Responsibilities: Support clinical research teams with trial documentation and coordination. Maintain accurate and up to date study files and records. Assist with the preparation and organization of trial documentation. Ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.…
Responsibilities Developing and writing clear and concise medical documentation in accordance with industry guidelines Reviewing and editing documents created by other team members or external vendors Ensuring all documentation meets regulatory requirements and is submitted on time Collaborating with cross…
Responsibilities: Document all physician patient interactions in real time during consultations. Accurately update patient information in the Electronic Health Records (EHR) system. Prepare and organize patient charts prior to appointments. Retrieve diagnostic test results, lab work, and imaging records for…
Key Responsibilities: Research and Analysis: Conduct experiments to study microorganisms (bacteria, viruses, fungi, etc.) in controlled laboratory settings. Investigate the interactions between microorganisms and human/animal/plant systems. Perform genetic, biochemical, and microbiological analyses of samples. Develop methods for isolating, identifying, and…
Clinical Research Associate Responsibilities: Creating and writing trial protocols, and presenting these to the steering committee. Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial. Training site staff on therapeutic areas, protocol requirements, proper…
Responsibilities: Monitor and evaluate adverse drug reactions (ADRs) from clinical trials and post marketing surveillance. Ensure compliance with regulatory guidelines for drug safety reporting. Prepare and submit safety reports to regulatory authorities. Collaborate with healthcare professionals to assess and manage…
Responsibilities Develop and implement data management plans for clinical trials Ensure data quality and integrity throughout the trial Develop and maintain study specific data management documents such as data management plans, annotated CRFs, and database specifications Collaborate with cross functional…
Key Responsibilities: Assist in recruitment, onboarding, and employee records management Coordinate training and development programs based on organizational needs Schedule, organize, and track training sessions, workshops, and seminars Collaborate with department heads to identify skills gaps and development opportunities Maintain…
Responsibilities: Monitor and evaluate adverse drug reactions (ADRs) from clinical trials and post marketing surveillance. Ensure compliance with regulatory guidelines for drug safety reporting. Prepare and submit safety reports to regulatory authorities. Collaborate with healthcare professionals to assess and manage…
Key Responsibilities: Review Patient Records: Examine clinical documents, including physician notes, lab reports, and test results, to determine the correct medical codes. Code Diagnoses and Procedures: Apply ICD 10 codes for diagnoses and CPT/HCPCS codes for procedures to ensure correct…
Key Responsibilities: Study Planning & Preparation: Assist in the development of study protocols, informed consent documents, and other study related documents. Collaborate with Principal Investigators (PIs) and other clinical staff to ensure the research study is ready for initiation. Ensure…
Medical Scribe Responsibilities: Transcribe patients' medical histories. Record medical examination findings. Digitize patient records. Greet patients and introduce them to healthcare professionals. Keep abreast of industry innovations. Medical Scribe Requirements: A bachelor's degree in healthcare. Proficiency with Microsoft Office. Excellent…