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**: -...

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.Key Responsibilities:Conduct site visits to monitor trial activities and ensure compliance...

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.Key Responsibilities:Conduct site visits to monitor trial activities and ensure compliance...

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research. Key Responsibilities : Conduct site visits to monitor trial activities and ensure compliance...

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...

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...

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...

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...

A Clinical Research Coordinator is responsible for a variety of duties including the following: - Overseeing the trouble-free running of clinical trials - Collecting data obtained from research, coding and analyzing it - Managing budgets set aside for research - Communicating with participants regarding study objectives - Administering questionnaires and...

We are looking for a motivated and detail-oriented individual to join our team as an Entry-Level Clinical Research Coordinator. This position offers an exciting opportunity for someone passionate about clinical research to gain hands-on experience in coordinating and supporting clinical trials. **Roles and Responsibilities**: - Assist in the coordination...

**Summary**: Monitors patient data & study-related information related to clinical study sites and clinical trial participation.. Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into data validation plan. Provides timely and accurate monitoring of patient data and study-related...

Overseeing the smooth running of clinical trials. - collecting, coding and analyzing data obtained from research. - administrating questionnaires. - associate degree in nursing or related field. - attention to detail. **Salary**: ₹18,000.00 - ₹30,000.00 per month **Benefits**: - Provident Fund Schedule: - Day shift Supplemental pay types: -...

Being Analytical, Excellent in Research, Good at Searching, Reading between the lines, compiling data from various sources and repeating it umpteen times daily.**Research Associate - Data Business - B0223 (FRESHERS ONLY)** **Are you the one?** Sherlock Holmes is a no-brainer! We all have lived the fantasies of becoming one. Being Analytical, Excellent in...

To conduct online offline lectures Drafting of Mock projects Visit to various companies to understand the projects and replicate those in tutorial format for students Conduct offline Sunday classes **Salary**: ₹20,000.00 - ₹40,000.00 per month **Benefits**: - Internet reimbursement Schedule: - Monday to Friday Ability to commute/relocate: -...

393172BR **Clinical Research Medical Advisor**: India **About the role** Novartis is a pioneer in drug development with a robust pipeline across therapy areas. CRMAs work closely with Investigators and ensure scientific engagement with the Investigator community to drive our programs and trials across the globe. Your responsibilities include, but are not...

**Responsibilities**: - Schedule, Plan and Conduct Site Visits: Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits and Site Close-out Visits. - Write Reports and Investigator Follow-up Letters for Site Visits: Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits and Site Close-out Visits. - Compliances: Follow...

As a Market Research Associate, you will play a pivotal role in driving strategic business decisions through comprehensive market analysis and insightful data interpretation. This role demands a passion for research, an analytical mindset, and a keen understanding of market trends. Key Responsibilities: - Conduct in-depth research on companies, industries,...

The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk Indicators, working collaboratively across departments to produce...

Qualification: B. Pham/M. Pharm + diploma in clinical research Location: Pune Experience: 10+ Years