Jobs: clinical investigator

Quantys Clinical Pvt. Ltd. (Rusan Pharma) is Hiring for Clinical Investigator Having Experience of Minimum 01 Year - 04 Year at Gandhidham Location. Department - Clinical Designation - Clinical Investigator Qualification - M.B.B.S. Job Profile - Compiling the medical examination of volunteers with clinical investigations lab reports for certifying the...

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...

Leads Clinical Research and Bio Services Pvt. Ltd is hiring Clinical Research Coordinators in Chennai and Bangalore. Experience: 1 year months to 5 years Qualification: Degree with Life Science background, Diploma in Clinical Research, MSc. Clinical Research, Pharm D Core Responsibilities - Coordinate Screening and Consenting process, Source...

Site selection and qualification - Meet with Clinical Investigators and staff prior to study initiation to ensure all aspects of the study are understood by the investigator and staff, if required train the study site team - Ensures dossier submission at sites, approval and site initiation visit - Ensuring targeted recruitment - Monitor study progress to...

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,...

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,...

1. Having an insight regarding the study materials shared and presenting the same to the concerned doctor 2. Completing the documents like Feasibility Questionnaire, Confidentiality Disclosure Agreement, Investigator Undertaking etc.. required for study Start-Up activity. 3.Collection of documents like calibration certificates, lab documents etc.. from the...

1. Having an insight regarding the study materials shared and presenting the same to the concerned doctor 2. Completing the documents like Feasibility Questionnaire, Confidentiality Disclosure Agreement, Investigator Undertaking etc.. required for study Start-Up activity. 3.Collection of documents like calibration certificates, lab documents etc.. from the...

1. Having an insight regarding the study materials shared and presenting the same to the concerned doctor 2. Completing the documents like Feasibility Questionnaire, Confidentiality Disclosure Agreement, Investigator Undertaking etc.. required for study Start-Up activity. 3.Collection of documents like calibration certificates, lab documents etc.. from the...

1. Having an insight regarding the study materials shared and presenting the same to the concerned doctor 2. Completing the documents like Feasibility Questionnaire, Confidentiality Disclosure Agreement, Investigator Undertaking etc.. required for study Start-Up activity. 3.Collection of documents like calibration certificates, lab documents etc.. from the...

1. Having an insight regarding the study materials shared and presenting the same to the concerned doctor 2. Completing the documents like Feasibility Questionnaire, Confidentiality Disclosure Agreement, Investigator Undertaking etc.. required for study Start-Up activity. 3.Collection of documents like calibration certificates, lab documents etc.. from the...

1. Having an insight regarding the study materials shared and presenting the same to the concerned doctor 2. Completing the documents like Feasibility Questionnaire, Confidentiality Disclosure Agreement, Investigator Undertaking etc.. required for study Start-Up activity. 3.Collection of documents like calibration certificates, lab documents etc.. from the...

Hyderabad 02 to 06 Years Full Time - Plan and conduct investigator site selection audits and clinical trial study audits at investigator sites in accordance with applicable GCP guidelines and regulations. - Review of CRF design - Review of standard operating procedures - Issue audit reports to the investigator site staff and other concerned study personnel -...

**Clinical Research Associate (CRA)** Clinical Research Associate also known as monitor is employed by either a pharmaceutical company or a contract research organization (CRO) which works on behalf of pharmaceutical companies. Clinical trials may be carried out at various phases, trials on patients with a disease, and studies conducted after the launch of...

**About the position** The Clinical Research Associate is responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete and verifiable from source documents. **Core Responsibilities** Monitoring of investigational sites as per ICH GCP 5.18 (Monitoring) and the Clinical Monitoring...

Clinical Project ManagerLocation – Hyderabad #LI HybridAbout the Role:This role is responsible to Lead and manage a multidisciplinary cross functional Clinical Trial Team (CTT) (medical writing, statistics, data management, monitoring partner, drug supply, regulatory, safety etc.) or support the Sr. CPM (where applicable) in the effective planning, regular...

Job Purpose: Working independently and reliably showing a high level of ownership, with a strong focus on detail and committed to the Collection, qualitative data entry, validation, and analysis of the Project related data and analyzes operational information of various sources including the Contracts related to the Investigators. Assist the Project leader...

Job Purpose: Working independently and reliably showing a high level of ownership, with a strong focus on detail and committed to the Collection, qualitative data entry, validation, and analysis of the Project related data and analyzes operational information of various sources including the Contracts related to the Investigators. Assist the Project leader...

Key Responsibilities:Job Title: Clinical Research Associate / Sr Clinical Research AssociateStrategy/Planning, execution, and monitoring of clinical trial,Overview:As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites,...

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...