Centralized Study Assoc Ii

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...

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. Conducting operations in...

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...

Follow all applicable departmental Standard Operating Procedures and Work Instructions. Complete required trainings according to required timelines. Complete day-to-day tasks ensuring quality and productivity. Manage project and technical documentation in an appropriate manner. Provide administrative and technical support to internal departments and...

Operations Manager II, 3P Central Job DescriptionThe Operations Manager II, 3P Central is a critical role that drives compliance culture through risk and mitigation actions, centrally manages the 3P SC Network Performance by ensuring process improvements and apt review models, and handles commercial negotiations and loss recovery with 3P Partners in...

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...

Job Title: Medical Data Review Specialist IIFortrea Development India Pvt Ltd is seeking a highly skilled Medical Data Review Specialist II to join our team. As a key member of our Global Medical Data Review Team, you will be responsible for executing Central Medical Review activities and assisting senior staff and Medical Monitors in their...

Job Title: Medical Data Review Specialist IIFortrea Development India Pvt Ltd is seeking a highly skilled Medical Data Review Specialist II to join our team. As a senior member of the Global Medical Data Review Team, you will be responsible for executing key Central Medical Review activities and assisting senior staff and Medical Monitors in their...

As a leading global contract research organization (CRO), Fortrea provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.The Medical Data Review Specialist II is a senior member of the Global Medical Data Review Team...

ICON is looking for a Central Monitor to be based in Chennai. The Central Monitor is responsible for listing review and central data analysis to support quality and risk reviews of projects, by highlighting/escalating trends. Job Responsibilities As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement...

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.The Medical Data 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...

Job Summary: We are seeking a skilled Medical Data Review Specialist II to join our Global Medical Data Review Team. The successful candidate will be responsible for the execution of key Central Medical Review activities and will assist senior staff and Medical Monitors in the execution of their responsibilities.Key Responsibilities:Collaborate with the...

Job Title: Centralized MonitoringAbout the Role:We are seeking a highly skilled and experienced Centralized Monitoring professional to join our team at GSK India Global Services Private Limited. As a Centralized Monitoring Specialist, you will be responsible for ensuring the quality and integrity of clinical trial data, while driving process improvements and...

**At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.** **Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

Key ResponsibilitiesAs a Centralized Monitoring Specialist at 14260 GSK India Global Services Private Limited, you will be responsible for embedding the application of Risk-Based Quality Management aligned with study planning, protocols, GSK SOPs, ICH GCP, and regulatory requirements for assigned GSK-sponsored and outsourced studies.You will drive...

Critical Responsibilities:As a Centralized Monitoring Specialist, you will be responsible for ensuring the quality and integrity of clinical trials by implementing Risk-Based Quality Management aligned with study planning, protocols, GSK SOPs, ICH GCP, and regulatory requirements.You will drive discussions with Global Clinical Operations, Data Strategy and...

Study Start Up Associate II - India, Bangalore ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development At ICON, it’s our people that set us apart. Our...

Key ResponsibilitiesEmbed the application of Risk-Based Quality Management aligned with study planning, protocols, GSK SOPs, ICH GCP, and regulatory requirements for assigned GSK-sponsored and outsourced studies.Drive discussions with Global Clinical Operations, Data Strategy, and Management teams for critical-to-quality measures to prevent study...

Key ResponsibilitiesEmbodies Risk Based Quality Management aligned with study planning, protocols, GSK SOPs, ICH GCP, and regulatory requirements for assigned GSK sponsored and outsourced studies, including Central Monitoring and Data Analytics setup and execution.Leads discussions with Global Clinical Operations, Data Strategy and Management, Stats and...