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The Clinical Research Associate is responsible for conducting remote and on-site monitoring visits to ensure data integrity and patient safety. They also manage clinical study documentation, including the Trial Master File, in accordance with ICH/GCP guidelines and sponsor requirements.
You will be responsible for all site management and supervisory activities for assigned oncology studies. Additionally, you will mentor junior CRAs and work with industry leaders to ensure successful clinical trial execution.
The IPOST Clinical Community Analyst manages investigator portals throughout the clinical trial lifecycle, from start-up to archiving. They partner with study teams to implement site engagement strategies, create portal content, and facilitate effective communication with site personnel.
The Senior Clinical Trial Manager provides leadership and direction to clinical site management teams while overseeing regional CTMs and coordinating study activities. They are responsible for developing monitoring strategies, managing budgets, and ensuring compliance with clinical protocols and regulatory requirements.
The Medical Director will provide strategic medical leadership and scientific guidance across project teams to ensure high-quality medical affairs delivery. They are responsible for maintaining regulatory compliance, overseeing safety monitoring activities, and representing the department in business development initiatives.
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The Medical Director will provide expert medical guidance to project teams and ensure clinical studies adhere to ethical and legal standards. They will also oversee safety data reviews, contribute to study documentation, and support business development efforts.
The Senior Clinical Scientist will design and conduct clinical studies to evaluate the safety and efficacy of innovative treatments while providing strategic leadership for clinical programs. They will also author clinical protocols, study reports, and regulatory submissions in collaboration with cross-functional teams.
The Manager Clinical Operations oversees, trains, and coaches a team while managing performance through metrics and key performance indicators. They also collaborate with leadership on resourcing, ensure adherence to regulatory standards, and support project deliverables.
The Senior CRA monitors clinical studies at investigative sites or remotely to ensure compliance with protocols, SOPs, and regulatory requirements. They are responsible for site qualification, initiation, monitoring, and close-out visits while maintaining productive relationships with site staff.
Lead and oversee complex clinical trial start-up activities across multiple EU countries while ensuring adherence to regulatory requirements and project timelines. Manage cross-functional stakeholders, site activation processes, and financial/contractual aspects to ensure successful study delivery.
The Clinical Payments Specialist manages end-to-end global investigator payments, including setup, deployment, and reconciliation of study payment solutions. They act as a liaison between investigative sites and clinical teams while ensuring payments align with clinical trial agreements and budgetary forecasts.
The Senior Biostatistician will lead biostatistics tasks, including designing clinical trials, developing statistical analysis plans, and interpreting complex medical data. They are responsible for ensuring technical depth, quality, and continuous improvement across all assigned clinical studies.
The Clinical QA Manager is responsible for ensuring robust oversight of clinical trial compliance at the country and site level using a risk-based approach. They will coordinate quality assurance strategies, conduct audits, and collaborate with stakeholders to safeguard patient safety and data integrity.
The Clinical Research Associate is responsible for managing clinical site relationships, ensuring protocol compliance, and overseeing the quality and integrity of clinical trial data. They will conduct site visits, develop patient recruitment strategies, and act as the primary point of contact for clinical sites.
The Clinical Quality Associate Director ensures clinical studies meet high standards of quality, compliance, and integrity by acting as a trusted advisor to local and global teams. They drive risk management, support audit and inspection readiness, and lead operational improvement initiatives to ensure efficient clinical trial delivery.
The Senior Clinical Pharmacologist will lead clinical pharmacology strategies across early and late-phase drug development programs while partnering with cross-functional teams to drive decision-making. They will apply model-informed drug development principles to support dose selection, biomarker optimization, and regulatory submissions.
The Associate Director leads the global Health & Safety strategy by developing governance frameworks, compliance programs, and risk management methodologies. They partner with regional leadership to embed safety as a core value while driving continuous improvement through data analytics and standardized policies.
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Provide leadership for clinical data management projects, including oversight of vendor performance, budgets, and strategic planning. Act as the primary point of contact for clinical data management while ensuring compliance with industry standards and study protocols.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to pediatric subjects and their caregivers. They will also perform central monitoring by reviewing test data to ensure accuracy and providing feedback to other raters.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects. They are also responsible for scoring assessments and providing central monitoring reviews to ensure data accuracy.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to pediatric subjects and caregivers. They will also provide central monitoring of neuropsychological test batteries to ensure data accuracy and provide feedback to other raters.
The Clinical Research Associate II is responsible for monitoring clinical study sites to ensure trials are conducted in accordance with protocols, SOPs, and regulatory requirements. They perform remote and on-site monitoring visits, manage site documentation, and facilitate communication between site personnel and the project team.
You will oversee clinical trial management workstreams, ensuring all deliverables meet quality, timeline, and regulatory standards. This includes collaborating with cross-functional teams to implement protocols, manage budgets, and optimize study outcomes through data analysis.
The Director will serve as the primary point of contact for sponsors and CROs across Central and Eastern Europe to ensure effective study launches and site performance. They will manage stakeholder relationships, report on study progress, and drive regional network growth by maintaining high standards of service delivery.
The Senior Clinical Data Manager will oversee the end-to-end clinical data management process, including study setup, database maintenance, and reconciliation. They are responsible for leading study teams, managing vendor deliverables, and ensuring data accuracy and compliance with protocol requirements.
The Medical Director will provide expert medical monitoring and leadership for clinical research projects, ensuring compliance with protocols and safety standards. They will also support business development, mentor junior staff, and maintain strong consultative relationships with clients.
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The incumbent will lead medical science and strategy for metabolic clinical research, providing expert input on development plans, regulatory issues, and clinical trial protocols. They will also engage in business development, support client proposals, and mentor internal clinical teams to ensure high-quality delivery of research projects.
The incumbent will lead medical science and strategy for oncology, driving business outcomes through proposal development, client engagement, and strategic clinical trial design. They will also provide therapeutic expertise to internal teams, mentor clinical scientists, and contribute to innovative clinical research initiatives.
The Clinical Specialist reviews clinical trial data and assessment scales to ensure standardized practices and data integrity. They also conduct live interactions with raters to provide guidance on methodology, scoring techniques, and performance support.
The role involves leading clinical trial start-up activities, including site activation and the preparation of essential regulatory documents. You will collaborate with cross-functional teams to streamline processes and provide guidance to study teams to ensure compliance and project success.
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