Study documentation jobs

Data Compliance Coordinator

Thermo Fisher Scientific · Posted Nov 8, 2026

Open

Las Vegas, Nevada, United States
On-site
Associate

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Data Compliance Coordinator

Thermo Fisher Scientific · Posted Nov 8, 2026

Open

Las Vegas, Nevada, United States
On-site
Associate

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Sr. Clinical Operations Lead

Alimentiv · Posted Feb 19, 2026

Open

Boston, Massachusetts, United States
Senior
7–9 years

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Lead clinical operations oversight for regional and global trials, ensuring compliance and quality delivery across monitoring and site management activities.

Responsibilities

Provide regional and/or global clinical operations oversight across assigned studies
Lead and oversee Clinical Operations Leads (COLs) and CRAs
Oversee key monitoring and site management deliverables
Lead and support country and site feasibility, selection and start-up activities
Serve as a key liaison between monitoring team, Clinical Project Management, cross-functional study teams and Sponsors

Requirements

Bachelor’s degree in a relevant discipline
Nice to have: 10+ years of experience

Skills

clinical research CRA COL ICH-GCP clinical monitoring site management study start-up

Clinical Research Assistant

Tekton Research Inc · Posted Nov 7, 2026

Open

McKinney, Texas, United States
On-site
Full-time
0+ years

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Support clinical research team in daily operations of clinical trials, including patient interaction, study coordination, and data support.

Responsibilities

Support patient recruitment through pre-screening and scheduling
Prepare source documentation and visit binders for study visits
Request and manage medical records as needed
Ensure completion of e-diaries by study participants
Check patients in and out for study visits

Requirements

High school diploma or GED required
Some college or healthcare-related coursework preferred
Nice to have: Medical Assistant
Nice to have: EMT
Nice to have: clinical research experience

Skills

phlebotomy patient recruitment data entry medical records management EKG/ECG EDC systems study documentation

Clinical Research Associate 2

ICON plc · Posted Nov 6, 2026

Open

Madrid, Madrid, Spain
2+ years

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Clinical Research Associate II

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 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 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

Clinical Research, Clinical Safety Manager

Castle Biosciences · Posted Sep 15, 2026

Open

Remote, United States
Remote
Full-time
5+ years

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The Clinical Research Safety Manager is responsible for establishing, implementing, and continuously improving clinical research safety processes for a laboratory-developed test (LDT) and medical device organization while ensuring compliance with applicable regulations, Company policies, and Standard Operating Procedures (SOPs).

Compensation

Excellent Annual Salary + 20% Bonus Potential

Responsibilities

Establish and implement clinical research safety processes
Continuously improve safety processes
Ensure compliance with regulations and SOPs
Serve as operational safety lead for company-sponsored clinical studies
Oversee safety planning, adverse event management, risk assessments, safety reporting, and regulatory documentation

Requirements

Bachelor's degree in life sciences, nursing, clinical research, public health, regulatory affairs, quality assurance, or a related field

Skills

clinical research medical devices diagnostics regulatory affairs quality assurance

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