The Site Contract Specialist facilitates the negotiation of site agreements and budgets to ensure alignment with activation plans. They also manage the preparation, translation, and filing of legal documents within the Trial Master File.
The Site Budget Specialist will review and negotiate site budgets and clinical trial agreements while maintaining documentation in the CTMS. They will also coordinate the signature process for contracts and liaise with legal and project teams to support study startup activities.
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 Site Budget Specialist will review and negotiate site budgets and clinical trial agreements while coordinating with legal and project teams. They are responsible for tracking negotiation status in the CTMS and maintaining accurate documentation for executed contracts.
The Site Budget Specialist will review and negotiate site budgets and clinical trial agreements while maintaining documentation in the Clinical Trial Management System. They will also coordinate the signature process for contracts and liaise with legal and project teams to support study startup activities.
The role involves facilitating the negotiation of site agreements and budgets to align with activation plans. Additionally, the coordinator will prepare executable versions of contracts and maintain documentation within the Trial Master File.
The Clinical Research Associate is responsible for conducting monitoring visits, ensuring compliance with study protocols and regulatory guidelines, and maintaining accurate site documentation. They will also build relationships with investigators, oversee trial supplies, and manage site-level risks to ensure high-quality clinical research.
The Talent Acquisition Specialist will manage end-to-end recruitment across Europe, including sourcing, screening, and interviewing candidates. They will also partner with hiring managers to understand business needs and maintain the Applicant Tracking System.
The Lead Software Developer oversees the full lifecycle of software projects while providing technical mentorship to engineering teams. They are responsible for architecting applications, ensuring technical quality, and collaborating with cross-functional teams to meet business requirements.
You will architect, develop, and maintain business applications while processing user requests for new features. Additionally, you will be responsible for preparing documentation, executing software tests, and participating in code reviews.
You will architect, develop, and maintain business applications while processing user requests for new features. Additionally, you will perform software testing, participate in code reviews, and maintain documentation for internal IT systems.
The Clinical Research Associate will conduct on-site monitoring visits, ensure data quality, and manage relationships with clinical sites and investigators. They are also responsible for overseeing study timelines, regulatory document preparation, and site communication.
The Clinical Research Associate will conduct onsite monitoring visits, perform CRF reviews, and ensure quality standards across various clinical studies. They will also manage site communications, support regulatory submissions, and participate in audits and inspections.
The role involves facilitating the negotiation of site agreements and budgets to ensure alignment with activation plans. Additionally, the specialist will prepare and customize site-specific agreements while maintaining accurate records in the Trial Master File.
The Senior CRA is responsible for conducting onsite monitoring visits, managing clinical sites, and ensuring data quality and compliance with study protocols. They also act as a primary point of contact for stakeholders and support regulatory document preparation.
The Clinical Research Associate will conduct onsite monitoring visits, perform CRF reviews, and manage site communications to ensure study quality. They will also support regulatory teams with document preparation and participate in feasibility research and audits.
Serve as a key contact for investigative sites, supporting day-to-day study delivery, resolving site questions, coordinating training and systems access, and tracking activities and follow-ups. Maintain accurate study records and documentation, coordinate communication across stakeholders, and support project meetings by preparing agendas, recording minutes, and following up on actions.
Build and manage a country-specific network of referring physicians, providing training, support, and regular visits to promote effective referrals to study investigators. Document discussions and objectives, follow up on agreed tasks, and collaborate with Clinical Operations, Regulatory, and Legal teams to implement referral processes across projects.
Build and manage a country-specific network of referring physicians, providing training, support, and regular visits to promote effective collaboration with study investigators. Document discussions and objectives, support completion of agreed tasks, and coordinate with Clinical Operations, Regulatory, and Legal teams to implement referral processes across projects.
The Clinical Research Associate acts as the primary liaison between the project team and clinical sites to ensure study conduct meets quality and regulatory standards. Responsibilities include performing site monitoring visits, managing data integrity, and overseeing the accountability of investigational products.
The Clinical Trial Liaison acts as a specialized point of contact to assist clinical sites with patient identification, recruitment, and retention strategies. They also provide protocol-specific support to site teams and ensure accurate documentation of study-related assessments.
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 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 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 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 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 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 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 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.
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.
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.
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.
