The Associate Medical Director provides medical expertise in the design, execution, and interpretation of oncology clinical trials. Key duties include collaborating on study protocols, providing medical oversight for safety and data, and maintaining relationships with regulatory authorities and key opinion leaders.
Remote Healthcare Jobs in Poland (66)
Remote in = Poland
Job category = Healthcare
The Clinical Lead II manages clinical delivery strategies, site start-up activities, and patient recruitment targets. They collaborate with project managers and sponsors to ensure study budgets and timelines are met while mitigating operational risks.
The Clinical Lead II manages clinical delivery strategies, site start-up activities, and patient recruitment and retention. They collaborate with project managers and sponsors to ensure study milestones are met and budgets are aligned with execution.
The role involves coordinating and monitoring clinical trials to ensure high-quality outcomes and patient safety. Key duties include managing study documentation, running sponsor queries, and maintaining relationships with clinical investigators and site staff.
The role involves coordinating and administering clinical trials while ensuring strict compliance with protocols and regulatory requirements. Key tasks include maintaining essential study documentation and collaborating with cross-functional teams to ensure smooth trial execution.
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The role involves coordinating and monitoring clinical trial activities to ensure high-quality outcomes and patient safety. Key tasks include managing study documentation, running sponsor queries, and maintaining relationships with clinical investigators and site staff.
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
Clinical Trials Associate - Europe
Worldwide Clinical Trials
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Full Time
·
4 Days Ago
Worldwide Clinical Trials
Provide administrative and project tracking support to the clinical project team to ensure tasks are performed accurately and timely. Responsibilities include managing system access, auditing project portals, and maintaining the trial master file.
The manager is responsible for evaluating, validating, and maintaining Digital Health data capture systems to support clinical trial activities. This includes leading project workstreams, documenting complex business requirements, and managing the DH governance framework.
The Principal Biostatistician leads the design, analysis, and interpretation of clinical studies, overseeing all contracted statistical outputs. They collaborate with cross-functional teams to develop protocols, statistical analysis plans, and summary reports while mentoring junior statisticians.
The Associate Biostatistician analyzes and interprets clinical trial data to support the design of statistical analyses and high-quality reports. They collaborate with clinical teams to validate methodologies and ensure data integrity for regulatory submissions.
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea
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Full Time
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1 Week Ago
Fortrea
Lead the full cycle of Clinical Data Management for oncology studies, serving as the primary point of contact for sponsors. Responsibilities include creating eCRFs, cleaning data, and managing vendor contracts and budgets.
Lead end-to-end clinical supply chain operations for international studies, including planning, forecasting, and distribution. Oversee key vendors and partner with internal stakeholders to ensure clinical materials are available and budgets are met.
Responsible for clinical data review, query resolution, and reconciliation to ensure data integrity and quality according to project timelines. May serve as an operational data management leader, assisting in the development of Data Management Plans and overseeing technical activities for small projects.
The Associate provides statistical capabilities and methodological support throughout all project stages, from planning to completion. Key tasks include drafting statistical protocols, performing sample size calculations, and developing statistical programs to generate analysis datasets and reports.
Associate Director, Operations - Clinical Assessment Technologies CAT) - UK/Europe - Remote
Worldwide Clinical Trials
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Full Time
·
1 Week Ago
Worldwide Clinical Trials
Oversee operational activities for Clinical Assessment Technologies (CAT) projects, including resource management and vendor oversight. Lead departmental initiatives, manage study deliverables from launch to close-out, and support business development activities.
Manage day-to-day clinical trial operations and lead RBM strategy meetings to develop site monitoring plans. Oversee site monitoring compliance, review visit reports, and partner with RBQM operations to ensure high-quality clinical outcomes.
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Design and conduct clinical studies to evaluate the safety and efficacy of innovative treatments, focusing on protocol development and regulatory documentation. Perform high-quality clinical data review and provide insights to improve data integrity and subject safety throughout the study lifecycle.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams for accurate data collection.
The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
The role involves designing and implementing clinical trial enrollment strategies while analyzing complex medical data for accuracy and compliance. The liaison acts as a primary point of contact between sponsors, investigators, and participants to optimize trial outcomes.
Manage and deliver full clinical site monitoring services, including the design and oversight of project monitoring, site recruitment, and regulatory filings. Act as a Lead CRA to mentor peers and serve as the primary liaison between the project team and sponsors.
FSP Clinical Trial Coordinator I
Thermo Fisher Scientific
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Full Time
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2 Weeks Ago
Thermo Fisher Scientific
Provides administrative and technical support for clinical trials, focusing on site activation, audit readiness, and eTMF maintenance. Coordinates trial activities, reviews investigator files, and liaises with sites to ensure regulatory compliance.
Clinical Research Associate 2 - Poland
Emerald Clinical Trials
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Full Time
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2 Weeks Ago
Emerald Clinical Trials
The CRA II is responsible for site management, monitoring activities, and operational support of clinical trials to ensure regulatory compliance. Key tasks include conducting site evaluation and initiation visits, managing site budgets, and training investigators on trial protocols.
Lead the statistical strategy and delivery for complex clinical trials, ensuring high-quality outputs and regulatory compliance. Provide strategic leadership, mentor junior statisticians, and act as a key advisor to cross-functional teams and clients.
Provide medical and therapeutic expertise to guide project teams and ensure clinical studies adhere to ethical and legal standards. Interact with sponsors and investigative sites to manage protocol issues and support business development efforts.
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Remotely evaluate asynchronous patient consultations and issue prescriptions for weight loss treatments, specifically GLP1s, for patients in Europe. Collaborate with the German-speaking customer support team to provide patient care via email, phone, or video.
The Medical Director oversees the execution of clinical trials in neuroimmunology, serving as the medical lead for assigned projects. Responsibilities include developing clinical development plans, overseeing medical writing for regulatory documents, and managing clinical teams.
Consulting Psychologist/Neurologist/Psychiatrist - Poland - MADRS Experience
Cogstate
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Full Time
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3 Weeks Ago
Cogstate
Remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects in pharmaceutical trials. Provide central monitoring by reviewing test batteries and recordings to ensure accuracy in administration and scoring.
Consulting Psychologist/Neurologist/Psychiatrist - Poland - Bayley Experience
Cogstate
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Full Time
·
3 Weeks Ago
Cogstate
Remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects and caregivers. Provide central monitoring by reviewing neuropsychological test batteries to ensure accuracy in administration and scoring.
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