Electronic data capture system jobs

Senior Clinical Study Manager

Intuitive · Posted Nov 5, 2026

Open

Sunnyvale, California, United States
Senior
5+ years

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Senior Clinical Study Manager

Intuitive · Posted Nov 5, 2026

Open

Sunnyvale, California, United States
Senior
5+ years

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Clinical Research Associate 1

Hologic Careers · Posted Nov 5, 2026

Open

San Diego, California, United States
Hybrid
Full-time · Entry
$74K–$102K per year
1–2 years

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The Clinical Research Associate 1 (CRA 1) conducts site monitoring/management activities in accordance with regulations and department plans and procedures. Monitoring activities may be conducted in-house or by visiting sites.

Compensation

The annualized base salary range for this role is $73,500 to $101,500 and the position is eligible for an annual bonus.

Responsibilities

Conducts Site Qualification, Initiation, Interim Monitoring, Close-Out visits and activities in accordance with FDA Code of Federal Regulations, Good Clinical Practice, guidelines, departmental procedures and the Clinical Monitoring Plan (CMP)
Ensures records are complete and consistent with governing regulations
Able to use or uses electronic data capture system and other monitoring tools to review and ensure accurate and complete clinical data collection
Assists sites with site-level IRB submissions, queries and documentation
Establishes and maintains regular communication with clinical sites

Requirements

BA degree
BS degree
Nice to have: Experience with In Vitro Diagnostic (IVD) clinical studies

Skills

Working knowledge of clinical trial practices and regulations Working knowledge of clinical trial monitoring and site management

Clinical Research Assistant I - CIBMTR

Medical College of Wisconsin · Posted Nov 4, 2026

Open

Milwaukee, Wisconsin, United States
On-site
Full-time · Entry

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Provide research and administrative support for clinical research programs focused on patient-reported outcomes (PROs), quality of life, and patient experiences. Assist with qualitative and quantitative research activities.

Responsibilities

Assist with literature searches, literature reviews, and scoping reviews, including article screening, data extraction, and summarizing research findings.
Assist with research dissemination, including preparing abstracts, posters, presentations, manuscripts, and reports.
Assist with study coordination, data entry, data quality checks, and maintaining accurate research records and databases.
Ensures accurate entry of responses into electronic data capture system.
Maintains confidentiality of all data in accordance with NMDP policies, while having access to PII, PHI and study-data for each research subject.

Requirements

High school or equivalent
Nice to have: Medical terminology

Skills

MS Office word processing spreadsheet software database software application

Clinical Research Coordinator 2

UOMUOMUS · Posted Oct 19, 2026

Open

Miami, Florida, United States
On-site
Full-time · Mid
2+ years

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Mid-level clinical research professional coordinating and implementing ophthalmology studies at the McKnight Vision Research Center.

Compensation

The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.

Responsibilities

Assist in participant recruitment and retention
Perform study procedures and data collection
Collect, process, pack, and ship specimens
Maintain study binders and filings
Distribute study drug materials

Requirements

Bachelor’s degree in relevant field

Skills

clinical research coordination protocol implementation data collection specimen handling regulatory compliance study documentation communication

Clinical Research Coordinator I

ALLIANCE CLINICAL LLC · Posted Nov 3, 2026

Open

Buffalo, New York, United States +1 more
Full-time · Entry
2+ years

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Supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines.

Locations (2)

Buffalo, New York, United States
Tonawanda, New York, United States

Responsibilities

Communicate clearly and professionally with study participants regarding study objectives and ongoing instructions.
Adhere to site standard operating procedures (SOPs).
Administer questionnaires and monitor participant compliance with study protocols.
Respond to participant needs promptly and appropriately.
Collect and document patient medical history and health conditions.

Requirements

Associate's degree in healthcare or a related field, or equivalent relevant experience

Skills

phlebotomy

Senior Clinical Study Manager

Senior Clinical Study Manager

Responsibilities

Requirements

Skills

Clinical Research Associate 1

Compensation

Responsibilities

Requirements

Skills

Clinical Research Assistant I - CIBMTR

Responsibilities

Requirements

Skills

Clinical Research Coordinator 2

Compensation

Responsibilities

Requirements

Skills

Clinical Research Coordinator I

Locations (2)

Responsibilities

Requirements

Skills

Benefits

Benefits

Benefits