Manage risk assessment and execution; * Responsible for management of study vendor; and * Manage ... Office based environment with on-site mentors * Defined career paths with clear advancement ...
Manage risk assessment and execution; * Responsible for management of study vendor; and * Manage ... Office based environment with on-site mentors * Defined career paths with clear advancement ...
Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based) Serving as a value-added resource and extension of the Company, the Clinical Trial Liaison (CTL) will support the Company ...
Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based) Serving as a value-added resource and extension of the Company, the Clinical Trial Liaison (CTL) will support the Company ...
Associate Director, Clinical Trial Activations
$59.13 - $74.04/hr
The primary purpose of this Associate Director, Clinical Trial Activations is to provide direct ... Monitor the quality, timeliness, and consistency of staff communications and guidance. Plan and ...
Associate Director, Clinical Trial Activations
$59.13 - $74.04/hr
The primary purpose of this Associate Director, Clinical Trial Activations is to provide direct ... Monitor the quality, timeliness, and consistency of staff communications and guidance. Plan and ...
The primary purpose of this Associate Director, Clinical Trial Activations is to provide direct ... Monitor the quality, timeliness, and consistency of staff communications and guidance. • Plan and ...
The primary purpose of this Associate Director, Clinical Trial Activations is to provide direct ... Monitor the quality, timeliness, and consistency of staff communications and guidance. • Plan and ...
Associate Director, Clinical Trial Activations
Houston, TX · On-site
$59.13 - $74.04/hr
The primary purpose of this Associate Director, Clinical Trial Activations is to provide direct ... Monitor the quality, timeliness, and consistency of staff communications and guidance. • Plan and ...
Associate Director, Clinical Trial Activations
Houston, TX · On-site
$59.13 - $74.04/hr
The primary purpose of this Associate Director, Clinical Trial Activations is to provide direct ... Monitor the quality, timeliness, and consistency of staff communications and guidance. • Plan and ...
Associate Director, Clinical Trial Activations
$59.13 - $74.04/hr
The primary purpose of this Associate Director, Clinical Trial Activations is to provide direct ... Monitor the quality, timeliness, and consistency of staff communications and guidance. • Plan and ...
Associate Director, Clinical Trial Activations
$59.13 - $74.04/hr
The primary purpose of this Associate Director, Clinical Trial Activations is to provide direct ... Monitor the quality, timeliness, and consistency of staff communications and guidance. • Plan and ...
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 ...
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 ...
Associate Clinical Trial Manager - PhD - Immunology - Dallas
Irving, TX · On-site
$31 - $42.50/hr
... based Associate Clinical Trial Manager (aCTM) position in our Dallas, TX office. The aCTM is part ... of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers ...
Associate Clinical Trial Manager - PhD - Immunology - Dallas
Irving, TX · On-site
$31 - $42.50/hr
... based Associate Clinical Trial Manager (aCTM) position in our Dallas, TX office. The aCTM is part ... of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers ...
Associate Clinical Trial Manager - PhD - Immunology - Dallas
Irving, TX · On-site +1
$31 - $42.50/hr
... based Associate Clinical Trial Manager (aCTM) position in our Dallas, TX office. The aCTM is part ... of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers ...
Associate Clinical Trial Manager - PhD - Immunology - Dallas
Irving, TX · On-site +1
$31 - $42.50/hr
... based Associate Clinical Trial Manager (aCTM) position in our Dallas, TX office. The aCTM is part ... of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Dallas
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Dallas
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Houston, TX · On-site +1
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 ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Houston, TX · On-site +1
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 ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Dallas, TX · On-site +1
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 ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Dallas, TX · On-site +1
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 ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Austin, TX · On-site +1
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 ...
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Austin, TX · On-site +1
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 ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Dallas
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology - Dallas
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Ophthalmology for a full-time, office-based Associate Clinical Trial Manager (aCTM ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Dallas
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Infectious Disease areas for a full-time, office-based Associate Clinical Trial ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Dallas
Irving, TX · On-site
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Infectious Disease areas for a full-time, office-based Associate Clinical Trial ...
Associate Clinical Trial Manager - PhD - Metabolic - Dallas, TX
Irving, TX · On-site +1
$31 - $42.50/hr
... based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical ...
Associate Clinical Trial Manager - PhD - Metabolic - Dallas, TX
Irving, TX · On-site +1
$31 - $42.50/hr
... based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical ...
Associate Clinical Trial Manager - PhD - Metabolic - Dallas, TX
Irving, TX · On-site
$31 - $42.50/hr
... based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical ...
Associate Clinical Trial Manager - PhD - Metabolic - Dallas, TX
Irving, TX · On-site
$31 - $42.50/hr
... based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Dallas
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Infectious Disease areas for a full-time, office-based Associate Clinical Trial ...
Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Dallas
Irving, TX · On-site +1
$31 - $42.50/hr
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Infectious Disease areas for a full-time, office-based Associate Clinical Trial ...
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 ...
Clinical Trial Risk Based Monitoring information
What is clinical trial risk based monitoring?
How does a clinical trial risk based monitoring professional typically collaborate with cross-functional teams during a study?
What are the key skills and qualifications needed to thrive in clinical trial risk based monitoring, and why are they important?
What is the difference between Clinical Trial Risk Based Monitoring vs Clinical Trial Data Manager?
| Aspect | Clinical Trial Risk Based Monitoring | Clinical Trial Data Manager |
|---|---|---|
| Primary Focus | Monitoring trial sites for risks and compliance | Managing and ensuring accuracy of trial data |
| Required Skills | Monitoring protocols, regulatory knowledge, site management | Data management, database systems, quality control |
| Work Environment | Clinical sites, monitoring visits, remote oversight | Data centers, clinical trial databases, office setting |
| Certifications | GCP, monitoring certifications | CDMP, data management certifications |
While both roles are integral to clinical trials, Risk Based Monitoring focuses on overseeing site performance and compliance to mitigate risks, whereas Data Managers concentrate on managing and validating trial data for accuracy and integrity.
What are popular job titles related to Clinical Trial Risk Based Monitoring jobs in Texas?
For Clinical Trial Risk Based Monitoring jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Risk Based Monitoring jobs in Texas look for?
The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Texas are:
What cities in Texas are hiring for Clinical Trial Risk Based Monitoring jobs?
Cities in Texas with the most Clinical Trial Risk Based Monitoring job openings:

Clinical Trial Project Manager - Infectious Diseases - Dallas
Irving, TX • On-site, Remote
Full-time
Medical, Retirement, PTO
Re-posted 10 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
13th of 73 rated research
Job description
Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Infectious Diseases to join our Clinical Trial Management Group at our Dallas, TX office. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
Responsibilities- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations;
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables;
- Maintain in depth knowledge of protocol, therapeutic area, and indication;
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided;
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable;
- Develop operational project plans;
- Manage risk assessment and execution;
- Responsible for management of study vendor; and
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
- Bachelor's degree in a health-related field; Advanced degree in a health-related field preferred;
- Experience in Phases 1-4; Phases 2-3 preferred;
- 3-5 years as a project/clinical trial manager within a CRO;
- Management of overall project timeline; and
- Strong leadership skills.
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
-
- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
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- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
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- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
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- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Employment Type: OTHERAbout Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992