Clinical Data Specialist

Job Title:Clinical Data Management SpecialistJob Description:The clinical data management specialist plays a pivotal role in the success of clinical trials by ensuring the accuracy, quality, and integrity of trial data.This includes defining project specifications for data management services, including protocol conversion, database build, CRF design, and...

Medical Data Labeling SpecialistThis role requires a medical professional with expertise in ophthalmology to annotate visual data for the development and refinement of AI models.Responsibilities:Data Annotation: Review fundus images, OCT scans, and other visual data to identify anatomical structures and disease markers.Apply standardized grading protocols...

Clinical Nutrition SpecialistAt our organization, we're seeking an exceptional Clinical Nutrition Specialist who can drive patient wellness and sales of clinical products. This is a pivotal role that demands your enterprising spirit, health-tech acumen, and confidence in communicating with medical professionals.Key Responsibilities:Provide personalized...

Role: Clinical Data Scientist / Trial LeadKey ResponsibilitiesLead clinical data management activities across assigned clinical trials, ensuring high-quality data acquisition, database design, and data integrity.Act as a technical resource for Data Management (DM) and Risk-Based Monitoring (RBM) standards, tools, and reporting.Collaborate with...

Job OverviewYou'll be at the heart of our clients' innovation, leveraging advanced programming skills and proficiency in CDISC standards to drive clinical trials forward.Position Summary:This role will see you performing data manipulation, analysis, and reporting of clinical trial data, utilizing SAS programming. You'll also generate and validate SDTM and...

Key Clinical Trial Document DeveloperDevelop high-quality clinical trial documents, including protocols, investigator brochures, informed consent forms, case report forms, and clinical study reports.Key Responsibilities:Develop Key Documents: Protocols, IBs, ICFs, CRFs, CSRs, and other regulatory compliant documents that support drug development and approval...

Job Title: Data Scientist The Role:We are seeking a highly skilled and motivated Data Analyst with expertise in Python programming to join our team. As a key member of the data management team, you will be responsible for providing comprehensive clinical lab data expertise to develop and maintain Laboratory Data Management (LDM) tasks.Support the...

Job Opportunity: Clinical Lead RoleWe are seeking a highly skilled Clinical Lead to oversee global unblinded CRA teams and provide technical support for unblinded clinical operations.Key Responsibilities:Meet projects' recruitment targets by developing effective strategies.Contribute to project risk mitigation plans and manage clinical risks throughout the...

About Our Client:Our Client is a global IT services company headquartered in Southborough, Massachusetts. Founded in 1996, it specializes in digital engineering and IT services, helping clients modernize their technology infrastructure.Job Title: Clinical Document AuthoringSkills: Protocol , Informed Consent Form (ICF) , FDA , EMA , ICH-GCPBenefits:Hybrid...

Job OverviewWe are seeking an experienced Quality Assurance Specialist 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.As the primary QA support resource, ensure...