Clinical Database Coordinator

**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** -...

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...

Receptionist will be the first point of contact for a Clinic. Receptionist’s duties include offering administrative support across the organization. You will welcome patients and greet them who visit the clinic. You will also coordinate front-desk activities, including distributing correspondence and redirecting phone calls. - Greet and welcome patients as...

**Description** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their...

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 -...

**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...

**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**: -...

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...

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...

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...

Uses common programing languages and assists in customizing proprietary databases for housing of data and employees use, to enter data and make on going changes. Assists in creating client reporting templates and customizing proprietary databases to allow for data reporting by agreed upon users. Supports in ensuring reporting system accepts, integrates and...

Interfacing with sponsors - Checking database constraints - Ensure completion of project within allotted deadlines - Preparation of different types of statistical reports - Resolving any ongoing data and operational problems **Role: - **Clinical Data Associate **Required Qualification: - ** M.Pharm, Pharm D, BDS,MBBS, BAMS, BHMS, BUMS, BSc, MSc (Life...

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...

_**Patient Care **_ 1. Daily Clinical rounds of all patients admitted in ICU complex and updating the case file and clinical notes. 2. Performing bed side procedures as informed by treating consultants/HOD - ICU 3. Taking blood samples, sending to labs and obtaining the reports on time 4. Inform to the seniors, if any reports /values/parameters are...

**Job description** **Role & responsibilities** Medical Coordinator To ensure that all the services are provided as per the guidelines and protocols defined by the organization and within the framework of medical ethics To ensure admission and discharge process are as per the pre-defined TAT To ensure the accuracy of discharge summaries To take a daily...

**Job description** **Qualifiaction**: B. Tech / B. E in CS/IT/EE or MCA;with 4-8 years of IT experience & certifications like OCA- DBA/OCP- DBA/MCDBA - Expert in installation, assembling and maintenance of SQL server and related versions. - Responsible for migration,patching and security management functions of SQL versions. - Evaluation of database server...

We are looking for a highly capable, self-motivated and independent Database Administrators based in India. If you are passionate out Oracle database technology as well as cloud computing, this is the ideal role you’ve been waiting for. Our DBA team supports databases which are available both on-premise and on Cloud. In this role, you will be asked to...