Responsibilities: Prepare and submit regulatory dossiers for product registration, variations, renewals, and labeling approvals. Maintain up to date knowledge of local and international regulatory requirements (e.g., FDA, EMA, WHO, MHRA). Liaise with regulatory authorities to resolve queries and obtain approvals.…
Duties and Responsibilities ? Overall responsibility for daily clinical assessment and prescription of treatment for all patients attending the hospital. ? Identify and coordinate referral of patients for further management. ? Ensure proper documentation of patient notes. ? Improve patient…
Roles & Responsibilities of Drug Safety Associate or Pharmacovigilance Associate A Drug Safety Associate is a professional who works in the field of pharmacovigilance within a pharmaceutical, biotechnology, medical company or life sciences consulting firm. The main role of a…
As a pharmacologist, you'll need to: design, plan and conduct controlled experiments and/or clinical trials to improve understanding of a drug's activity collect, analyse and interpret data using computers, high technology measuring systems and other sophisticated equipment make recommendations based…
Medical Coder Job Responsibilities: Accounts for coding and abstracting of patient encounters, including diagnostic and procedural information, significant reportable elements, and complications. Researches and analyzes data needs for reimbursement. Analyzes medical records and identifies documentation deficiencies. Serves as resource and…
Clinical Research Coordinator Responsibilities and Duties Coordinate and manage clinical trial activities from initiation to close out Recruit, screen, and enroll study participants according to protocol criteria Obtain informed consent and ensure participant understanding Schedule and conduct study visits, procedures,…
Regulatory Affairs Specialist duties and responsibilities Ensuring compliance with all regulatory requirements Maintaining regulatory documentation database Assisting with the preparation and submission of all regulatory reports Providing accurate reviews of data and reports Ensuring accurate and timely submissions to regulatory…
Higher level science courses including anatomy and physiology Focus on pursuing a career in healthcare at a graduate/doctorate level Prior experience in healthcare settings, particularly in the role of medical scribe Knowledge of medical terminology Understanding of medical note content,…
Responsibilities Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case…
Higher level science courses including anatomy and physiology Focus on pursuing a career in healthcare at a graduate/doctorate level Prior experience in healthcare settings, particularly in the role of medical scribe Knowledge of medical terminology Understanding of medical note content,…
Responsible for review of investigational new drug safety reports (INDSR) and submission to FDA (as applicable) Responsible for negotiation and implementation of pharmacovigilance agreements (PVA) with business partners Supports PV Clinical Specialists in tasks and projects as needed Responsible for…
Responsibilities for clinical data management Identifies ways to continuously improve all aspects of data management and implements solutions Support the team in their communication with stakeholders Support the Clinical Programmer(s) in their key responsibilities Under supervised training and mentoring, gradually…
Responsibilities Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case…
Medical Coder Responsibilities: Extracting relevant information from patient records. Liaising with physicians and other parties to clarify information. Examining documents for missing information. Ensuring documents are grammatically correct and free from typing errors. Performing chart audits. Advising and training physicians…
The mission of the Regulatory Affairs Specialist (RAS) is to prepare and file demands for regulatory approval of the products of one’s company. Biotechnology companies, which have lesser means than large pharmaceutical companies, prioritize experienced candidates or else turn to…
As a pharmacologist, you'll need to: design, plan and conduct controlled experiments and/or clinical trials to improve understanding of a drug's activity collect, analyse and interpret data using computers, high technology measuring systems and other sophisticated equipment make recommendations based…
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…
Roles and Responsibilities Write and edit high quality medical journals, abstracts, white papers, articles, brochures, regulatory documents, and product manuals about healthcare related topics such as [new medicinal discoveries/treatments, educational materials, clinical research, and product instructions]. * Communicate with medical…
A Clinical Research Coordinator is responsible for a variety of duties including the following: Overseeing the trouble free running of clinical trials Collecting data obtained from research, coding and analyzing it Managing budgets set aside for research Communicating with participants…
Job description Correspond or meet with providers to resolve abusive billing practices and to reach an appropriate financial settlement Educate providers on plan policies and guidelines, medical necessity criteria, UM programs correct billing methods and procedure codes by written and…