3.0 - 7.0 years

0 Lacs

karnataka

On-site

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...

Posted 1 week ago

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Clinical Research Associate (CRA) MSD

2.0 - 6.0 years

0 Lacs

haryana

On-site

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...

Posted 1 month ago

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R&D Executive (Ayurvedic Beauty & Personal Care) - Hyderabad Location Skandhanshi Infra Projects

3.0 - 6.0 years

2 - 3 Lacs

hyderabad

Work from Office

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...

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Floor Coordinator NIDAN PRIME (SGLA)

2.0 - 6.0 years

0 Lacs

maharashtra

On-site

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.,

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Clinical Research Associate I IQVIA India

1.0 - 5.0 years

0 Lacs

delhi

On-site

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...

Posted 3 months ago

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