Clinical Research Documentation Specialist

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...

Clinical Research Associate Position OverviewWe are seeking a highly motivated and organized Clinical Research Associate to join our team in a structured, accredited environment.Key Responsibilities:Support the coordination of clinical trial activities under close supervision.Maintain accurate records, site files, and case report forms.Collaborate with 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 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...

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...

Job Profile: Technical Documentation SpecialistWe are seeking a detail-oriented and organized Technical Documentation Specialist to join our team. The ideal candidate will have a strong foundation in writing and be able to translate complex technical information into clear, concise documentation.Key responsibilities include:Creating user manuals, guides, and...

We are seeking a Clinical Systems Tester to join our team.Job DescriptionClinical Systems Testers play a vital role in the development and implementation of clinical trials. They ensure that all systems are functioning correctly and as expected, while also identifying potential issues before they become major problems.Key Responsibilities:Author and execute...

Job Title: Senior Clinical Data Coordinator">Key Responsibilities:">">Coordinate document-related activities across projects and departments.">Review and maintain accurate documentation for clinical projects.">Ensure data integrity and compliance with regulatory requirements.">Provide support and training to team members as needed.">">About the Role:">The...

Job OverviewThe Associate Site Report Specialist plays a pivotal role in ensuring that Site Visit Reports (SVRs) adhere to quality standards and align with the organization's objectives of quality, subject safety, data integrity and regulatory compliance.This specialist oversees a caseload of SVRs for assigned studies, guaranteeing adherence to the protocol,...