The Senior Site Activation Specialist is responsible for managing site activation activities within clinical trials to ensure project timelines are met. They collaborate with cross-functional teams to navigate complex regulatory environments and accelerate the drug development process.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams to manage site visits, track study progress, and maintain accurate documentation.
The lead statistical programmer will develop custom code to generate clinical trial outputs and ensure compliance with regulatory standards. They will also direct programming activities, mentor junior staff, and serve as a technical subject matter expert for CDISC and regulatory requirements.
The Site Management Associate will collaborate with clinical teams to manage site activities and ensure adherence to drug development protocols. They are responsible for navigating complex clinical environments to support customer goals and patient progress.
The Principal Statistical Programmer develops custom code to generate summary tables, listings, and graphs while ensuring quality standards and regulatory compliance. They also act as a lead programmer, directing team activities and providing technical expertise on CDISC standards and clinical drug development.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Senior CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and ensure the safety and integrity of clinical study data.
Responsible for site management oversight, clinical monitoring, and ensuring protocol/GCP/regulatory compliance and data integrity. Collaborates with functional leaders to coordinate study milestones and manages clinical project team deliverables including risk mitigation.
The Senior CRA I performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support subject safety and data integrity throughout the study lifecycle.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
Leads the preparation and completion of complex regulatory medical writing deliverables while ensuring scientific accuracy and adherence to regulatory standards. Coordinates cross-functional reviews and provides mentorship to less experienced writers to ensure project timelines and quality requirements are met.
The Clinical Data Reviewer performs specialized clinical review of study data to ensure readiness for milestones such as interim analysis and regulatory submissions. They work closely with clinical scientists to identify data inconsistencies, raise queries, and assess the scientific validity of participant data.
The role involves providing strategic direction for clinical trials, managing high-tier client relationships, and overseeing a complex portfolio of research projects. It also requires financial accountability, talent development, and driving organizational innovation within the clinical solutions team.
The role involves providing strategic direction for clinical trials, managing high-stakes client relationships, and overseeing the financial and operational health of a complex portfolio. The incumbent will also lead organizational initiatives, mentor senior project leaders, and ensure high-quality project delivery across neurodegenerative research programs.
The role involves providing strategic direction for clinical trials, managing high-stakes client relationships, and overseeing a complex portfolio of research projects. It also requires driving business development, ensuring financial health, and fostering a culture of quality and innovation across the organization.
The role involves providing strategic direction for clinical trials and serving as a senior-level advisor for top-tier clients. Responsibilities include overseeing project delivery, managing financial health, and fostering organizational growth through business development and leadership.
The Senior Talent Acquisition Specialist serves as a strategic partner to hiring managers, managing the full-cycle recruitment process from sourcing to onboarding. They are responsible for developing hiring strategies, maintaining market knowledge, and ensuring a collaborative, efficient recruitment experience.
Acts as the functional lead for data management, coordinating project teams and ensuring all data activities meet contractual and regulatory standards. Manages project plans, documentation, and resource allocation while facilitating communication between internal and external stakeholders.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA I performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The consultant will provide regulatory CMC expertise for small molecule products while utilizing Veeva RIM systems. They are responsible for navigating regulatory frameworks, maintaining product market compliance, and contributing to drug development projects.
The Clinical Data Reviewer will collaborate with cross-functional teams to manage clinical data and support drug development processes. They are responsible for applying deep expertise to understand customer needs and delivering high-quality solutions within a competitive environment.
Conduct site qualification, initiation, monitoring, management, and close-out activities while ensuring compliance with protocols, regulations, and Good Clinical Practice. Review clinical records and study data, manage site documentation and investigational products, resolve issues, support recruitment and audit readiness, and coordinate with study teams and site personnel.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and escalate serious issues to the project team.
Support the preparation, customization, execution, and filing of confidentiality disclosure agreements, clinical study agreements, budgets, and vendor agreements. Track contract-related documents, site intelligence, and metrics, and contribute to updates to playbooks and templates while communicating potential process improvements.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Clinical Trial Manager II is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity. They coordinate with functional teams to meet study milestones, manage risks, and oversee the performance of CRAs and Central Monitors.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain investigator site files throughout the study lifecycle.
Perform site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and maintain investigator site files while supporting patient recruitment and retention.
