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...

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...

**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 Research, Good at Searching, Reading between the lines, compiling data from various sources and repeating it, umpteen number of times daily. **Here is your...

Fusion Market Research is hiring for Research Associate **Responsibilities** Key responsibilities: 1. Conduct Secondary / Primary research 2. Create Market Research report 3. Product research using search engine 4. Work on company profiling, SWOT analysis, Report writing, Article writing 5. Project delivery in market research, 6. Generate quantitative...

Fusion Market Research is hiring for Research Associate/ Research Analyst **Responsibilities** Key responsibilities: 1. Conduct Secondary / Primary research 2. Create Market Research report 3. Product research using search engine 4. Work on company profiling, SWOT analysis, Report writing, Article writing 5. Project delivery in market research, 6....

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...

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...

Your responsibilities include, but are not limited to: - Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial. Recommends sites to participate in clinical trial - Is the frontline liaison between Statistical and sites to ensure successful collaboration, meeting Statistical expectation on milestone and...

Fusion Market Research is hiring for Research Associate **Key responsibilities**: 1. Conduct Secondary / Primary research 2. Create Market Research report 3. Product research using search engine 4. Work on company profiling, SWOT analysis, Report writing, Article writing 5. Project delivery in market research, 6. Generate quantitative and qualitative...

Fusion Market Research is hiring for Market Research **Responsibilities** Key responsibilities: 1. Conduct Secondary / Primary research 2. Create Market Research report 3. Product research using search engine 4. Work on company profiling, SWOT analysis, Report writing, Article writing 5. Project delivery in market research, 6. Generate quantitative...

Designation: Onco-Psychologist (Clinical Psychology) Education Qualification: MSc Clinical Psychology / M.Phil Experience: 2-5 years in cancer patient counseling and associated research. Job Purpose: To be an integral part of the Clinical and Research team, focusing on meeting the psychosocial needs of breast cancer patients and their families, while...

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...

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...

develop and write trial protocols (outlining purpose and methodology) - present trial protocols to a steering committee - design data collection forms, known as case report forms (CRFs) - identify and assess the suitability of facilities to use as the clinical trial site - identify/select an investigator who will be responsible for conducting the trial at...

develop and write trial protocols (outlining purpose and methodology) - present trial protocols to a steering committee - design data collection forms, known as case report forms (CRFs) - identify and assess the suitability of facilities to use as the clinical trial site - identify/select an investigator who will be responsible for conducting the trial at...

**About Infogence**: Infogence is a leading global market research firm. We provide off-the-shelf reports with robust industry coverage and a focus on new and emerging technologies. Our market research reports have helped several startups to Fortune 500 companies make informed and effective decisions. We cover a wide range of industries and offer actionable...