CRA Manager

We’re looking for people who are determined to make life better for people around the world. Purpose: The purpose of the Associate, Monitoring Oversight role is to be an advocate for monitoring oversight who works with the Clinical Design, Delivery & Analytics (CDDA), the Medicines Quality Organization (MQO) and Investigator Engagement (IE) to ensure...

Daily Role: 1. Along with the above roles, meeting with the MS to discuss daily issues, payables, about feedbacks (IP, op, PHC) 2. To mail "Thanks letters"/ telephone to the in patients who gave the feedback after discharge 3. To have the meeting with coordinators regarding the previous day's issues in the wards, any VIPs etc. 4. Responsible to collect...

**Job Overview**: As a Clinical Research Associate (CRA), your primary responsibility is to ensure the smooth and ethical conduct of clinical trials. You will be responsible for monitoring and managing clinical trial sites, ensuring compliance with protocols, regulations, and company procedures. CRAs play a crucial role in safeguarding the rights and...

Job Title : Clinical Research Associate (CRA) Company : MS Clinical Research Pvt Ltd About 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...

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...

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...

Job Overview Assist and manage assigned tasks related to the coordination, planning, and implementation of Patient Recruitment and Retention operational plans on assigned studies. Collaborate with internal teams and external providers to coordinate aspects delivery of tactics associated with the recruitment/retention strategy. Communicate with internal...

Management of projects under direction of a Project Manager / Director as assigned. - Ensure site monitoring responsibility for clinical studies are conducted according to Standard Operating Procedures, ICH Guidelines and GCP. Work Closely with project teams in implementation of best TRR practices & applicable project plans as assigned (Implementation of...

Management of projects under direction of a Project Manager / Director as assigned. Ensure site monitoring responsibility for clinical studies are conducted according to Labcorp Standard Operating Procedures, ICH Guidelines and GCP. Work Closely with project teams in implementation of best TRR practices & applicable project plans as assigned (Implementation...

Ensure electronic lab data contains all protocol specified lab parameters, is in correct format and data populates to the specified fields and patients correctly. Review data discrepancies generated by study specific edit checks for laboratory data and assist in preparation of data clarification forms sent to the site or the central lab. Also, review...

Key Responsibilities ​ Single point of accountability to embed the application of Risk Based Quality Management aligned with the study planning, study protocols, GSK SOPs, ICH GCP and regulatory requirements for assigned GSK sponsored and outsourced studies.; includes the set up and execution of Central Monitoring and Data Analytics tool Drive...

Ensure electronic lab data contains all protocol specified lab parameters, is in correct format and data populates to the specified fields and patients correctly. - Review data discrepancies generated by study specific edit checks for laboratory data and assist in preparation of data clarification forms sent to the site or the central lab. Also, review...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

**Labcorp Drug Development**: As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services...

**Department - Centralised Monitoring Unit (CMU) - Bangalore** **About the department** The Centralised Monitoring Unit (CMU) - Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Medical reviewers) and technical programmers (Functional programmers, statistical monitors). Medical...

Job Location: Kenvue GCC, BangaloreRequired Qualifications:Associate degree or equivalent +1 year of corresponding experienceIn-depth knowledge and understanding of records and information management practices, rules, and regulations.The ability to define problems, collect data, establish facts, and draw valid conclusions.The ability to identify, recommend...

Job Location: Kenvue GCC, BangaloreRequired Qualifications:Associate degree or equivalent +1 year of corresponding experienceIn-depth knowledge and understanding of records and information management practices, rules, and regulations.The ability to define problems, collect data, establish facts, and draw valid conclusions.The ability to identify, recommend...

Job Location: Kenvue GCC, Bangalore Required Qualifications: Associate degree or equivalent +1 year of corresponding experience In-depth knowledge and understanding of records and information management practices, rules, and regulations. The ability to define problems, collect data, establish facts, and draw valid conclusions. The ability to identify,...

Job Location: Kenvue GCC, BangaloreRequired Qualifications:Associate degree or equivalent +1 year of corresponding experienceIn-depth knowledge and understanding of records and information management practices, rules, and regulations.The ability to define problems, collect data, establish facts, and draw valid conclusions.The ability to identify, recommend...

Central Monitor **Category**:Clinical Development**Location**:Bangalore, Karnataka, IN**Department - Centralised Monitoring Unit (CMU) - Bangalore**About the department** - The Centralised Monitoring Unit (CMU) - Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Medical reviewers)...