Clinical Research Monitor-TIPS-3 PHRI Study

Job DescriptionRoles and Responsibilities:Site Coordination- Assist senior team members in the coordination of ongoing clinical trials at assigned sites.Training & Development- Undergo comprehensive training in monitoring processes and Good Clinical Practice (GCP).Monitoring Activities- Schedule and conduct monitoring visits to clinical trial sites in...

Job Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical...

We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to...

Job Summary:The Senior Manager of Clinical Research will lead and manage clinical trials and research studies, ensuring that they are completed on time, within budget, and in compliance with regulatory standards. The manager will supervise research teams, collaborate with cross-functional departments, and provide strategic direction for clinical research...

Company DescriptionNovaspire Biosciences Private Limited is a healthcare company specializing in Pharmacovigilance, Clinical Research, and Bioavailability/Bioequivalence studies Project Management support. Novaspire is dedicated to enhancing patient safety and promoting public health through innovative solutions for the pharmaceutical and biotechnology...

Job OpportunityWe are seeking a highly skilled Clinical Research Monitor to join our team.The selected candidate will be responsible for the coordination of ongoing clinical trials at assigned sites, ensuring timely and accurate completion of tasks.Key Responsibilities:Schedule and conduct monitoring visits to clinical trial sites in accordance with study...

Job DescriptionOpen for Delhi and Bangalore location only- Proficient in developing high-quality key clinical trial documents, including protocols, Investigator&aposs Brochures (IBs)- Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).- Proficient in translating complex scientific data into clear, regulatory compliant...

Open for Delhi and Bangalore location only Proficient in developing high-quality key clinical trial documents, including protocols, Investigator's Brochures (IBs) Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs). Proficient in translating complex scientific data into clear, regulatory compliant documents that...

Job Title: Clinical Research Coordinator II", "About the Role:", "We are seeking a highly motivated and organized individual to fill the position of Clinical Research Coordinator II. The successful candidate will be responsible for coordinating clinical trial activities, including participant recruitment, informed consent, and sample collection.", "Key...

About the RoleAs a key member of our team, you will be responsible for managing participant interactions and sample collections. Your primary focus will be on ensuring the success of clinical trials through effective recruitment, informed consent processes, and regular follow-ups."> Develop and implement strategies for participant recruitment, adhering to...