15 Protocol Adherence Jobs

Company Description ZENOVEL is a global leader in the pharmaceutical industry, specializing in providing comprehensive solutions for Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Regulatory Affairs. Our experienced team has over 17 years of expertise in GCP, GMP, and regulatory affairs, and we are dedicated to helping organizations in the pharmaceutical industry achieve success. Role Description This is a full-time on-site role for a Senior Clinical Research Associate at our Ahmedabad location. The Senior Clinical Research Associate will be responsible for Monitoring BA-BE (Healthy Volunteer), overseeing clinical operations, and ensuring protocol compliance. They will ...

Lead the clinical management of critically ill patients and ensure high-quality critical care delivery. Perform essential critical care procedures, including intubation, central line insertion, and other life-saving interventions. Coordinate with ICU staff to plan and execute patient treatment strategies effectively. Monitor adherence to clinical protocols and ensure optimal patient safety standards. Collaborate with multidisciplinary teams to support comprehensive patient care within the ICU. Participate in clinical decision-making, emergency management, and continuous quality improvement activities. Contribute to maintaining accurate clinical documentation and communicating updates to pati...

Lead the clinical management of critically ill patients and ensure high-quality critical care delivery. Perform essential critical care procedures, including intubation, central line insertion, and other life-saving interventions. Coordinate with ICU staff to plan and execute patient treatment strategies effectively. Monitor adherence to clinical protocols and ensure optimal patient safety standards. Collaborate with multidisciplinary teams to support comprehensive patient care within the ICU. Participate in clinical decision-making, emergency management, and continuous quality improvement activities. Contribute to maintaining accurate clinical documentation and communicating updates to pati...

Lead the clinical management of critically ill patients and ensure high-quality critical care delivery. Perform essential critical care procedures, including intubation, central line insertion, and other life-saving interventions. Coordinate with ICU staff to plan and execute patient treatment strategies effectively. Monitor adherence to clinical protocols and ensure optimal patient safety standards. Collaborate with multidisciplinary teams to support comprehensive patient care within the ICU. Participate in clinical decision-making, emergency management, and continuous quality improvement activities. Contribute to maintaining accurate clinical documentation and communicating updates to pati...

Lead the clinical management of critically ill patients and ensure high-quality critical care delivery. Perform essential critical care procedures, including intubation, central line insertion, and other life-saving interventions. Coordinate with ICU staff to plan and execute patient treatment strategies effectively. Monitor adherence to clinical protocols and ensure optimal patient safety standards. Collaborate with multidisciplinary teams to support comprehensive patient care within the ICU. Participate in clinical decision-making, emergency management, and continuous quality improvement activities. Contribute to maintaining accurate clinical documentation and communicating updates to pati...

Lead the clinical management of critically ill patients and ensure high-quality critical care delivery. Perform essential critical care procedures, including intubation, central line insertion, and other life-saving interventions. Coordinate with ICU staff to plan and execute patient treatment strategies effectively. Monitor adherence to clinical protocols and ensure optimal patient safety standards. Collaborate with multidisciplinary teams to support comprehensive patient care within the ICU. Participate in clinical decision-making, emergency management, and continuous quality improvement activities. Contribute to maintaining accurate clinical documentation and communicating updates to pati...

Lead the clinical management of critically ill patients and ensure high-quality critical care delivery. Perform essential critical care procedures, including intubation, central line insertion, and other life-saving interventions. Coordinate with ICU staff to plan and execute patient treatment strategies effectively. Monitor adherence to clinical protocols and ensure optimal patient safety standards. Collaborate with multidisciplinary teams to support comprehensive patient care within the ICU. Participate in clinical decision-making, emergency management, and continuous quality improvement activities. Contribute to maintaining accurate clinical documentation and communicating updates to pati...

As a Junior Clinical Research Associate at Clinogenesis Research Organization, you will play a crucial role in supporting the clinical operations team and contributing to high-quality clinical trials. **Key Responsibilities:** - Assist in site initiation, monitoring & close-out activities - Support review of study documents & source data verification - Maintain trial documentation & ensure GCP compliance - Coordinate with site teams & internal stakeholders - Assist in reporting, study tracking & CAPA follow-ups - Ensure patient safety and protocol adherence **Qualifications:** - Bachelors/Masters in Life Sciences / Pharmacy / Nursing / Biotechnology - 01 year of experience - Understanding of...

As a healthcare facility manager, you will be responsible for overseeing daily operations to ensure a smooth patient flow, manage staff effectively, and maintain a clean and organized environment. Your role also involves ensuring compliance with protocols and standards to meet regulatory requirements. Key Responsibilities: - Oversee daily operations of the healthcare facility - Ensure smooth patient flow and timely services - Manage and coordinate staff schedules and duties - Maintain a clean and organized environment in the facility - Ensure compliance with protocols and standards set by regulatory bodies Qualifications Required: - Bachelor's degree in healthcare administration or related f...

You will be responsible for the following tasks in this role: - Prepare quantity sheet based on onsite data and drawings - Create Bill of Quantities (BOQ) and bills using item rates - Generate and process subcontractor bills - Coordinate with the site team to take measurements - Ensure that work is completed according to the company's protocols - Verify measurements and bills accuracy Qualifications required: - Proven experience in quantity surveying or related field - Proficiency in using relevant software for quantity estimation - Strong attention to detail and accuracy in calculations You will also enjoy the following benefits: - Cell phone reimbursement - Health insurance - Provident Fun...

As a member of the project team at Fortrea, you will be responsible for conducting clinical data review, query generation/resolution, and reconciliation activities to ensure the delivery of clinical data meets client quality and integrity specifications, project timelines, and productivity targets. Your tasks will include assisting in developing the project Data Management Plan, executing data review guidelines/edit check, and eCRF specification, and contributing to the setup of data management systems based on project requirements. Your key responsibilities will involve: - Ensuring strict adherence to relevant protocols, global harmonized SOPs, and GCP standards for allocated projects. - Fo...

Role Overview: As a Clinical Research Associate (CRA), you will be responsible for performance and compliance for assigned protocols and sites in a specific country. Under the guidance of the CRA-Manager, you will ensure the adherence of study conduct to ICH/GCP and country regulations, company policies and procedures, quality standards, and reporting requirements for adverse events internally and externally. Your primary role will involve acting as the main point of contact and site manager throughout all stages of a clinical research study, assuming overall responsibility for allocated sites. You will actively contribute to the development and expansion of the territory for clinical resear...

Role & responsibilities Formulation Development: Develop and optimize Ayurvedic beauty and personal care products (skin, hair, bath, body, etc.). Conduct ingredient research, compatibility studies, and stability trials. Incorporate clean, Ayurvedic, and natural actives aligned with brand philosophy. Regulatory & Compliance: Ensure all products meet AYUSH and GMP guidelines. Prepare documentation for license applications , label approvals, and regulatory submissions. Stay updated with changes in cosmetic and Ayurvedic product regulations. Quality & Protocol Adherence: Establish and monitor strict lab protocols , batch records, SOPs, and hygiene standards. Oversee Quality Control (QC) procedur...

As a full-time employee, you will be responsible for overseeing the daily operations in a healthcare setting. Your main duties will include ensuring smooth patient flow, managing staff effectively, and maintaining a clean and organized environment. It is crucial to uphold compliance with protocols and standards to ensure the quality of care provided to patients. The work schedule for this position is on a day shift basis, and the work location is in person.,

As a Clinical Research Associate -I, your role will involve performing monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations, guidelines, and sponsor requirements. Your essential functions will include conducting site monitoring visits, working with sites to drive subject recruitment plans, administering protocol and study training to sites, and evaluating the quality and integrity of study site practices. You will also be responsible for managing the progress of assigned studies, maintaining documentation regarding site management, collaborating with study team members, and su...