysis plans. They perform statistical analyses, ensure data quality, and author scientific reports and publications.
The role focuses on managing strategic accounts in ophthalmology clinical trials to ensure value realization and long-term account expansion. Responsibilities include leading client onboarding, conducting governance meetings, and identifying growth opportunities in partnership with commercial teams.
Provides administrative support for the preparation and submission of regulatory packages for international clinical trials. Coordinates with cross-functional teams to track essential documents and maintain study timelines for site activation.
Provide lead statistical programming support for complex clinical research projects using advanced SAS techniques. Ensure regulatory-compliant output, develop programming documentation, and mentor junior staff.
The role involves administering and maintaining enterprise clinical applications to ensure high availability, security, and performance. Key duties include managing user access, implementing system upgrades, and collaborating with stakeholders to optimize application usage.
The Senior CRA is responsible for monitoring clinical study sites remotely and on-site to ensure trials are conducted according to protocols, SOPs, and ICH GCP guidelines. Key duties include conducting site visits, verifying source data, and managing action item resolution to ensure regulatory compliance.
The CRA II is responsible for monitoring clinical study sites remotely and onsite to ensure trials are conducted according to protocols, SOPs, and ICH GCP guidelines. Key duties include conducting site visits, verifying source data, and managing site staff training and compliance.
Oversee the delivery of global clinical trial operations by managing staff development, resource allocation, and operational efficiency. Act as a key escalation point to ensure quality, compliance, and financial management across projects.
The role provides lead oversight for statistical programming on complex clinical projects, ensuring timely delivery of regulatory submission deliverables. It involves managing staff, mentoring team members, and implementing standardized programming best practices.
Manage the end-to-end planning and execution of industry conferences and trade shows to enhance brand visibility. Convert event touchpoints into commercial opportunities through lead qualification and pipeline development for biopharma sponsors.
Lead proposal teams in developing high-quality, compliant biomedical research proposals for the U.S. government and other organizations. Manage the end-to-end proposal process, including shredding requirements, writing content, and coordinating with SMEs and pricing teams.
The Project Leader - Biostatistician serves as the matrix leader for government-sponsored clinical research projects, managing the core project team and ensuring delivery within timeline and budget. They are responsible for statistical leadership, client relationship management, and the continuous monitoring and mitigation of project risks.
Leads collaborations with clinical investigators to determine study design, develop protocols, and author statistical analysis plans. Manages statistical activities for clinical studies and presents findings in reports and peer-reviewed journals.
Oversees statistical activities and deliverables across a broad research area while managing a team of Biostatistician Managers. Serves as the primary statistical expert and client point of contact for large projects, ensuring high-quality and timely completion of deliverables.
The Associate Project Leader serves as the matrix leader for government-sponsored clinical research projects, ensuring deliverables are met within timeline and budget. They act as the primary point of contact for clients and stakeholders while coordinating across various internal departments to execute project goals.
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 site visits, conduct source data verification, and facilitate the resolution of action items while maintaining compliance with ICH GCP standards.
