Clinical Research Physician

Company DescriptionWe suggest you enter details here.Role DescriptionThis is a full-time on-site role for an MD Physician at Kimaya Heart Institute and Research Centre LLP, located in Gujarat, India. The MD Physician will be responsible for diagnosing, treating, and managing patients with a wide range of cardiological conditions. The role involves performing...

The Clinical Trial Physician is responsible for providing medical input within the organization as well as to external partners and performing medical review tasks within the context of clinical trials. Furthermore, the Clinical Trial Physician is responsible for undertaking scientific/medical writing tasks within the organization.Role & responsibilitiesIs...

S3 Clinical Research is expanding, and we are looking for adedicated Phlebotomistto join our team. Position:Phlebotomist Organization:S3 Clinical Research - Clinical Lab Vertical Location:Ahmedabad Joining:ImmediateKey Responsibilities:Collecting and handling blood samples with precision and care.Maintaining proper labeling, documentation, and storage of...

About the Role:Key role as a project manager would be Single Point of Contact (SPOC) for the Sponsor from Sterling Accuris Wellness Pvt. Ltd. for laboratory testing and the associate services for clinical trials.The role will require the ability to support the clinical trial study pipeline which could include various projects covering various therapeutic...

Company DescriptionHREE Research Pvt. Ltd. is a full-service Clinical Research Organization (CRO) offering comprehensive, end-to-end clinical research solutions. We specialize in supporting pharmaceutical, biotechnology, and medical device companies across all phases of clinical trials. Our services include study design and protocol development, regulatory...

*QC Reviewer (Clinic):*1) Review of clinical raw data as per predefined Quality Control Plan for completeness, accuracy, and for compliance with the Study Protocol, GCP, SOPs and applicable regulatory Guidelines.2) Online Monitoring of study activities to ensure that studies are conducted in accordance with GCP, SOPs, Protocol and applicable regulatory...

Overseeing the trouble-free running of clinical trialsCollecting data obtained from research, coding and analyzing itManaging budgets set aside for researchCommunicating with participants regarding study objectivesAdministering questionnaires and monitoring participants to ensure they adhere to the studys rulesLiaising with laboratories regarding research...

Dear Candidate,Below are the Job Details for Clinical SAS Programmer role at CBCC Global Research LLP.Candidate should have the exposure of SDTM, ADAM and TLF.Job Location : Ahmedabad At OfficePosition : 2Experience: 2-5 years in CRO preferred / Pharma industryQualification : M. Sc. Statistics/Any Science GraduateMandatory experience in Clinical...

ResponsibilitiesOversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities.Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study...

Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research – approaching each opportunity with foresight, character, resilience and innovation. Based on decades of...