SIGN IN
Clinical Data Specialist jobs in United States
cer-icon
Apply on Employer Site
company-logo

Dexian · 12 hours ago

Clinical Data Specialist

Dexian is a leading provider of staffing, IT, and workforce solutions. The Clinical Data Specialist is responsible for coordinating data management activities across multiple studies and contributing to data management process improvements within the clinical data management lifecycle.
ConsultingHuman ResourcesInformation TechnologyProfessional ServicesStaffing Agency
check
H1B Sponsor Likelynote
Hiring Manager
Vikash Singh
linkedin

Responsibilities

Assist with the creation and/or review study-specific Case Report Forms (CRFs) using device study knowledge and protocol specific information in collaboration with clinical team
As applicable, contribute to the development of Case Report Form Library of common forms that can be used consistently across studies
Support EDC database development(s)
Participate in the validation and User Acceptance Testing (UAT) of EDC databases
Develop and/or review study-specific data management and database documentation, which may include Data Management Plan (DMP), CRF Completion Guidelines (CCGs), Annotated CRFs, Edit/Logic Check Specifications, and UAT Plans
Collaborate with clinical team members to generate data review guidelines and perform data review and query generation/closure
Prepare data for scheduled snapshots/database locks and perform archival activities upon study completion
Attend study-specific team meetings and produce requested metrics, which may include query information or data trends
Train Investigators and Coordinators on the EDC system, and CRF completion guidelines as needed
Manage EDC user access for sponsor and site personnel

Qualification

Clinical data managementEDC experienceClinical Practices (GCP)FDA regulationsMS Windows proficiencyOrganizational skillsCommunication skillsAttention to detailWork independently

Required

Bachelor's degree is strongly preferred
Requires 2+ years of clinical data and EDC experience
Strong computer skills with a proficiency with MS Windows based applications
Working knowledge of Good Clinical Practices (GCP), FDA regulations, and current industry practices related to the conduct of clinical trials including applicable ISO regulations for any trials conducted globally

Preferred

Able to prioritize workload, assign realistic completion dates, and complete assignments on schedule
Excellent written and oral communications skills required
Comfortable with multiple Electronic Data Capture (EDC) Systems
Strong organizational skills and attention to detail
Ability to work independently and manage multiple tasks in a fast-paced, changing environment
Medical Devices preferred

Company

Dexian provides services for staffing, talent development, and consulting, with a focus on technology, finance, and project management.

H1B Sponsorship

Dexian has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (65)

Funding

Current Stage
Late Stage

Leadership Team

leader-logo
Mahfuz Ahmed
Chairman of the Board
linkedin
leader-logo
Vikram Motiani
Managing Director, APAC
linkedin
Company data provided by crunchbase