Clinical Research Document Specialist

As a Clinical Research Associate, you will play a crucial role in the success of clinical trials.Key Responsibilities:Author and analyze clinical trial documents, including protocols, informed consent forms, and clinical study reports.Ensure accuracy and compliance with global regulatory standards (FDA, EMA, ICH-GCP).Create, validate, and refine prompts for...

Clinical Research ProfessionalWe are offering an exceptional career opportunity for recent graduates to launch their careers in clinical research.This position is exclusively open to freshers. Candidates with prior experience are not eligible for this role.Key Responsibilities:Assist with on-site coordination of clinical trial activities under...

Medical Professional OpportunityDenvax Cancer Center, Vasant Vihar, New DelhiAbout UsWe are India's pioneers in dendritic cell cancer immunotherapy. Our state-of-the-art facility houses a nursing home with an ICU unit, delivering advanced, patient-centered care exclusively to cancer patients.Job SummaryWe are seeking a highly skilled medical professional to...

Senior Clinical Operations ManagerJob Overview:Lead global unblinded CRA teams and provide technical support for unblinded clinical operations.Key Responsibilities:Implement effective recruitment strategies to meet project recruitment targets.Contribute to risk mitigation plans and manage clinical risks throughout the project lifecycle.Ensure clinical...

Clinical Data Management Specialist Job OverviewThis position is responsible for defining project specifications for data management services.The successful candidate will understand external data collection, integration into clinical trials, and the necessary reconciliation processes to ensure accuracy and relevance.

Business AnalystWe are seeking a seasoned Business Analyst with 5-8 years of experience in the Life Sciences domain, focusing on Clinical Trials and Clinical Operations.The ideal candidate will have hands-on experience with clinical trial systems and have played a key role in 2-3 end-to-end technology implementations across the clinical trials value...

Medical Data SpecialistOur organization seeks a Medical Data Specialist to support the development of artificial intelligence (AI) and machine learning (ML) models in ophthalmology. The role involves utilizing clinical expertise to annotate and label medical data, primarily images and structured clinical data related to eye health.Responsibilities:Data...

Job Title: Quality Assurance ProfessionalKey Responsibilities:Serve as primary quality support resource for clinical study teams.Provide expertise during protocol deviation meetings, risk-based quality management discussions.Write and review standard operating procedures and other quality documentation.Manage quality processes in Veeva QMS.Address QA-related...

Job Opportunity: We are seeking an experienced Clinical Systems Tester to join our team.Key Responsibilities:Author and execute test scripts in Veeva EDC, aligned with protocol requirementsValidate workflows across eCOA and IRT platformsParticipate in system validation (IQ/OQ/PQ, UAT) for DCT tools including handheld and remote-use devicesCollaborate with...

Job Overview:The Senior Clinical Data Coordinator role is responsible for overseeing project-specific and departmental document management activities.Main Responsibilities:Evaluates project-specific documents to ensure compliance with applicable rules, regulations, guidelines, standard operating procedures (SOPs), and policies.Coordinates database design...