clinical study coordinator

Detail-oriented Clinical Research Coordinator (CRC) with 3+ years of experience supporting Phase I-IV clinical trials across Oncology, Cardiovascular, Infectious Disease, and Pharmaceutical therapeutic areas. Proficient in ICH-GCP E6(R2/R3) guidelines, IRB submissions, eConsent, and regulatory document management. Skilled in Decentralized Clinical Trials...

Role Overview An entry-level Clinical Research Associate (CRA) to monitor clinical trial sites, verify data quality and ensure GCP compliance and patient safety across assigned studies. Key Responsibilities ■ Support and conduct site visits for study initiation, monitoring and close-out ■ Verify source documents against Case Report Forms (CRFs) for...

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Clinical Study Manager (AI Training) About The Role What if your clinical trial expertise could directly shape how AI understands and communicates the science of medicine? We're looking for experienced Clinical Study Managers to support the operational execution of clinical research projects — ensuring studies run on time, within budget, and to the...

Job Tittle - Clinical Study Budget SupportLocation - HyderabadAbout the job:Join the Clinical Study Support and Operations (CSSO) team, where you will play a vital role in supporting clinical study operations while ensuring compliance with global standards and regulations. In support of the Clinical Supply Chain Operations (CSCO) team, who is responsible for...

Clinical Study Manager (AI Training) About The Role What if your clinical trial management expertise could directly shape how AI understands and advances healthcare research? We're looking for experienced Clinical Study Managers to oversee the operational execution of clinical trials — ensuring studies run on time, on budget, and to the highest quality...

Clinical Study Manager (AI Training) About The Role What if your clinical trial management expertise could directly shape how AI understands and reasons about real-world healthcare research? We're looking for experienced Clinical Study Managers to oversee the operational execution of clinical trials — and help ensure the AI systems being trained on this...

We’re looking for a highly organized and self-driven Clinical Research Coordinator (CRC) to support clinical trial execution across partner hospitals centres. In this role, you will be responsible for end-to-end sample and patient data management, ensuring all site-level trial activities are conducted in alignment with study protocols, regulatory...

Job description Role & responsibilities To take care of emergency medical management To ensure Volunteer well-being To ensure proper co-ordination and conduct of the bio study To ensure proper functioning and maintenance of instruments To monitor documentation / records and storage To review employee health check-up reports and promote preventive healthcare...

JOB DESCRIPTION BASIC INFORMATIONPosition Title & DesignationCoordinatorJD CodeSHB/XXX/DEPT/NNNJob FamilyClinicalDepartmentClinical ResearchROLE DETAILSTo be filled up as per the requirement of the Division / unit / function / territoryGradeB1Reporting ToUnit Head DivisionCorporateUnit LOCATION DETAILSPlease mention the correct office location of the Role...

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...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

Clinical Study Manager IIAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part of our global team,...

Clinical Data Coordinator- SeniorAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

DescriptionAt Quanticate, we're pioneers in providing top-tier statistical and data management support to our clients.Are you passionate about clinical research and data excellence? Do you thrive in fast-paced, dynamic environments where your attention to detail can make a real impact on patient outcomes? We’re looking for a Clinical Data Coordinator II to...

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...

We are hiring for Clinical Data Coordinator with minimum 3 years of experience in Clinical data management.About Veramed:Veramed is a biometrics-focused CRO, primarily specializing in Statistics and Statistical Programming. Recently, we have also started expanding into Data Management and are in the process of building dedicated data management teams across...

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...