Study documentation jobs

Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolve queries to maintain high‑quality clinical data
Prepare and review study documentation, including protocols and clinical study reports

Requirements

Bachelor's degree in a scientific or healthcare‑related field

Skills

clinical trial monitoring protocol compliance data integrity ICH‑GCP guidelines site qualification initiation monitoring

CRA II

ICON plc · Posted Nov 6, 2026

Open

Remote, Thailand
Remote
Full-time
2+ years

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Clinical Research Associate II responsible for designing, analysing, and monitoring clinical trials.

Responsibilities

Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolution of queries to maintain high‑quality clinical data
Prepare and review study documentation, including protocols and clinical study reports

Requirements

Bachelor's degree in a scientific or healthcare‑related field

Skills

clinical trial monitoring site qualification initiation monitoring close‑out visits protocol compliance data integrity

Manager, Clinical Operations

Parexel · Posted Nov 6, 2026

Open

Bengaluru, Karnataka, India
On-site
Manager

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Lead and manage clinical research operations, overseeing project delivery, team performance, and regulatory compliance in a fast‑paced, growth‑oriented environment.

Responsibilities

Oversee project delivery and team performance
Resource client projects and staff assignments
Produce accurate resourcing plans
Develop action plans to keep projects on time and within budget
Recruit, retain, and develop a skilled team

Requirements

Degree level or equivalent nursing qualification or relevant clinical or other equivalent experience
Nice to have: degree in a biological science
Nice to have: pharmacy
Nice to have: oral English competency

Skills

clinical research data management ICH-GCP regulatory requirements study documentation quality control processes resourcing plans

Freelance Research Nurse – Home Visits

IQVIA · Posted Nov 5, 2026

Open

Amsterdam, North Holland, Netherlands
Contract

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Freelance Research Nurse conducting scheduled home visits for clinical research studies.

Responsibilities

Conduct scheduled visits in patient homes
Administer injection or infusion of study medication
Record vital signs and monitor patient
Perform blood draws if required
Review and report adverse events

Requirements

Registered Nurse
Nice to have: clinical research experience
Nice to have: home nursing experience

Skills

injection infusion blood draws phlebotomy vital sign monitoring study documentation IT skills various systems and platforms

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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 Trials Assistant

IQVIA · Posted Nov 3, 2026

Open

Amsterdam, North Holland, Netherlands +1 more
Hybrid

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Locations (2)

Amsterdam, North Holland, Netherlands
Haarlem, North Holland, Netherlands

Responsibilities

Maintain and update Trial Master Files (TMF) and study documentation.
Support document preparation, filing, tracking, and archiving.
Review study files for completeness and compliance.
Coordinate clinical trial supplies and tracking records.
Assist with CRF tracking, study queries, and data workflows.

Requirements

Science degree
Nice to have: Science degree
Nice to have: clinical research experience

Skills

TMF CRF Microsoft Office

Data Compliance Coordinator

Data Compliance Coordinator

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Requirements

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Clinical Research Assistant

Responsibilities

Requirements

Skills

Clinical Research Associate 2

Responsibilities

Requirements

Skills

CRA II

Responsibilities

Requirements

Skills

Manager, Clinical Operations

Responsibilities

Requirements

Skills

Freelance Research Nurse – Home Visits

Responsibilities

Requirements

Skills

Clinical Research Coordinator 2

Compensation

Responsibilities

Requirements

Skills

Clinical Trials Assistant

Locations (2)

Responsibilities

Requirements

Skills

Benefits

Benefits

Benefits