Job description: -Identifying potential clients through market research, networking, and referrals.  -Developing and executing strategies to attract and convert prospects into clients.  -Creating and delive...

A medical coder is someone in an administrative position within the healthcare industry. They are responsible for translating details from a patients medical documents into medical codes to ensure the patients records are acc...

A SAS analyst's primary role is to use the SAS software to analyze and interpret complex datasets, extracting meaningful insights to support business decision-making. They are responsible for data extraction, transformation, ...

Drug safety specialists are leading players in a field known as pharmacovigilance that is, the science of collecting, detecting and preventing adverse effects (AEs) in patients who take new drugs and other pharmaceutical prod...

The Clinical Data Analytics & Reporting Programmer, within the CDA&R team, will be responsible for interpretation and translation of clinical data review needs into technical specifications, aggregation of data source...

Clinical researchers work in the healthcare or health sciences industries to develop new technologies, medications and treatments. If you're interested in science or biomedical research and enjoy tracking data and resear...

Position: Medical Coder Ct: HR DEEPA - 7305649640:Position: Medical Coder.Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medical reports from doctor...

As a health and safety Manager, you'll need to: Carry out risk assessments and consider how risks could be reduced Outline safe operational procedures which identify and consider all relevant hazards Carry out regular site...

They manages the day-to-day operations of a clinical trial, ensuring participant safety, data accuracy, and protocol adherence. They are responsible for recruiting and screening participants, obtaining informed consent, colle...

 Their responsibilities include reviewing safety data, identifying potential safety signals, assessing causality, and providing guidance on risk management and communication.  Key Responsibilities:  Safety ...

A Clinical Data Coder translates clinical trial data into a standardized format using coding dictionaries like MedDRA and WHODD. They review clinical documentation, assign appropriate codes, and ensure data integrity and com...

 Regulatory medical writers play a significant role in preparing documents and ensuring that they are accurate, concise, and compliant with the prevalent standards. Summarizing safety and/or efficacy data for a CSR R...

Roles and responsibilities: create, conduct and monitor experiments using live organisms or biomolecular processes in a laboratory setting to solve problems, improve processes and develop new products. perform data analys...

Primary role involves reviewing patient charts, identifying diagnoses and procedures, and assigning the appropriate codes according to established coding systems like ICD-10, CPT, and HCPCS. Analyzing patient charts, inclu...

Roles and Responsibilities Data Collection and Management: Receive, catalog, and manage large volumes of adverse event reports.  Reporting: Report adverse events and safety concerns to regulatory authorities, ensurin...

A Clinical Research Analyst is responsible for collecting, analyzing, and reporting on clinical data to support research studies and trials. They work closely with researchers, doctors, and other healthcare professionals to e...

should have hands on experience in handling HPLC, GC, LC-MS/MS instruments independently. Should have analytical method development & validation exposure. Experienced in Nitrosamines analysis and E&L exposure a plus. Good ...

Responsibilities: Medical Record Review: Analyzing patient medical records for completeness, accuracy, and compliance with regulatory standards. Identifying gaps or inconsistencies in documentation. Physician Que...

Responsibilities: Review CRFs to ensure consistency with protocol and adequacy to collect the data to meet the objectives defined in the statistical section of the protocol. Develop and maintain comprehensive Data Managem...

Roles and Responsibilities Adverse event collection and reporting: Receiving and reviewing adverse event reports from healthcare professionals, clinical trials, and other sources.  Case processing: Performing detaile...

Responsibilities: Design and build eCRFs within Medidata Rave, ensuring adherence to protocol and data standards. Develop and maintain comprehensive Data Management Plans. Perform data validation and quality checks, reso...

Responsibilities:Detailed Duties: List of specific responsibilities, including: Conducting site initiation, monitoring, and close-out visits. Ensuring compliance with GCP, ICH guidelines, and regulatory requirements. ...