Clinical Trial

Clinical Data Management Job DescriptionWe are looking for a detail-oriented and organized Clinical Data Manager (CDM) to join our expanding clinical research team. The ideal candidate will be a passionate advocate for data accuracy and integrity, ensuring the smooth and efficient flow of clinical trial data from collection to analysis. You will play a...

Clinical Data Management Job Description We are looking for a detail-oriented and organized Clinical Data Manager (CDM) to join our expanding clinical research team. The ideal candidate will be a passionate advocate for data accuracy and integrity, ensuring the smooth and efficient flow of clinical trial data from collection to analysis. You will play a...

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 &...

As a **Clinical SAS Programmer **you will Ssupport all programming activities which will required for the data analysis of the clinical trials and create standard datasets (SDTM) and analysis datasets (ADaM) and generate reports of the form Tables, Graphs and Listings as applicable. - Planning and working with the clinical programming group to schedule...

About the role: The Clinical Operations group is responsible for site management, monitoring tasks and support of clinical trials. The group allocates resources to projects as appropriate to assist with the implementation of project plans and to ensure compliance with regulatory requirements and Standard Operating Procedures. Key Accountabilities: ...

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...

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...

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...

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...

The project manager has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The project manager oversees and coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating...

Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where...