Clinical Research Coordinator

Eligibility: - Graduate / Post Graduates in Life Sciences/ Pharmacy from a reputed institute - Prior knowledge of the conduct of Clinical Trials, - Phases of Clinical trials and - Thorough Knowledge of ICH-GCP and other regulatory guidelines. Roles and Responsibilities: - Prepare the Database of the Investigators at the place assigned to you. - Interact...

We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to...

**Title**: Clinical Programmer **Department**: Engineering Support the organization’s mission, vision, and values by exhibiting the following behaviors: excellence and competence, collaboration, innovation, respect, commitment to our community, and accountability and ownership. Job SummaryPrimary responsibilities are clinical programming and data...

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 Purpose/Summary: Responsible for the management of clinical imaging data (e.g. PET, SPECT, CT, MRI) for clinical research trials, including; receipt, review, reconciliation, and transfer of data coming from research centers worldwide. Also responsible for general project coordination including data entry and tracking. This position is critical to...

The primary responsibility of the Clinical Coordinator is to ensure smooth flow of all the clinical operations. - Responsible for smooth running of the unit and patient experience. - Ensures work is performed in accordance with internal SOPs and working practices, and other regulations. Coordinate with all doctors in the clinic - Effectively communicate...

Job Summary: We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical trial processes, regulatory...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...

ResponsibilitiesSupport CRAs with the setup monitoring and closeout of clinicaltrials in accordance with Good Clinical Practice (GCP) ICHguidelines and company SOPs. Assist in sitequalification initiation and monitoringvisits. Review and track clinical trialdocumentation ensuring accuracy andcompleteness.Collaborate with crossfunctionalteams to address...

Apply for Clinical Research Associate, Career Progress Consultants in Hyderabad/ Secunderabad for 0 - 3 Year of Experience on

Apply for Clinical Research Associate, Career Progress Consultants in Hyderabad/ Secunderabad for 0 - 3 Year of Experience on TimesJobs.com.

Clinical Coordinator is a full time job available immediately (work from home). **Location**: All work will be from home via phone and computer. All initial and ongoing training will be provided. Most of tasks will be very basic including supervision of other staff and answering patients basic questions and daily reporting to leadership. **Job...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP...

Your responsibilities include, but are not limited to:May lead studies in maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development of...

Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by diversity and inclusion,...

JOB DETAILS 1. Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions2. Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with...

“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program, across all disease areas. Be part of a dedicated, passionate team that is diligently providing clinical and scientific inputs at study and...

Job summary At Amazon we believe that every day is still day one and we are working to be the Earth’s Best Employer. To get there, we need exceptionally talented, bright, and driven people. If you’d like to be a part of Disability Leave Services (DLS) Clinical team to provide your clinical expertise for leave of absence, disability and accommodation...

**Summary**: Ensure compliance with internal and external guidelines, to compile and add electronic navigation to clinical and regulatory documents. Support the timely submission of documents to the Health Authorities (HAs) and provide publishing consultancy to the clinical teams and other line functions. **About the Role**: **Major accountabilities**: -...