Knowledge of ICH-GCP guidelines jobs

Barcelona, Catalonia, Spain

Clinical Research Associate 1

ICON plc · Posted Nov 11, 2026

Barcelona, Catalonia, Spain

Clinical Research Associate

ICON plc · Posted Nov 11, 2026

Blue Bell, United States

Knowledge of ICH-GCP guidelines Ability to review and evaluate medical data Strong oncology experience

Clinical Research Associate responsible for monitoring clinical trials, coordinating study activities, and ensuring compliance with protocols and regulations.

Responsibilities

Deliver clinical trial monitoring work
Coordinate all activities for setting up and monitoring a study
Complete accurate study status reports
Maintain study documentation
Run sponsor generated queries

Requirements

University degree in medicine, science, or equivalent
Nice to have: Phase I experience

Skills

Benefits

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources

CRA II

ICON plc · Posted Nov 10, 2026

Long Beach, California, United States
Full-time · Associate
$91K–$114K per year
2+ years

clinical trial monitoring experience knowledge of ICH-GCP guidelines protocol compliance data integrity patient safety

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

Compensation

$91,336.00-$114,170.00

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
Contribute to the preparation and review of study documentation, including protocols and clinical study reports

Requirements

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

Skills

Clinical Research Associate I

ICON plc · Posted Nov 9, 2026

Beijing, China

Knowledge of ICH-GCP guidelines Review and evaluate medical data Excellent written and verbal communication in English Good social skills enabling timely query handling

Clinical Research Associate I

Responsibilities

Deliver clinical trial monitoring work to a high standard
Coordinate all activities for setting up and monitoring a study
Complete accurate study status reports and maintain study documentation
Run sponsor generated queries efficiently
Participate in preparation and review of study documentation and feasibility studies

Requirements

University degree in medicine, science, or equivalent

Skills

Benefits

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources

CRA I, CRA II and Senior CRA

ICON plc · Posted Nov 9, 2026

Tokyo, Tokyo, Japan

Knowledge of ICH-GCP guidelines Review and evaluate medical data Excellent written and verbal communication in English Good social skills

Clinical Research Associate responsible for monitoring clinical trials, coordinating study activities, and ensuring compliance with protocols and regulations.

Responsibilities

Deliver clinical trial monitoring work to high standard
Coordinate all activities for setting up and monitoring a study
Complete accurate study status reports and maintain study documentation
Run sponsor generated queries efficiently
Participate in preparation and review of study documentation and feasibility studies

Requirements

University degree in medicine, science, or equivalent

Skills

Benefits

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources

Clinical Research Associate

ICON plc · Posted Nov 9, 2026

Milan, Italy
€37K–€47K per year
1+ years

Knowledge of ICH-GCP guidelines Review and evaluate medical data Excellent written and verbal communication in English Good social skills enabling you to deal with queries in a timely manner Willingness to travel as required (approximately 60%)

Clinical Research Associate

Compensation

Salary Range €37,224.00-€46,530.00

Responsibilities

Deliver clinical trial monitoring work to a high standard
Coordinate all activities for setting up and monitoring a study
Complete accurate study status reports and maintain study documentation
Run sponsor generated queries efficiently
Participate in preparation and review of study documentation and feasibility studies for new proposals

Requirements

University degree in medicine, science, or equivalent

Skills

Histologist

ICON plc · Posted Nov 6, 2026

United States

Pathology lab experience Knowledge of ICH-GCP guidelines Medical data review

Histologist trained as a CRA I to support clinical trial monitoring and documentation.

Responsibilities

Deliver clinical trial monitoring work
Coordinate study setup and monitoring
Complete study status reports
Maintain study documentation
Run sponsor generated queries

Requirements

University degree in medicine, science

Skills

Benefits

Competitive base salary
Performance related incentives
Health and wellbeing programmes
Medical, dental, vision coverage
Retirement and pension plans

Histologist

ICON plc · Posted Nov 6, 2026

United States
Entry

Pathology Lab experience Knowledge of ICH-GCP guidelines

Histologist to train as a CRA I in clinical trial monitoring

Responsibilities

Deliver clinical trial monitoring work
Coordinate activities for setting up and monitoring a study
Complete accurate study status reports and maintain study documentation
Run sponsor generated queries efficiently
Participate in preparation and review of study documentation and feasibility studies

Requirements

University degree in medicine, science

Skills

Benefits

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources

Clinical Research Associate

ICON plc · Posted Nov 6, 2026

Miami, Florida, United States
Mid
2+ years