7 Gcp Principles Jobs

As a Contracts Specialist at Fortrea, your role involves preparing, negotiating, and assisting in the execution and retention of site agreements, confidentiality agreements, and other contracts for Sponsors contracting Fortrea's services. You will be responsible for maintaining contracts tracking and status systems, ensuring compliance with SOPs, and completing study-related duties according to relevant process documents. Your primary focus during site maintenance activities will be collecting investigator and essential documents for studies, ensuring timely applications to regulatory authorities, and meeting documentation requirements. Key Responsibilities: - Adherence to standard operating...

As a Clinical Research Associate at Sun Pharma Laboratories Ltd in Bhubaneshwar, your primary responsibilities will include: - Performing site feasibility, identifying potential investigators, negotiating study budgets, finalizing investigators and sites, and executing CDA and study-related contracts - Preparing and submitting study documents for EC permission across various centers - Overseeing and documenting IP dispensing, inventory management, and reconciliation - Ensuring timely site initiation, monitoring, and close-out activities, along with generating necessary reports - Providing training to investigators and site personnel on study protocols, procedures, and GCP principles - Facili...

Clinical Trial Coordinator (CTC) Location: [Insert City / Across India Hybrid / On-site] Organization: Clinogenesis Research Organization Department: Clinical Operations Employment Type: Full-Time About Clinogenesis Clinogenesis Research Organization is a rapidly growing, innovation-focused CRO dedicated to advancing high-quality clinical research and data-driven healthcare solutions. We are committed to training and developing fresh talent, offering a strong foundation for those aspiring to build a successful career in the clinical research industry. About the Role We are seeking an enthusiastic and detail-oriented Clinical Trial Coordinator (CTC) to support our clinical operations team in ...

As an Associate Medical Reviewer at Novo Nordisk Global Business Solutions (GBS) India, located in the Centralised Monitoring Unit (CMU) department in Bangalore, Karnataka, IN, you will have the opportunity to work in a challenging and dynamic environment. Your primary role will involve conducting comprehensive medical reviews of clinical trial data across various therapy areas within the drug development portfolio. Your key responsibilities will include: - Ensuring the highest quality and consistency of medical data - Emphasizing patient safety, protocol adherence, and compliance with GCP, ICH guidelines, local regulations, and SOPs - Collaborating closely with study team members such as Da...

As a Clinical Research Associate at Sun Pharma Laboratories Ltd in Bhubaneshwar, your responsibilities will include conducting site feasibility assessments, identifying potential investigators, negotiating study budgets, finalizing investigators and sites, and executing study-related contracts. You will be responsible for preparing and submitting study documents for EC permission, overseeing IP dispensing, managing inventory, and ensuring reconciliation. Additionally, you will play a key role in ensuring timely site initiation, monitoring, and close-out activities, as well as conducting investigator and site personnel training on study protocols, procedures, and GCP principles. Your tasks wi...

As a Clinical Research Associate based in Bhubaneshwar, your primary responsibilities will include performing site feasibility assessments, identifying potential investigators, negotiating study budgets, finalizing investigators and sites, and executing CDA and study-related contracts. You will also be responsible for preparing and submitting study documents for EC permission across centers, overseeing IP dispensing, managing inventory, and conducting reconciliations. In addition, you will play a key role in ensuring timely site initiation, monitoring, and close-out activities, as well as overseeing investigator and site personnel training on study protocols, procedures, and GCP principles. ...

The Associate Medical Reviewer position at Novo Nordisk Global Business Solutions (GBS) India, specifically in the Centralised Monitoring Unit (CMU) department in Bangalore, Karnataka, IN, offers a challenging and dynamic environment for individuals who are motivated by working closely with key stakeholders and strive for continuous improvement in their career objectives. As an Associate Medical Reviewer, you will play a crucial role in conducting comprehensive medical reviews of clinical trial data across various therapy areas within the drug development portfolio. Your responsibilities will include ensuring the highest quality and consistency of medical data, with a strong emphasis on pati...