Senior CRA
Houston, TX · On-site
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 ...
Quick apply
Houston, TX · On-site
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 ...
Quick apply
Houston, TX · On-site
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 ...
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 ...
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 ...
Houston, TX · On-site
Under the direction of Research Nurse/Clinical Trial Manager/Physician, captures and reports Adverse Events (A/E) or Serious Adverse Events (SAE) to necessary regulatory authorities. * Assists ...
Houston, TX · On-site
Under the direction of Research Nurse/Clinical Trial Manager/Physician, captures and reports Adverse Events (A/E) or Serious Adverse Events (SAE) to necessary regulatory authorities. * Assists ...
Houston, TX · On-site
Under the direction of Research Nurse/Clinical Trial Manager/Physician, captures and reports Adverse Events (A/E) or Serious Adverse Events (SAE) to necessary regulatory authorities. * Assists ...
Houston, TX · On-site
Under the direction of Research Nurse/Clinical Trial Manager/Physician, captures and reports Adverse Events (A/E) or Serious Adverse Events (SAE) to necessary regulatory authorities. * Assists ...
Houston, TX · On-site
Under the direction of Research Nurse/Clinical Trial Manager/Physician, captures and reports Adverse Events (A/E) or Serious Adverse Events (SAE) to necessary regulatory authorities. * Assists ...
Houston, TX · On-site
Under the direction of Research Nurse/Clinical Trial Manager/Physician, captures and reports Adverse Events (A/E) or Serious Adverse Events (SAE) to necessary regulatory authorities. * Assists ...
By managing complex contracts and financial operations with precision, the role supports clinical ... Department Specific Criteria * Direct experience in clinical trial billing and account ...
By managing complex contracts and financial operations with precision, the role supports clinical ... Department Specific Criteria * Direct experience in clinical trial billing and account ...
Creates and maintains records of IRB submissions, approvals, and expiration dates for all study sites (e.g. in electronic clinical trial management system). Performs Activation checks and activates ...
Creates and maintains records of IRB submissions, approvals, and expiration dates for all study sites (e.g. in electronic clinical trial management system). Performs Activation checks and activates ...
You will serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I), overseeing clinical trial activities and ensuring the highest standards of patient safety and protocol compliance across ...
You will serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I), overseeing clinical trial activities and ensuring the highest standards of patient safety and protocol compliance across ...
Federal Work Study Student, Clinical Laboratory Sciences Galveston, Texas, United States Student Titles UTMB Health Requisition # 2506590 Minimum Qualifications: High School Diploma, UTMB Student ...
Federal Work Study Student, Clinical Laboratory Sciences Galveston, Texas, United States Student Titles UTMB Health Requisition # 2506590 Minimum Qualifications: High School Diploma, UTMB Student ...
Houston, TX · On-site
$28 - $65/hr
At Empathx, we drive equitable access to complex trials at any phase by providing industry-leading patient access, clinical trial management, and analysis across cardiology/nephrology, psychiatry ...
Quick apply
Houston, TX · On-site
$28 - $65/hr
At Empathx, we drive equitable access to complex trials at any phase by providing industry-leading patient access, clinical trial management, and analysis across cardiology/nephrology, psychiatry ...
Houston, TX · On-site
$70K - $83K/yr
Creates and maintains records of IRB submissions, approvals, and expiration dates for all study sites (e.g. in electronic clinical trial management system). Performs Activation checks and activates ...
Houston, TX · On-site
$70K - $83K/yr
Creates and maintains records of IRB submissions, approvals, and expiration dates for all study sites (e.g. in electronic clinical trial management system). Performs Activation checks and activates ...
Webster, TX · On-site
... and clinical trial opportunities to drive success · Daily use of our CRM platform (Hubspot) for business development activities and relationship management · Utilize sales techniques to pitch to ...
Webster, TX · On-site
... and clinical trial opportunities to drive success · Daily use of our CRM platform (Hubspot) for business development activities and relationship management · Utilize sales techniques to pitch to ...
Houston, TX · On-site
Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA ...
New
Houston, TX · On-site
Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA ...
New
Manages investigative site activity for multiple protocols / indications and provides ongoing ... trial-related material. * Maintains tracking records for assigned sites including tracking of ...
Manages investigative site activity for multiple protocols / indications and provides ongoing ... trial-related material. * Maintains tracking records for assigned sites including tracking of ...
Houston, TX · On-site
Management of Clinical Trial Patients * Provides complete patient assessment, including vital signs and pre-examination procedures * Gathers and assess objective and subjective data from the patient
Houston, TX · On-site
Management of Clinical Trial Patients * Provides complete patient assessment, including vital signs and pre-examination procedures * Gathers and assess objective and subjective data from the patient
Management of Clinical Trial Patients * Provides complete patient assessment, including vital signs and pre-examination procedures * Gathers and assess objective and subjective data from the patient
Management of Clinical Trial Patients * Provides complete patient assessment, including vital signs and pre-examination procedures * Gathers and assess objective and subjective data from the patient
Houston, TX · On-site
$97K - $116K/yr
... Clinical Trial Management Evaluate patient responses to protocol therapy Assess treatment toxicities and adverse drug reactions Report findings appropriately to the Principal Investigator ...
Houston, TX · On-site
$97K - $116K/yr
... Clinical Trial Management Evaluate patient responses to protocol therapy Assess treatment toxicities and adverse drug reactions Report findings appropriately to the Principal Investigator ...
Houston, TX · On-site
$111K - $130K/yr
Works in close coordination with Clinical Trial Finance, QA/QC, and Research Administration to ... Manages regulatory activities across the full clinical trial lifecycle, including study start-up ...
Houston, TX · On-site
$111K - $130K/yr
Works in close coordination with Clinical Trial Finance, QA/QC, and Research Administration to ... Manages regulatory activities across the full clinical trial lifecycle, including study start-up ...
Pasadena, TX · On-site
$20.75 - $27.50/hr
What You'll DoLead Clinical Trial Execution * Manage assigned clinical trials in accordance with protocol requirements, Good Clinical Practice (GCP), and site SOPs. * Review and understand study ...
Pasadena, TX · On-site
$20.75 - $27.50/hr
What You'll DoLead Clinical Trial Execution * Manage assigned clinical trials in accordance with protocol requirements, Good Clinical Practice (GCP), and site SOPs. * Review and understand study ...
... time management, and data interpretation skills. Collaboration with physicians, researchers, and clinical trial staff will enhance communication, teamwork, and professionalism, while presenting ...
... time management, and data interpretation skills. Collaboration with physicians, researchers, and clinical trial staff will enhance communication, teamwork, and professionalism, while presenting ...
$25.81 - $31.29
4% of jobs
$31.29 - $36.76
6% of jobs
$36.76 - $42.24
7% of jobs
$46.34 is the 25th percentile. Wages below this are outliers.
$42.24 - $47.71
9% of jobs
$47.71 - $53.19
15% of jobs
The median wage is $55.60 / hr.
$53.19 - $58.66
18% of jobs
$62.56 is the 75th percentile. Wages above this are outliers.
$58.66 - $64.14
21% of jobs
$64.14 - $69.61
7% of jobs
$69.61 - $75.09
6% of jobs
$75.09 - $80.56
3% of jobs
$80.56 - $86.04
2% of jobs
$25
$55
$86
A clinical trial manager, or CTM, oversees research and each phase of clinical drug tests at a hospital. They work closely with both the doctors and clinicians who are performing the trial, as well as the sponsor of the study, which is typically a pharmaceutical company or other health care organization. As a CTM, duties and responsibilities include planning and managing the trial, making sure that the test meets all government standards, and determining if it was successful. Clinical trial managers also hire, train, and evaluate the members of the clinical team.
The top searched job categories for Clinical Trial Manager jobs in Rosharon, TX are:
Cities near Rosharon, TX with the most Clinical Trial Manager job openings:

Full-time
Medical, Dental, Vision, Life, Retirement
Posted 29 days ago
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.
Experience in ophthalmology or gene therapy studies
Willingness to travel as required (approximately 60%, but must be flexible to travel as needed)
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:
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 request here.
Are you a current ICON Employee? Please click here to apply