As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Clinical Trial Rater
Houston, TX · Remote
Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...
Clinical Trial Rater
Houston, TX · Remote
Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Quick apply
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...
Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...
Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...
CRA II
Houston, TX · Remote
$91K - $114K/yr
CRA II (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research ... Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
CRA II
Houston, TX · Remote
$91K - $114K/yr
CRA II (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research ... Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
CRA II
Houston, TX · Remote
$91K - $114K/yr
CRA II (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research ... Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Quick apply
CRA II
Houston, TX · Remote
$91K - $114K/yr
CRA II (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research ... Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Clinicia Expert - Remote
Houston, TX · Remote
$150 - $200/hr
Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...
Quick apply
Clinicia Expert - Remote
Houston, TX · Remote
$150 - $200/hr
Clinician Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...
Biostatistician Expert - Remote
Houston, TX · Remote
$60 - $70/hr
Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced ... Analyze and validate clinical trial data. * Review and interpret Statistical Analysis Plans (SAPs)
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Biostatistician Expert - Remote
Houston, TX · Remote
$60 - $70/hr
Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced ... Analyze and validate clinical trial data. * Review and interpret Statistical Analysis Plans (SAPs)
Hematology Expert - Remote
Houston, TX · Remote
$150 - $200/hr
Hematology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...
Quick apply
Hematology Expert - Remote
Houston, TX · Remote
$150 - $200/hr
Hematology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...
Oncology Expert - Remote
Houston, TX · Remote
$150 - $200/hr
Oncology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...
Quick apply
Oncology Expert - Remote
Houston, TX · Remote
$150 - $200/hr
Oncology Expert Remote Job Type: Contractor Location: Remote Job Overview We are seeking ... Analyze clinical study reports, safety reports, regulatory documents, and trial materials to assess ...
Clinician (Oncology / Hematology) Expert - Remote
Houston, TX · Remote
$160 - $200/hr
Remote Job Overview We are looking for experienced Oncology and Hematology Clinicians to support an ... You will review clinical content, evaluate trial data, and provide expert medical insights to help ...
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Clinician (Oncology / Hematology) Expert - Remote
Houston, TX · Remote
$160 - $200/hr
Remote Job Overview We are looking for experienced Oncology and Hematology Clinicians to support an ... You will review clinical content, evaluate trial data, and provide expert medical insights to help ...
This role is responsible for clinical trial strategies within the US and EU regions for Danaher ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...
New
This role is responsible for clinical trial strategies within the US and EU regions for Danaher ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...
New
Associate Sampling Oversight Manager
Houston, TX · Remote
$95K - $130K/yr
Remote Salary Range: $95,000 to $130,000 Basic Qualifications: * Bachelor's degree in ... Track of all clinical trial samples from sample collection until destruction, including clinical ...
New
Associate Sampling Oversight Manager
Houston, TX · Remote
$95K - $130K/yr
Remote Salary Range: $95,000 to $130,000 Basic Qualifications: * Bachelor's degree in ... Track of all clinical trial samples from sample collection until destruction, including clinical ...
New
Maintaining our company culture across all regions, and especially with our remote employees, is ... trial-related material. * Maintains tracking records for assigned sites including tracking of ...
Maintaining our company culture across all regions, and especially with our remote employees, is ... trial-related material. * Maintains tracking records for assigned sites including tracking of ...
Medical Writer - AI Trainer
Houston, TX · Remote
$90 - $150/hr
Remote Commitment: 20-25 hours/week Role Responsibilities * Generate and validate high-quality, synthetic clinical trial data. * Author full CSR sections and design prompts, golden outputs, and ...
Quick apply
Medical Writer - AI Trainer
Houston, TX · Remote
$90 - $150/hr
Remote Commitment: 20-25 hours/week Role Responsibilities * Generate and validate high-quality, synthetic clinical trial data. * Author full CSR sections and design prompts, golden outputs, and ...
Financial Clearance Coordinator
Houston, TX · Remote
$42.79 - $53.37/hr
Preferred qualifications include research and clinical trial knowledge, authorization experience ... Remote but must be able to come onsite as needed. Why Us. At UT MD Anderson, this role directly ...
Financial Clearance Coordinator
Houston, TX · Remote
$42.79 - $53.37/hr
Preferred qualifications include research and clinical trial knowledge, authorization experience ... Remote but must be able to come onsite as needed. Why Us. At UT MD Anderson, this role directly ...
... ICON is a global healthcare intelligence and clinical research organisation united by a mission to ... SB7 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...
... ICON is a global healthcare intelligence and clinical research organisation united by a mission to ... SB7 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...
On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site ...
On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site ...
Freelance Independent Rater
Houston, TX · Remote
$62K - $156K/yr
... clinical trial experience and expertise in psychiatric assessments? We are expanding our global network of Central Independent Raters (CIRs) to support a depression study. 100% Remote Flexible ...
Freelance Independent Rater
Houston, TX · Remote
$62K - $156K/yr
... clinical trial experience and expertise in psychiatric assessments? We are expanding our global network of Central Independent Raters (CIRs) to support a depression study. 100% Remote Flexible ...
Freelance Independent Rater
Houston, TX · Remote
$62K - $156K/yr
... clinical trial experience and expertise in psychiatric assessments? We are expanding our global network of Central Independent Raters (CIRs) to support a depression study. 100% Remote Flexible ...
Freelance Independent Rater
Houston, TX · Remote
$62K - $156K/yr
... clinical trial experience and expertise in psychiatric assessments? We are expanding our global network of Central Independent Raters (CIRs) to support a depression study. 100% Remote Flexible ...
Remote Icon Clinical Trial information
See Spring, TX salary details
$25.67 - $31.11
4% of jobs
$31.11 - $36.56
6% of jobs
$36.56 - $42.01
7% of jobs
$46.09 is the 25th percentile. Wages below this are outliers.
$42.01 - $47.45
9% of jobs
$47.45 - $52.90
15% of jobs
The median wage is $55.30 / hr.
$52.90 - $58.34
18% of jobs
$62.22 is the 75th percentile. Wages above this are outliers.
$58.34 - $63.79
21% of jobs
$63.79 - $69.23
7% of jobs
$69.23 - $74.68
6% of jobs
$74.68 - $80.12
3% of jobs
$80.12 - $85.57
2% of jobs
$25
$55
$85
How much do remote icon clinical trial jobs pay per hour?
What is the difference between Remote Icon Clinical Trial vs Remote Clinical Research Coordinator?
| Aspect | Remote Icon Clinical Trial | Remote Clinical Research Coordinator |
|---|---|---|
| Credentials | Typically requires clinical trial experience, knowledge of ICON protocols, and relevant certifications | Requires clinical research experience, certification (e.g., CCRP), and understanding of study protocols |
| Work Environment | Primarily remote, collaborating with ICON's global teams and sponsors | Mostly remote or hybrid, coordinating study activities and communication with sites and sponsors |
| Employer & Industry | ICON, clinical research industry, pharmaceutical and biotech sectors | Research institutions, CROs, pharmaceutical companies, clinical trial industry |
Remote Icon Clinical Trial roles focus on managing and overseeing clinical trials within ICON, often requiring specific protocol knowledge. Remote Clinical Research Coordinators handle site activities, patient recruitment, and data collection, with a broader focus on trial execution. Both roles are remote-friendly but differ in responsibilities and required experience.
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Cities near Spring, TX with the most Remote Icon Clinical Trial job openings:
Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 6 days ago
Job description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
What You Will Do:
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile:
You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
- Willingness to travel as required (approximately 60%)
#LI-LB1 #LI-REMOTE
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- 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
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.
Are you a current ICON Employee? Please click here to apply