Clinical Coordinator

As part of a study team, participates in processing and quality assurance checks of clinical trial data to ensure data integrity and consistency. Has direct contact with the trial sponsors and internal and external team members. Performs established processing techniques across multiple imaging modalities using proprietary and third-party package software.

Position Title: Clinical Coordinator - FemaleDepartment: Clinical OperationsLocation: Banjara Hills, HyderabadReports To: Centre ManagerQualifications & Skills RequiredEducation: BDS (Bachelor of Dental Surgery) / BAMS (Bachelor of Ayurvedic Medicine & Surgery) – preference for healthcare background.Experience: 1–3 years in clinical coordination,...

About Our Clinical Trial OpportunityOur organization is seeking a seasoned Clinical Research Coordinator to spearhead clinical trial activities at our site. As a critical member of our team, you will ensure seamless execution of study protocols and compliance with regulatory requirements.Key Responsibilities:Coordinate and manage day-to-day clinical trial...

Company Description **MakroCare |** **_A MakroGroup Company_**MakroCare is an Expert Strategic Development and Commercialization Global Partner for the Pharmaceutical, Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a New Dimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research,...

Job Title:Clinical Trials CoordinatorWe are seeking a skilled professional to support the management of clinical trials. As a key member of our team, you will be responsible for ensuring compliance with regulatory requirements and coordinating submissions in various systems.Main Responsibilities:Assignments: Be assigned to one or more projects under...

Job Title: CSAR ManagerAre you a detail-oriented and analytical professional seeking a challenging role in the life sciences industry? We are looking for a skilled CSAR Manager to join our team. In this position, you will be responsible for providing technical support to clinical study teams, coordinating programming efforts, and ensuring timely delivery of...

Job description Support a PI sponsored Investigational New Drug (IND) or Investigational Device Exemption (IDE) Host/ prepare for external audits (sponsor, FDA, NIH, etc) Monitor or audit studies in the institution Facilitate and/or run research/project team meetings Prepare study budget Educate and mentor clinical staff, research team and other...

Job DescriptionJob SummaryThis position is responsible for configuring, managing, and supporting clinical research teams in data entry and validation, and ensuring adherence to regulatory and sponsor requirements. The EDC Coordinator will work closely with the site staff to optimize electronic data workflows and maintain data...

Job SummaryThis position is responsible for configuring, managing, and supporting clinical research teams in data entry and validation, and ensuring adherence to regulatory and sponsor requirements. The EDC Coordinator will work closely with the site staff to optimize electronic data workflows and maintain data integrity.Duties/ResponsibilitiesSupport...

**Key Responsibilities**: 1. **Inbound Requirement Management**: a. Handle current domestic and international placement requirements for paramedical and nursing professionals. 2. **Prospect Development**: a. Research and identify new opportunities for placements in emerging markets or healthcare sectors. b. Build and maintain strong relationships with...