Distributed Clinical Trials Tester

Launch Your Clinical Research CareerWe are seeking a highly motivated and detail-oriented individual to fill the role of Clinical Research Associate. This is an excellent opportunity for fresh graduates to launch their careers in clinical research.Key Responsibilities:Assist with on-site coordination of clinical trial activities under supervisionMaintain...

Job Title:Clinical Data Management SpecialistAt our organization, we are seeking a highly skilled Clinical Data Management Specialist to join our team. In this role, you will be responsible for managing and analyzing clinical trial data to ensure accuracy, relevance, and compliance with industry standards.Key Responsibilities:Define project specifications...

Healthcare Screening ProfessionalWe are seeking skilled healthcare professionals to conduct clinical trial screening interviews on a freelance basis.Candidates will be responsible for contacting volunteers within 48 hours of their registration, conducting scripted interviews, and receiving paid training.Your role involves contacting candidates, conducting...

Job DescriptionSponsor-dedicated professionals are at the heart of our clients' innovation, driving the next generation of patient treatment. As a Senior Statistical Programmer, you'll work embedded within one of our pharmaceutical clients, supported by Cytel's team.Position Overview: This role will involve leveraging advanced SAS programming skills and...

Job Title: Clinical Systems TesterWe are seeking an experienced and skilled professional to support the development of clinical systems in a decentralized environment. As a Clinical Systems Tester, you will be responsible for testing and validating activities across various digital systems and patient-facing technologies.Main Responsibilities:Author and...

Key Clinical Trial Documents SpecialistAs a Key Clinical Trial Documents Specialist, you will be responsible for developing high-quality clinical trial documents. This includes protocols, Investigator's Brochures, Informed Consent Forms, Case Report Forms, and Clinical Study Reports.ResponsibilitiesTranslate complex scientific data into clear, regulatory...

Job Opportunity: Quality Assurance ProfessionalWe are seeking an experienced professional to provide day-to-day clinical quality assurance support across ongoing clinical trials. The ideal candidate brings strong experience with Veeva QMS, is highly tech-savvy, and can support clinical operations teams in a fast-paced environment.The primary QA support...

Overview:We are seeking a skilled professional to join our team as a Clinical Data Management Specialist.About the Role:This is an exciting opportunity for a motivated and detail-oriented individual to take on a challenging role in data management.Key Responsibilities:Data Management Services: Define project specifications for Data Management services,...

Job OpportunityWe are seeking an experienced quality assurance professional to provide day-to-day clinical quality assurance support across ongoing clinical trials. The ideal candidate brings strong experience with Veeva QMS, is highly tech-savvy, and can support clinical operations teams in a fast-paced environment.Key ResponsibilitiesServe as the primary...

About Us:We are a leading provider of digital engineering and IT services.Our expertise combines deep industry knowledge with agile development practices, enabling scalable and cost-effective solutions for our clients.Job Title: Clinical Document AuthorKey Responsibilities:Author and analyze clinical trial documents.Work with key clinical documents:...