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 IT Compliance Specialist will manage internal IT documentation, including change controls, risk assessments, and disaster recovery plans. They will also support internal and external audits by providing necessary documentation and addressing IT-related inquiries from 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, 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 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 CRA II acts as the primary liaison between the project team, sponsor, and clinical sites to ensure high-quality study conduct. Responsibilities include performing site selection, initiation, routine monitoring, and close-out visits while ensuring data integrity and compliance.
The Senior CRA manages communication with project stakeholders and maintains relationships with clinical sites to ensure research standards and timelines are met. Key duties include conducting onsite monitoring visits, performing data verification, and supervising study activities at the country level.
The Senior Clinical Research Associate will conduct onsite monitoring visits, manage site communications, and ensure data quality and compliance for clinical research projects. They will also supervise study activities, timelines, and support regulatory document preparation for various therapeutic indications.
The Medical Monitor provides medical input for global clinical studies and serves as the primary medical contact for project teams, sites, and sponsors. They are responsible for ensuring patient safety, reviewing clinical data, and ensuring compliance with regulatory guidelines such as FDA and EMEA.
Focus on compliance for in-house IT systems by creating and updating internal documentation such as risk assessments and disaster recovery plans. Support internal and external audits by providing documentation and participating in interviews.
The role focuses on managing compliance for in-house IT systems and processes to ensure adherence to industry standards and internal policies. Key duties include creating IT documentation, participating in audits, and conducting regular risk assessments.
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.
Contribute to the mission of expanding clinical trials to a broader range of sites and patients globally. Work within a fast-growing startup environment to build sustainable solutions for clinical research operations.
The role involves contributing to the mission of expanding clinical trials to a broader range of sites and patients globally. It focuses on building sustainable solutions within a fast-growing startup environment.
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.
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.
Provides clinical sites with technical support and expertise regarding study-related technologies such as imaging and radiology. Coordinates data collection, designs implementation guidelines, and organizes technical training for project teams.
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 Therapeutic Area Lead provides scientific and strategic expertise to develop PSI's Gastroenterology portfolio, specifically focusing on Inflammatory Bowel Disease. They partner with cross-functional teams to support business development, client engagement, and operational excellence in clinical studies.
Focus on compliance for in-house IT systems by creating and updating internal documentation such as change controls and risk assessments. Support internal and external audits by providing documentation and participating in interviews.
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.
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.
The role focuses on ensuring in-house IT systems and processes meet industry standards, internal policies, and regulatory requirements. Key tasks include creating IT documentation, managing audits, and conducting risk assessments to identify system vulnerabilities.
Join a global talent community to support the expansion of clinical trials to a broader range of sites and patients. Contribute to a fast-growing startup environment focused on operational excellence and sustainable solutions.
The Regulatory Officer prepares clinical trial dossiers for regulatory authorities and manages communications with stakeholders, sponsors, and vendors. They are also responsible for tracking legislative changes in Japan and delivering regulatory training to project teams.
The Director of Business Development is responsible for expanding the client base in the UK by prospecting new opportunities and cultivating long-term relationships with key decision-makers. They lead the entire sales process, from developing business plans and proposals to coordinating with operations for final pricing and strategy.
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 CRA II acts as the primary liaison between the project team, sponsor, and clinical sites to ensure high-quality study conduct. Responsibilities include performing site selection, initiation, routine monitoring, and close-out visits while ensuring data integrity and compliance.
Lead the clinical team by overseeing trial activities, ensuring high-quality execution, and maintaining compliance at a country or regional level. Coordinate cross-functional teams and provide mentorship and training to monitors while managing study risks and data integrity.
The Senior CRA manages communication with project stakeholders and maintains relationships with clinical sites and investigators. Responsibilities include conducting onsite monitoring visits, ensuring data compliance, and supervising study activities at the country level.
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.
Provides clinical sites with technical support and expertise regarding study-related technologies, including imaging and radiology. Coordinates data collection, organizes technical training, and assists in the design of study forms and manuals.
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.
Provides clinical sites with technical expertise and support regarding study-related technologies, including imaging and radiology. Coordinates data collection, designs technical guidelines, and organizes training for project teams.
Provides technical support and expertise to clinical sites regarding study-related technologies, including nuclear medicine and radiology. Coordinates data collection, organizes technical training, and assists in the design of study forms and manuals.
Lead and oversee clinical trial activities at a country or regional level, focusing on mentorship, oversight, and consistency in monitoring practices. Coordinate cross-functional teams to ensure high-quality execution, compliance, and timely delivery of study milestones.
The CRA II acts as the primary liaison between the project team, sponsor, and clinical sites to ensure high-quality study conduct. Responsibilities include performing site selection, initiation, routine monitoring, and close-out visits while ensuring data integrity and compliance.
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.
Prepare clinical trial regulatory submission dossiers and communicate with regulatory authorities, sponsors, and vendors. Deliver regulatory training to project teams and track legislative changes pertaining to clinical trials in Japan.
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.
The CRA II acts as the primary liaison between the project team, sponsor, and clinical sites to ensure high-quality study conduct. Responsibilities include performing site selection, initiation, routine monitoring, and close-out visits while managing data integrity and compliance.
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.
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.
The Site Technology Specialist provides technical support and expertise to clinical sites regarding study-related technologies and imaging procedures. They also coordinate data collection, organize technical training for project teams, and assist in the implementation of study-specific technical documentation.
The IT Compliance Specialist will manage internal IT documentation, including change controls and risk assessments, to ensure adherence to industry standards and policies. They will also support internal and external audits by providing necessary documentation and participating in IT-related interviews.
The IT Compliance Specialist will manage internal IT documentation, including change controls, risk assessments, and disaster recovery plans. They will also support internal and external audits by providing necessary documentation and addressing IT-related inquiries from stakeholders.
The IT Compliance Specialist will manage internal IT documentation, including change control and risk assessments, to ensure adherence to industry standards and policies. They will also support internal and external audits by providing necessary documentation and participating in interviews.
The IT Compliance Specialist will manage internal IT documentation, including change control, risk assessments, and disaster recovery plans. They will also support internal and external audits by providing necessary documentation and addressing compliance-related inquiries.
The Director of Business Development will be responsible for expanding the client base in the United Kingdom by actively prospecting, cultivating relationships with key decision-makers, and developing detailed business plans and sales strategies for target accounts. This role involves leading the entire sales process, from identifying opportunities and preparing presentations to coordinating proposal development and ensuring smooth hand-off to project teams.
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.
The Director of Business Development will expand the client base in the UK by prospecting new business opportunities and cultivating relationships with key decision-makers. They will lead the sales process, develop business plans, and ensure customer needs are met.
The Director of Business Development will be responsible for expanding the client base in the United Kingdom by actively prospecting, cultivating relationships with key decision-makers, and developing detailed business plans and sales strategies for target accounts. This role involves leading the entire sales process from identification of opportunities through to finalizing contracts and ensuring a smooth hand-off to the project team.
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.
