execution, and close-out of clinical studies in accordance with ICH-GCP, local regulations, and company SOPs.
• Manage timelines, budgets, and resources, ensuring projects remain on track and within scope.
• Oversee site selection, start-up, monitoring...
Overview
Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA II) to join our A-team. As a CRA II at Allucent, you will independently control and monitor investigational sites, pro...
pipelines, introduce pragmatic AI solutions, and enable self‐service analytics that improve decision‐making across Clinical, R&D, Quality/RA, Operations, Finance/Controlling and IT.
Key Responsibilities
• Improve monitoring of clinical and research...
Functions:
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization...
devices. With Global Clinical Research Locations all over the world, OPIS offers a full range of integrated clinical research services as scientific advice, medical writing, trial start-up, monitoring, study management, data management, statistics...
a strong background in Data Management and trend analyses.
Key Responsibilities
Overall:
• Develop and implement comprehensive data governance frameworks.
• Monitor and ensure the quality, accuracy, and security of clinical trial data.
• Ensure full...
Job Overview
Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team...
Good Manufacturing Practice (GMP) regulations and regulatory authority requirements. This role oversees quality assurance for experimental products intended for clinical studies and contributes to ensure consistent quality and regulatory compliance...
Develop operational project plans
• Manage risk assessment and execution
• Responsible for management of study vendor
• Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables
Qualifications...
Job Summary :
The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those...
eccellente.
Per la nostra Unità Clinical Operations, siamo alla ricerca di una figura di Biometric Data Manager.
La risorsa si andrà ad occupare della gestione delle attività di Data Management relativa agli studi clinici.
Nello specifico, la risorsa...
and market trends.
Lead the development of feasibility studies and business plan and conduct assessments of healthcare organizations compared to their clinical and non-clinical operations
Develop and present high-quality deliverables, including reports...
digital biomarkers. Together they enable the continuous remote monitoring of human health across a range of conditions, through clinical-quality digital measurements.
Your ultimate call is to improve lives around the world, as part of a cross-functional...
Overview
Senior Manager, Talent Acquisition @ Allucent - let's connect for your career in clinical trials #CRO
The role
As a CRA II, you will take the lead on monitoring activities, owning your sites and relationships with investigators. You'll...