Bachelor's degree (science, business, or project management preferred) * 6-18 months clinical research experience or equivalent * 2+ years of project management experience * Ability to learn and use ...
Bachelor's degree (science, business, or project management preferred) * 6-18 months clinical research experience or equivalent * 2+ years of project management experience * Ability to learn and use ...
Bachelor's degree (science, business, or project management preferred) * 6-18 months clinical research experience or equivalent * 2+ years of project management experience * Ability to learn and use ...
Bachelor's degree (science, business, or project management preferred) * 6-18 months clinical research experience or equivalent * 2+ years of project management experience * Ability to learn and use ...
Senior IT Project Manager (onsite only)
Irving, TX · On-site
$121K - $122K/yr
Manage the performance and functions of assigned projects. * Plan, review and control the ... Prior healthcare technology and/or clinical project experience required
Senior IT Project Manager (onsite only)
Irving, TX · On-site
$121K - $122K/yr
Manage the performance and functions of assigned projects. * Plan, review and control the ... Prior healthcare technology and/or clinical project experience required
Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Project Managers with a focus on Neuroscience or CNS to join our Clinical Trial ...
Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Project Managers with a focus on Neuroscience or CNS to join our Clinical Trial ...
Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Project Managers with a focus on Neuroscience or CNS to join our Clinical Trial ...
Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Project Managers with a focus on Neuroscience or CNS to join our Clinical Trial ...
Clinical project implementation and management is required, Epic or Meditech specific experience is preferred. * Previous experience managing projects of small to medium scope and complexity. * Must ...
Clinical project implementation and management is required, Epic or Meditech specific experience is preferred. * Previous experience managing projects of small to medium scope and complexity. * Must ...
Clinical project implementation and management is required, Epic or Meditech specific experience is preferred. * Previous experience managing projects of small to medium scope and complexity. * Must ...
Clinical project implementation and management is required, Epic or Meditech specific experience is preferred. * Previous experience managing projects of small to medium scope and complexity. * Must ...
Clinical project implementation and management is required, Epic or Meditech specific experience is preferred. * Previous experience managing projects of small to medium scope and complexity. * Must ...
Clinical project implementation and management is required, Epic or Meditech specific experience is preferred. * Previous experience managing projects of small to medium scope and complexity. * Must ...
Project Manager Information Technology II - IM Project Management Office
Irving, TX · On-site
$94K - $111K/yr
Clinical project implementation and management is required, Epic or Meditech specific experience is preferred. * Previous experience managing projects of small to medium scope and complexity. * Must ...
Project Manager Information Technology II - IM Project Management Office
Irving, TX · On-site
$94K - $111K/yr
Clinical project implementation and management is required, Epic or Meditech specific experience is preferred. * Previous experience managing projects of small to medium scope and complexity. * Must ...
... manages the development of clinical evaluation plans and reports and interacts with various cross-functional teams in order to assist in strategy, plans, and project deliverables. Must be able to ...
... manages the development of clinical evaluation plans and reports and interacts with various cross-functional teams in order to assist in strategy, plans, and project deliverables. Must be able to ...
... manages the development of clinical evaluation plans and reports and interacts with various cross-functional teams in order to assist in strategy, plans, and project deliverables. Must be able to ...
... manages the development of clinical evaluation plans and reports and interacts with various cross-functional teams in order to assist in strategy, plans, and project deliverables. Must be able to ...
Registered Dietitian Clinical Research - PRN
Fort Worth, TX · On-site
$42/hr
Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner. * Regularly stay informed on the latest nutrition and ...
Registered Dietitian Clinical Research - PRN
Fort Worth, TX · On-site
$42/hr
Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner. * Regularly stay informed on the latest nutrition and ...
Registered Dietitian Clinical Research - PRN
Fort Worth, TX · Remote
$42/hr
Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner. * Regularly stay informed on the latest nutrition and ...
Registered Dietitian Clinical Research - PRN
Fort Worth, TX · Remote
$42/hr
Works cooperatively with Clinical Project Manager and site personnel to complete visits and submit accurate source documents in a timely manner. * Regularly stay informed on the latest nutrition and ...
... manages the development of clinical evaluation plans and reports and interacts with various cross-functional teams in order to assist in strategy, plans, and project deliverables. Must be able to ...
... manages the development of clinical evaluation plans and reports and interacts with various cross-functional teams in order to assist in strategy, plans, and project deliverables. Must be able to ...
Study Start-Up Project Manager
Irving, TX · On-site
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays a key ...
Study Start-Up Project Manager
Irving, TX · On-site
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays a key ...
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays a key ...
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays a key ...
The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities within metabolic trials.
The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities within metabolic trials.
Associate Clinical Trial Manager - PhD - Metabolic - Dallas, TX
Irving, TX · On-site
$31 - $42.50/hr
The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities within metabolic trials.
Associate Clinical Trial Manager - PhD - Metabolic - Dallas, TX
Irving, TX · On-site
$31 - $42.50/hr
The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities within metabolic trials.
Project Manager
Fort Worth, TX · On-site
$60K - $75K/yr
PRIMARY FUNCTION Manage the scope, schedule and budget for client projects. Act as main point of contact for internal project team, client team; and third-party product and service partners. Request ...
Project Manager
Fort Worth, TX · On-site
$60K - $75K/yr
PRIMARY FUNCTION Manage the scope, schedule and budget for client projects. Act as main point of contact for internal project team, client team; and third-party product and service partners. Request ...
Project Manager
Fort Worth, TX · On-site
$60K - $75K/yr
PRIMARY FUNCTION Manage the scope, schedule and budget for client projects. Act as main point of contact for internal project team, client team; and third-party product and service partners. Request ...
Quick apply
Project Manager
Fort Worth, TX · On-site
$60K - $75K/yr
PRIMARY FUNCTION Manage the scope, schedule and budget for client projects. Act as main point of contact for internal project team, client team; and third-party product and service partners. Request ...
Clinical Project Manager information
See Addison, TX salary details
$28.16 - $35.14
16% of jobs
$40.53 is the 25th percentile. Wages below this are outliers.
$35.14 - $42.12
12% of jobs
$42.12 - $49.10
14% of jobs
The median wage is $53.75 / hr.
$49.10 - $56.08
13% of jobs
$56.08 - $63.06
15% of jobs
$66.26 is the 75th percentile. Wages above this are outliers.
$63.06 - $70.04
13% of jobs
$70.04 - $77.03
4% of jobs
$77.03 - $84.01
5% of jobs
$84.01 - $90.99
5% of jobs
$90.99 - $97.97
1% of jobs
$97.97 - $104.95
2% of jobs
$28
$58
$104
How much do clinical project manager jobs pay per hour?
As of Jul 17, 2026, the average hourly pay for clinical project manager in Addison, TX is $58.76, according to ZipRecruiter salary data. Most workers in this role earn between $40.96 and $68.89 per hour, depending on experience, location, and employer.
What is the difference between Clinical Project Manager vs Clinical Research Associate?
| Aspect | Clinical Project Manager | Clinical Research Associate |
|---|---|---|
| Credentials | Typically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMP | Usually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common |
| Work Environment | Manages multiple clinical trials, oversees teams, and coordinates with sponsors and sites | Monitors clinical sites, ensures protocol compliance, and collects data |
| Employer & Industry Usage | Found in pharmaceutical, biotech, and CRO companies overseeing entire projects | Primarily employed by CROs and sponsors to monitor trial sites |
The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.
What Does a Clinical Project Manager Do?
A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.
What are the key skills and qualifications needed to thrive as a Clinical Project Manager, and why are they important?
To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.
What does a Clinical Project Manager do?
A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.
What are some common challenges Clinical Project Managers face when coordinating multi-site clinical trials?
Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.
More about Clinical Project Manager jobs
What are popular job titles related to Clinical Project Manager jobs in Addison, TX? For Clinical Project Manager jobs in Addison, TX, the most frequently searched job titles are:
What job categories do people searching Clinical Project Manager jobs in Addison, TX look for? The top searched job categories for Clinical Project Manager jobs in Addison, TX are:
What cities near Addison, TX are hiring for Clinical Project Manager jobs? Cities near Addison, TX with the most Clinical Project Manager job openings:
Job description
Company Description
SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services.
Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential.
Job Description
The Study Project Manager is ultimately accountable for the planning, execution, issue resolution, and communication / communication planning required for successful execution of each assigned clinical study or designated internal project.
This includes holding planning meetings as needed with test facility or other personnel regarding study/project design, contract, timeline for prestudy activities (such as schedule, protocol, ethics committee, recruiting, documents, and data management), study/project execution, data analysis and clinical study report/other deliverables, and archiving.
During study/project execution, the Study Project Manager tracks project activities against the schedule, orchestrates all functions to identify and remove roadblocks, anticipates and resolves issues, and coordinates the participation of external resources.
The Study Project Manager may conduct a post-mortem analysis. The Study Project Manager is the central point of communication to the study Sponsor or project requestor, and sends updates on a scheduled basis including information from all relevant functional areas
Qualifications
Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.
SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services.
Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential.
Job Description
The Study Project Manager is ultimately accountable for the planning, execution, issue resolution, and communication / communication planning required for successful execution of each assigned clinical study or designated internal project.
This includes holding planning meetings as needed with test facility or other personnel regarding study/project design, contract, timeline for prestudy activities (such as schedule, protocol, ethics committee, recruiting, documents, and data management), study/project execution, data analysis and clinical study report/other deliverables, and archiving.
During study/project execution, the Study Project Manager tracks project activities against the schedule, orchestrates all functions to identify and remove roadblocks, anticipates and resolves issues, and coordinates the participation of external resources.
The Study Project Manager may conduct a post-mortem analysis. The Study Project Manager is the central point of communication to the study Sponsor or project requestor, and sends updates on a scheduled basis including information from all relevant functional areas
- Establish a standard project dashboard to show standard phases each study may go through in addition to visual status, timeline, and risk information. This may include a version that can be shared with clients as a standard scheduled update.
- Establish a detailed project plan for each assigned study to coordinate and track execution with the appropriate functional teams.
- Run a weekly Project Management / Study Scheduling meeting to provide status updates, gather input for scheduling of new studies, escalate issues, and align on client communications / communication plans as needed
- Facilitate discussions for issue resolution by pulling together the needed experts and driving to consensus on the path forward, when required
- Communicate status or updates to project sponsors, or coordinate updates with the relevant Global Key Account Manager (GKAM)
- Suggest improvements to our study execution process based on observed inefficiencies or identified opportunities
- Complete training within required deadline
- Adhere to internal standards, policies, and procedures
Qualifications
- Bachelor's degree (science, business, or project management preferred)
- 6-18 months clinical research experience or equivalent
- 2+ years of project management experience
- Ability to learn and use MS Project or other project management platform
- Strong understanding of clinic processes and flow, and ability to create study schedules that make good use of resources
- Ability to work with others to communicate requirements, build consensus, and overcome problems
- Excellent ability to establish priorities with minimal supervision and attention to detail
Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.