Clinical Trial

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...

**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**: -...

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...

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...

Work as part of solutions and presales team.- - SME in clinical space o Solutions, offerings & PoV building o GTM Strategy and planning.- - Assist business development teams and managing solutioning for RFPs etc.- - Provide necessary domain support to insides sales/marketing teams on campaigns/lead generation activities.- - Keep up with key industry trends &...

**Responsibilities** - Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations - Serve as primary Sponsor contact for operational project-specific issues and study deliverables - Maintain in depth knowledge of protocol, therapeutic...

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 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...

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: -...

Monitoring clinical studies of investigational and approved products that have been determined to satisfy a medical need and/or offer a commercial benefit. This may include the following site visits: qualification, initiation, interim, and close out - Managing and training site personnel on therapeutic area, protocol requirements, proper source...

OVERVIEWAs a global leader in Translations, Life Sciences Consulting, and eTMF, TransPerfect helps life sciencescompanies manage, track, and execute clinical trials. Technical Project Managers provide implementation projectand technical leadership to customer deployments, as well as integrations, migrations/transfers, upgrades,validations, and product...

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...

From 5 to 10 year(s) of experience ₹ Not Disclosed by Recruiter - Pune, Trivandrum/Thiruvananthapuram - Should have minimum 5 Years of experience. - Have experience on Clinical Trials, 6, Good Clinical Practices, Quality Risk Management in Clinical Trials - Literature Monitoring/review - Should have experience in embase database, case processing, quality...

OVERVIEWAs a global leader in Translations, Life Sciences Consulting, and eTMF, TransPerfect helps life sciencescompanies manage, track, and execute clinical trials. Technical Project Managers provide implementation projectand technical leadership to customer deployments, as well as integrations, migrations/transfers, upgrades,validations, and product...

OVERVIEW As a global leader in Translations, Life Sciences Consulting, and eTMF, TransPerfect helps life sciences companies manage, track, and execute clinical trials. Technical Project Managers provide implementation project and technical leadership to customer deployments, as well as integrations, migrations/transfers, upgrades, validations, and product...

OVERVIEWAs a global leader in Translations, Life Sciences Consulting, and eTMF, TransPerfect helps life sciencescompanies manage, track, and execute clinical trials. Technical Project Managers provide implementation projectand technical leadership to customer deployments, as well as integrations, migrations/transfers, upgrades,validations, and product...