Clinical Trial

As a Clinical Research Associate, you will be responsible for managing and monitoring clinical trials. You will work closely with investigators to ensure that all aspects of the study are conducted according to protocol and in compliance with regulatory requirements. Your tasks will include preparing and reviewing study documents, ensuring adherence to...

Key Responsibilities:Lead and manage cross-functional clinical trial teams from study start-up to close-out.Develop, implement, and track study timelines, budgets, and operational plans.Ensure trials are conducted in compliance with ICH-GCP, regulatory requirements, and internal SOPs.Oversee the quality and integrity of trial data and ensure timely data...

**Immediate Joiner** **Job Summary**: We are seeking a highly motivated and detail-oriented Clinical Trial Assistant (CTA) - I to join our clinical operations team. The CTA will support the execution of clinical trials by providing administrative and coordination assistance. This is an entry-level position ideal for recent graduates or those with up to 6...

**About the Role**: We are seeking **enthusiastic and detail-oriented fresh graduates** to join our Clinical Trials Office as **Research Data Coordinators**. This is a fantastic opportunity for recent graduates looking to launch their career in **clinical research**, **healthcare data management**, or **medical data analysis**. **Key Responsibilities**: -...

**Clinical Coder II** **-** **(** **22006832** **)** **Description** **Senior Clinical Coder** Come discover what our 25,000+ employees already know: work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career...

**Site Monitoring**:Conducting regular visits to clinical trial sites to ensure study protocols are followed accurately, including patient recruitment, data collection, and informed consent procedures. - **Data Quality Assurance**:Reviewing and verifying clinical trial data for accuracy and completeness, identifying and resolving discrepancies, and...

Assist in the preparation and coordination of clinical trial protocols and associated documents. - Support the monitoring of clinical trials at various stages, including site initiation, maintenance, and close-out. - Ensure that study sites are compliant with Good Clinical Practice (GCP) and regulatory requirements. - Conduct site visits to assess the...

Company DescriptionAt datAIsm, we specialize in delivering process improvement solutions to optimize efficiency and ensure compliance for diverse industries. Our tools, expertise, and methodologies are designed to elevate outcomes in workflows, supplier quality, defect reduction, and clinical data integrity. With experience across sectors such as...

**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

The clinical research assistant is employed by a hospital or medical research center, who is involved in the administration of clinical trials. In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines. The Clinical Research Coordinator is a specialized research professional working with and under...