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.
PSI CRO
67 Remote Job Openings at PSI CRO
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.
Oversees the operational conduct of clinical trials at contracted medical institutions and provides leadership to Site Coordinators. Responsible for assessing protocol feasibility, monitoring budget negotiations, and driving process standardization in alignment with regulatory requirements.
Oversees the operational conduct of clinical trials at contracted medical institutions and provides leadership to Site Coordinators. Responsible for assessing protocol feasibility, monitoring budget negotiations, and driving process standardization in alignment with ICH GCP.
Oversees the operational conduct of clinical trials at contracted medical institutions and provides leadership to Site Coordinators. Focuses on staff development, process standardization, and ensuring adherence to ICH GCP and regulatory requirements.
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.
Lead and develop a team of Clinical Research Associates while overseeing operational efficiency and resource utilization. Ensure the successful delivery of clinical trials through quality control, audit participation, and cross-functional collaboration.
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.
Medical Monitor (Canada Board-Certified Gastroenterologist)
PSI CRO
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Full Time
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17 days ago
PSI CRO
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 Proposal Manager coordinates all phases of the proposal process, from RFP strategy to bid defense slide decks. They partner with global subject matter experts to produce competitive budgets and strategic proposals to maintain a high win rate.
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.
Facilitate the negotiation of site agreements and budgets to align with activation plans. Manage the preparation, signature process, and filing of executable site agreements in the Trial Master File.
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.
The Director of Business Development is responsible for expanding the client base in North America 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 pricing and strategy.
Medical Monitor (Canada Board-Certified Gastroenterologist)
PSI CRO
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Full Time
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25 days ago
PSI CRO
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 Proposal Manager coordinates all phases of the proposal process, from RFP strategy to bid defense slide decks. This includes developing competitive budgets, writing strategic proposals, and collaborating with global subject matter experts to maintain a high win rate.
This role focuses on the leadership, mentorship, and remote oversight of monitoring practices to ensure study quality and compliance. Key duties include coordinating site feasibility, managing project timelines, and supervising the project team in contracting and payments.
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.
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.
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 Regional Project Lead oversees and coordinates clinical trial activities across designated countries to ensure consistency in operations and meeting of study milestones. They manage project teams, ensure regulatory compliance, and handle site contractual startup and budget negotiations.
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.
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. They lead the entire sales process, from developing business plans and proposals to coordinating with operations for final pricing and strategy.
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.
Responsible for building and optimizing infrastructure, CI/CD pipelines, and deployment processes across multiple environments. This includes managing containerized environments in AKS and implementing monitoring and observability solutions.
Responsible for building, maintaining, and optimizing infrastructure, CI/CD pipelines, and deployment processes across multiple environments. This includes managing containerized environments in AKS and implementing monitoring and observability solutions.
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.
Clinical Research Associate / Senior Clinical Research Associate
PSI CRO
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Full Time
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2 months ago
PSI CRO
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 Regional Project Lead oversees clinical trial activities across designated countries to ensure study milestones and enrollment targets are met. They manage project teams, ensure compliance with industry regulations, and coordinate site startup, monitoring, and reporting processes.
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 Director of Business Development will be responsible for expanding the existing client base in the United States 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, coordinating proposal development, handling contractual follow-up, and ensuring a smooth knowledge transfer to the project team.
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.
Clinical Research Associate / Senior Clinical Research Associate
PSI CRO
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Full Time
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5 months ago
PSI CRO
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.
The Director of Business Development will expand the existing client base in the United States by actively prospecting and leveraging new business opportunities. This role involves cultivating relationships with key decision-makers and leading the entire sales process, including presentations and proposal development.
The Lead Clinical Research Associate coordinates site feasibility and study startup, monitors project timelines, and manages communication between various stakeholders. They also conduct monitoring visits, oversee data integrity, and ensure compliance with regulatory guidelines.
