Clinical Research Associate

**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**: -...

We are seeking an enthusiastic and detail-oriented Clinical Research Associate to join our team. This entry-level position is ideal for recent graduates looking to launch their career in clinical research. As a Clinical Research Associate, you will play a critical role in the development, implementation, and monitoring of clinical trials, ensuring compliance...

_**Responsibilities for Clinical Research Associate **_ - Recruit and enroll study participants - Input clinical research data into electronic data systems - Coordinate patient visits and procedures related to research - Act as resource for study participants by answering questions and explaining related procedures - Ensure the study site is compliance with...

We are seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) to join our team. This entry-level position is ideal for recent graduates or individuals with mínimal experience in clinical research who are looking to start their careers in this dynamic field. As a CRA, you will be responsible for overseeing and monitoring clinical...

Experience in Clinical research. Must have well experienced in Clinical research coordinator clinical data management - 5- 8 years Pay: ₹10,000.00 - ₹15,000.00 per month Schedule: - Day shift - Morning shift Supplemental pay types: - Shift allowance **Education**: - Bachelor's (preferred) **Experience**: - Teaching: 1 year (preferred) - Making...

Clinical Research Associate (Interns / Freshers) **Pre-Trial**: - Identify and qualify potential clinical trial sites and investigators. - Set up and equip trial sites with the necessary materials and equipment. - Train site staff on study procedures and data collection methods. - Develop and maintain study manuals and documentation. **Monitoring**: -...

all Clinical Research Topic: - DRUG DEVELOPMENT: FROM MOLECULE TO PRESCRIPTION: PART 1 DRUG DEVELOPMENT: FROM MOLECULE TO PRESCRIPTION: PART 2 THE EVALUTION OF THE CLINICAL TRIAL PROCESS-A BRIEF HISTORY LESSON HISTORICAL BACKGROUND OF GCPINSTITUTIONAL REVIEW BOARD/INDEPENDENT ETHICS COMMITTEE (IRB/IEC)STAKEHOLDERS ENGAGEMENT TO ENSURE A SUCCESSFUL TRIAL...

As a clinical research associate (CRA), you'll **run clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe for the intended use**. Pay: Up to ₹27,000.00 per month **Benefits**: - Health insurance - Provident Fund Schedule: - Day shift Supplemental Pay: - Yearly bonus Work Location: In person

Ascentrik Research Pvt. Ltd is a premier Research & Data Service Provider serving the Top Fortune 500 Companies & many more Multi-National Companies across different industries & sectors. We are pioneers in customized Research Services and are providing actionable insights with quality data to our clients. We are operating with a large work force from...

Overall, clinical data managers are responsible for collecting data from a variety of medical research projects, such as clinical and pharmaceutical trials. They work collaboratively to make sure data is collected, managed and reported clearly, accurately, and securely. Clinical Research Coordinator Responsibilities: Overseeing the smooth running of...

**Clinical Research Associate (CRA)** Clinical Research Associate also known as monitor is employed by either a pharmaceutical company or a contract research organization (CRO) which works on behalf of pharmaceutical companies. Clinical trials may be carried out at various phases, trials on patients with a disease, and studies conducted after the launch of...

Clinical research studies are conducted by a multidisciplinary research team including but not limited to clinical staff, regulatory staff, and administrative personnel. The coordination among such a comprehensive team is often led by a clinical research coordinator (CRC), whose daily responsibilities vary significantly but ultimately serve as the liaison...

Pacifix Research is seeking a motivated and detail-oriented Clinical Research Coordinator to join our team. This is an excellent opportunity for fresh graduates interested in starting their career in clinical research. The Clinical Research Coordinator will play a crucial role in coordinating and managing clinical trials, ensuring compliance with regulatory...

Job Description Skills: Clinical Research, Clinical, Research, CR, Pharmacovigilance, Regulatory Affairs, Clinical Trials, As a Senior CRA, you will participate in the preparation and execution of Phase I-IV clinical BA/BE studies with a particular focus on monitoring and site management activities to ensure timelines and deliverables are met at assigned...

Hiring for our client companies for multiple vacancies in Clinical Research(CRA,CRC) Clinical Research Assistant **Responsibilities**: - Monitor clinical trials and take notes on activities - Ensure compliance with all clinical trial protocols - Enter clinical research data into appropriate fields - Transfer data from paper formats via computer,...

We are seeking a motivated individual to join our team as a Clinical Research Coordinator. This entry-level position offers an exciting opportunity for individuals interested in launching their career in clinical research. As a Clinical Research Coordinator, you will be responsible for assisting in the coordination and management of clinical trials, ensuring...

**Job description** **Responsibilities**: - Collecting, registering and archiving information and documents in accordance with the applicable GCP guidelines for clinical studies, both for local and international studies; - Prepare ISF (investigator site file) and TMF (trial master file) for the initiation of participating centers in clinical studies; -...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...

Creating and writing trial protocols, and presenting these to the steering committee. - Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial. - Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. - Ordering, tracking, and managing IP...