Clinical Research Coordinator

**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...

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 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...

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...

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...

**Job Summary** - Clinical data curation into a database. - Data management, analysis and interpretation. - Managing Clinical Data administrative operations. - Writing of project reports. - Will get to attend one national conference in a year, based on the performance. **Responsibilities and Duties** **Required Experience, Skills and Qualifications** -...

**Responsiblities**: - Provide clinical study start up expertise. - Assist Lead CRA in the preparation of IRB submissions including the review of the sitespecific informed consent and assent forms - Track IRB submissions - Collect, review, and process essential documents and identify issues that site needs to address. - Communicate to site the updates...

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...

Will be required to coordinate and assist in clinical trial functions Data management pertinent to the clinical trial Assist in patient recruitment Perform basic diagnostic tests such as ECG, Lung function tests, etc Facilitate other diagnostic tests Must be efficient in team work **Job Types**: Full-time, Contract **Salary**: ₹12,000.00 -...

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...

**Job description** **Job Requirements and Responsibilities** - PhD in Life sciences with 4+ years of postdoctoral experience and has a strong molecular biology or cancer biology background. PhD and Post-Doc from a reputed national or international institution. - Position will require to design, initiate and lead various breast cancer clinical and/or...

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...

Create content pieces that appeal to our audiences, attract customers and boost our brand awareness. - Produce content marketing campaigns to drive leads and subscribers. - Utilize SEO best practices to generate traffic to our website. - Oversee our website, promote our blog and pitch articles to third-party platforms effectively. - Work together with...

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...

C. Essential Job Duties:  The below statements are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties.  Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of...

Overview "Primary responsibilities will include supporting the research team in a wide capacity of tasks. Responsible for various reporting on a monthly, quarterly and yearly basis. Creates and maintains various databases on a weekly/monthly/quarterly basis for the research team. Edits presentations for internal and external meetings. Updates database of...

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...