The Site Contract Specialist will review and negotiate site budgets and clinical trial agreements while coordinating the signature process. They will also maintain documentation in the Clinical Trial Management System and liaise with legal and project teams to support study startup activities.
The Site Contract Specialist will review and negotiate site budgets and clinical trial agreements while coordinating the signature process. They will also track negotiation status in the CTMS and maintain documentation within the Trial Master File.
The Clinical Research Associate will conduct onsite monitoring visits, manage site communications, and ensure data quality and compliance with study protocols. They will also support study startup activities, regulatory submissions, and oversee project timelines and schedules.
The CRA II will conduct onsite monitoring visits, manage site communications, and ensure data quality and compliance with clinical research standards. They will also support study startup activities, regulatory submissions, and oversee project timelines and site relationships.
The Clinical Project Manager will lead full-service clinical research projects in phases II and III, ensuring deliverables are met on time and within budget. Responsibilities also include mentoring project teams, supporting business development activities, and maintaining compliance with company standards.
The Site Contract Specialist will review and negotiate site budgets and clinical trial agreements while coordinating the signature process. They will also maintain documentation in the Clinical Trial Management System and the Trial Master File while liaising with legal and project teams.
The Clinical Project Manager will lead full-service clinical research projects in phases II and III, ensuring deliverables are met on time and within budget. They are also responsible for mentoring project teams, supporting business development activities, and maintaining compliance with company standards.
The Senior CRA is responsible for conducting onsite monitoring visits, performing source document verification, and ensuring data quality and compliance. They also manage site communications, oversee study timelines, and act as a primary point of contact for project stakeholders.
The Specialist Talent Acquisition leads the full cycle recruitment process, including sourcing, screening, and interviewing candidates for positions in the US and Canada. They also build candidate pipelines, maintain applicant databases, and advise hiring managers on industry talent trends.
The Specialist Talent Acquisition leads the full-cycle recruitment process, including sourcing, screening, interviewing, and extending offers to candidates. They also maintain applicant databases, build relationships with hiring managers, and provide analytical reports on recruitment progress.
The Senior CRA will conduct onsite monitoring visits, manage site communications, and ensure data quality and compliance with clinical research standards. They are responsible for driving study startup activities, verifying source documents, and supporting regulatory submissions.
The Clinical Research Associate will conduct onsite monitoring visits, perform CRF reviews, and manage site communications. They will also support project teams with study progress, feasibility research, and regulatory document preparation.
The Clinical Research Associate will conduct onsite monitoring visits, perform source document verification, and manage site communications. They will also support regulatory teams with study submissions and coordinate with internal project teams regarding study progress.
The Medical Monitor provides medical expertise and safety oversight for global clinical trials, acting as the primary point of contact for medical and safety-related inquiries. They are responsible for reviewing trial data, managing safety reports, and supporting clinical teams to ensure patient well-being and regulatory compliance.
The Trial Committee Manager oversees the end-to-end management of clinical trial committees, ensuring efficient and compliant execution of committee activities. They serve as the central point of coordination for sponsors, committee members, and cross-functional teams throughout the clinical trial lifecycle.
The Lead Project Manager is responsible for managing small to medium-sized clinical projects, ensuring they meet quality, timeline, and budget standards. Additionally, the role involves mentoring team members and supporting business development activities such as proposals and client presentations.
The Senior Project Manager leads project teams and manages medium to large-scale clinical research projects to ensure deliverables are met on time and within budget. They also act as a primary escalation point for clients and vendors while mentoring junior staff and supporting business development activities.
The Medical Monitor provides medical expertise and safety oversight for global clinical trials, acting as the primary point of contact for medical and safety-related inquiries. They are responsible for reviewing trial data, managing risks, and ensuring compliance with regulatory standards and study protocols.
The Medical Monitor provides medical input for global clinical studies while ensuring patient safety and regulatory compliance. They act as the primary point of contact for medical queries, manage trial risks, and support pharmacovigilance and data management teams.
The Lead Clinical Research Associate provides leadership, oversight, and mentorship for regional clinical trials while collaborating with project teams to ensure high-quality study execution. This role focuses on remote monitoring oversight, compliance, and data integrity rather than direct site management.
The Senior Clinical Research Associate will conduct on-site monitoring visits, manage site communications, and ensure data quality and compliance for clinical research projects. They will also oversee study timelines, support regulatory submissions, and act as a primary point of contact for project stakeholders.
The Regional Project Lead drives the successful delivery of clinical trials across multiple countries by managing project timelines, budgets, and site performance. They also mentor project teams, ensure compliance with industry regulations, and act as a primary point of contact for sponsors and cross-functional teams.
The Lead Clinical Research Associate provides leadership and oversight for clinical study teams, ensuring high-quality execution, compliance, and timely delivery of trial activities. They act as a primary coordinator across cross-functional teams, focusing on remote monitoring, mentorship, and project-level risk management.
The Lead Clinical Research Associate oversees clinical study teams, ensuring high-quality execution, compliance, and timely delivery of trial activities. They provide mentorship, manage project timelines, and act as the primary point of coordination across cross-functional teams.
The Lead Clinical Research Associate provides leadership and remote oversight for clinical study teams to ensure high-quality execution and compliance. They act as the primary coordinator across cross-functional teams, managing project timelines, data integrity, and site-level activities.
The Director of Business Development is responsible for expanding the client base in the US by prospecting new opportunities and cultivating long-term relationships with key decision-makers. This role leads the entire sales process, from developing business plans and proposals to coordinating with operations for final strategy and pricing.
The Regional Project Lead oversees and coordinates clinical trial activities across designated countries to ensure consistency in clinical operations and the meeting of study milestones. They manage project teams, ensure regulatory compliance, and serve as a primary contact for project management and support services.
Provide medical input and safety oversight for global clinical studies to ensure patient well-being. Act as the primary medical contact for regulatory authorities, IRBs, and trial teams while managing medical risks and reviewing clinical data.
Provide medical input and safety oversight for global clinical studies, acting as the primary contact for medical and safety-related queries. Responsibilities include monitoring participant safety, reviewing safety reports, and training trial teams on therapeutic protocols.
Provide medical input and safety oversight for global clinical studies, acting as the primary contact for medical and safety-related queries. Responsibilities include monitoring participant safety, reviewing safety reports, and training trial teams on therapeutic protocols.
Provide medical input and safety oversight for global clinical studies, acting as the primary contact for medical and safety-related queries. Responsibilities include monitoring participant safety, reviewing safety reports, and training trial teams on therapeutic protocols.
Provide medical input and safety oversight for global clinical studies, acting as the primary contact for trial-specific medical questions. Responsibilities include monitoring participant safety, reviewing safety reports, and training trial teams on therapeutic protocols.
The role involves maintaining databases, managing clinical research documentation, and serving as a communication point for investigative sites. Responsibilities also include coordinating query resolutions, arranging meetings, and preparing project agendas.
The role involves maintaining databases, managing clinical research documentation, and serving as a communication point for investigative sites. Responsibilities also include coordinating project training, resolving queries, and assisting with meeting arrangements.
Manages medium to large global clinical projects, ensuring deliverables meet quality standards, timelines, and budgets. Leads project teams and serves as the primary escalation contact for customers and vendors.
Manage small to medium-sized clinical projects ensuring deliverables meet quality standards, timelines, and budgets. Additionally, provide leadership through mentoring team members and assisting in business development tasks like proposal creation.
Manage small to medium-sized clinical projects ensuring deliverables meet quality standards, timelines, and budgets. Additionally, handle corporate assignments including team mentoring, feasibility research, and business development tasks.
Manages medium to large global clinical projects to ensure deliverables meet quality standards, timelines, and budgets. Leads project teams and serves as the primary escalation contact for customers and vendors.
The Senior CRA manages communication with project stakeholders and maintains relationships with clinical sites to ensure research standards and timelines are met. Responsibilities include conducting onsite monitoring visits, performing data verification, and supervising study activities at the country level.
Provide medical input and safety oversight for global clinical studies, acting as the primary contact for medical and safety-related queries. Responsibilities include monitoring participant safety, reviewing safety reports, and training trial teams on therapeutic protocols.
Lead and oversee clinical trial activities at a country or regional level, focusing on remote oversight, mentorship, and quality execution. Coordinate cross-functional teams to ensure compliance, data integrity, and timely delivery of project milestones.
The Senior CRA is responsible for conducting onsite monitoring visits and managing relationships with clinical sites and investigators. They ensure data compliance, subject safety, and the adherence of clinical research projects to timelines and standards.
Conduct and report on various types of onsite and remote monitoring visits for clinical studies. Manage site communication, perform CRF reviews, and assist in training less experienced CRAs.
Provide medical input and safety oversight for global clinical studies, acting as the primary contact for medical and safety-related queries. Responsibilities include monitoring participant safety, reviewing clinical study reports, and training trial teams on therapeutic protocols.
The Clinical Research Associate will conduct and report all types of onsite and remote monitoring visits, perform CRF review, source document verification, and manage site communication. Responsibilities also include involvement in site identification and potentially assisting in training less experienced CRAs.
The Clinical Research Associate will conduct and report all types of onsite and remote monitoring visits, perform CRF review, source document verification, and manage site communication. Responsibilities also include involvement in site identification and potentially assisting in training less experienced CRAs.
As a Clinical Research Associate, you will act as the main line of communication between the project team, sponsor, and site while ensuring quality standards in clinical studies. You will prepare and conduct monitoring visits, manage subject recruitment, and ensure compliance with study protocols.
