Review and evaluate technical and clinical documentation for active medical devices to ensure compliance with European and UK regulations. Manage certification activities for a portfolio of manufacturers and provide strategic regulatory support and mentoring.
Remote Healthcare Jobs in China (60)
Remote in = China
Job category = Healthcare
Responsible for conducting daily hospital visits, managing VIP relationships with hospital directors, and organizing product introduction meetings. The role involves territory planning, budget management, and executing product development strategies to meet sales targets.
The Medical Representative is responsible for conducting daily hospital visits, managing regional client relationships, and organizing product introduction meetings. They must also handle territory planning, financial budget management, and ensure consistent product knowledge through regular training and assessments.
The Medical Representative is responsible for conducting daily face-to-face visits with healthcare professionals to promote products and ensure high coverage of key accounts. They must also manage their assigned territory, track performance against targets, and handle financial budgeting for market activities.
The Medical Representative is responsible for managing a designated territory, conducting regular hospital visits, and organizing product presentations to healthcare professionals. They must also handle regional planning, budget management, and ensure consistent product knowledge through regular training and reporting.
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The Medical Representative is responsible for conducting daily hospital visits, managing key accounts, and organizing product presentations to healthcare professionals. They must also handle territory planning, budget management, and ensure consistent product knowledge through regular training and assessments.
The SVP leads the pharmacy strategy and field-based teams to deliver high-impact support and measurable value to strategic clients. This role involves managing executive-level relationships, driving organizational performance, and overseeing complex pharmacy solutions across the enterprise.
Provide medical safety expertise for clinical trials and post-marketing surveillance, including the review of adverse events and preparation of regulatory reports. Develop client relationships and provide safety support to project teams while ensuring compliance with global safety regulations.
The Senior Medical Science Liaison will serve as a scientific expert, fostering collaborative relationships with healthcare professionals and contributing to product strategy for SMA and ALS. They will facilitate scientific information exchange, support clinical trial investigator identification, and provide regional medical insights to internal teams.
Conduct on-site inspections and monitor loading processes according to operational procedures. Maintain communication with supervisors and suppliers while submitting daily reports and photos through the system.
The Senior Clinical Research Associate will monitor clinical trial sites to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards. They will also collaborate with cross-functional teams to ensure data integrity and provide training to site staff to maintain high standards of trial conduct.
You will manage day-to-day clinical trial operations, ensuring adherence to timelines, budget, and quality standards. You will also collaborate with cross-functional teams to implement protocols and manage relationships with investigators and stakeholders.
The inspector is responsible for conducting container loading inspections according to strict operational procedures and reporting findings daily. They must maintain clear communication with suppliers and supervisors while managing special situations effectively.
The Clinical Research Associate II is responsible for conducting site monitoring visits, ensuring protocol compliance, and maintaining data integrity throughout clinical trials. They also collaborate with investigators and site staff to facilitate study conduct and prepare essential study documentation.
MEDICAL INFORMATION SPECIALIST
Bracco Medical Technologies
·
Full Time
·
10 Weeks Ago
Bracco Medical Technologies
This role is within a contract type of Fixed Term at Bracco, an international healthcare group specializing in diagnostic imaging and contrast agents. The position is associated with Field Sales & Account Management, focusing on building client relationships and driving sales revenue.
Senior Clinical Data Manager
Precision Medicine Group
·
Full Time
·
11 Weeks Ago
Precision Medicine Group
The Senior Clinical Data Manager is responsible for managing all aspects of the clinical trial data management process from study start-up through post-database lock, ensuring adherence to SOPs and regulatory directives. This role involves leading data management activities, overseeing database development and testing, and ensuring data quality and timely delivery of milestones.
The Clinical Research Associate II implements and monitors clinical trials, ensuring sponsor and investigator obligations are met while adhering to local regulatory requirements and ICH GCP guidelines. Key duties include assessing sites, initiating and closing trials, reviewing data accuracy, providing status updates, and resolving trial-related issues.
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The Clinical Research Associate II implements and monitors clinical trials, ensuring sponsor and investigator obligations are met while adhering to local regulatory requirements and ICH GCP guidelines. Key duties involve assessing sites, initiating and closing trials, reviewing collected data, providing status updates, and resolving trial-related issues.
This posting is intended for a possible upcoming opportunity, adding interested candidates to a talent pipeline for future consideration as a Sr Clinical Trial Manager. The role involves working alongside industry experts to accelerate the delivery of important therapies to patients.
The role involves managing a network of Key Opinion Leaders (KOLs) to implement global programs locally, designing and executing country education plans, and serving as the subject matter expert for Dental Solutions products. This includes owning compliance aspects of Healthcare Professional (HCP) relationships and facilitating HCP training and scientific discussions.
The Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of allocated studies, ensuring compliance with ICH GCP. They must achieve the final clinical deliverable within the specified contractual time period while maintaining profitability and quality.
The Medical Representative is responsible for daily visits to clients, ensuring coverage and frequency for A and B level clients, and conducting monthly VIP visits to key hospitals. They must also organize weekly product presentations and manage their assigned territory effectively.
As a Care Provider, you will provide psychotherapy, counseling, and coaching sessions, lead support groups, and deliver Masterclasses. You will play an integral role in making high-quality care accessible to clients across the Asia-Pacific Region and Europe.
As a Quality Control Inspector, you will check emails for inspection documents, attend inspections on time, and communicate professionally with suppliers. You will also perform merchandise inspections and supervise container stuffing according to company procedures.
As a Quality Control Inspector, you will check emails for inspection documents, attend inspections on time, and communicate professionally with suppliers. You will also perform inspections and supervise the stuffing of containers according to company procedures.
The PEO Inspector is responsible for timely communication with suppliers and colleagues, conducting inspections according to operational procedures, and reporting findings. They will also assist colleagues with inquiries related to inspection images and reports.
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The Clinical Research Associate will contribute to the development of therapies that benefit patients by designing and delivering clinical trials. They will work in partnership with biopharmaceutical leaders and emerging innovators.
The Clinical Research Associate II implements and monitors clinical trials to ensure compliance with regulatory requirements and ICH GCP guidelines. They assess investigative sites, verify clinical trial data, and facilitate issue resolution while mentoring junior-level CRAs.
Conduct consultations both synchronously and asynchronously based on state telemedicine regulations. Provide care using a custom EMR, evaluating patient records, diagnosing, prescribing medication, and making lifestyle recommendations.
As a Clinical Specialist Consultant, you will ensure the reliability and standardization of assessments in clinical trials. Responsibilities include reviewing scales, conducting patient assessments, and evaluating rater performance.
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