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…