... clinical research experience, including 4 years of strong trial operations management experience across all study periods (start-up, maintenance and closure). Additional Information Regards Rahul ...
... clinical research experience, including 4 years of strong trial operations management experience across all study periods (start-up, maintenance and closure). Additional Information Regards Rahul ...
The candidate will act as the Clinical Trial Manager in the implementation of Investigator Sponsored Trials primarily in Diabetes, but may include other therapeutic areas. Key responsibilities will ...
The candidate will act as the Clinical Trial Manager in the implementation of Investigator Sponsored Trials primarily in Diabetes, but may include other therapeutic areas. Key responsibilities will ...
Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH-GCP and ...
Quick apply
Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH-GCP and ...
Manage clinical trial operations from startup through closeout Oversee adverse event reporting and pharmacovigilance systems Ensure compliance with ICH-GCP and regulatory requirements Coordinate DSMB ...
Manage clinical trial operations from startup through closeout Oversee adverse event reporting and pharmacovigilance systems Ensure compliance with ICH-GCP and regulatory requirements Coordinate DSMB ...
The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical Supplies strategies and processes in order to achieve clinical study objectives in assigned ...
The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical Supplies strategies and processes in order to achieve clinical study objectives in assigned ...
Venesco is seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical trial operations and ensure robust safety surveillance practices. Requirements Key Responsibilities ...
Venesco is seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical trial operations and ensure robust safety surveillance practices. Requirements Key Responsibilities ...
The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical Supplies strategies and processes in order to achieve clinical study objectives in assigned ...
The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical Supplies strategies and processes in order to achieve clinical study objectives in assigned ...
Local Operations Manager - Advanced - Immunology ICON is a global healthcare intelligence and ... As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ...
New
Local Operations Manager - Advanced - Immunology ICON is a global healthcare intelligence and ... As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ...
New
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Quick apply
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Clinical Trial Manager
Ridgefield, CT · On-site
Duties As clinical trial manager (CTM), accountable for the operational management of the local component of a clinical trial. Level of oversight assures achievement of trial recruitment commitment ...
Clinical Trial Manager
Ridgefield, CT · On-site
Duties As clinical trial manager (CTM), accountable for the operational management of the local component of a clinical trial. Level of oversight assures achievement of trial recruitment commitment ...
Role Overview The Sr. Manager, Clinical Trial Operations Planning & Analytics is responsible for the strategic planning and analytics capability to support current and future Legend pipeline studies.
Role Overview The Sr. Manager, Clinical Trial Operations Planning & Analytics is responsible for the strategic planning and analytics capability to support current and future Legend pipeline studies.
Clinical Trial Manager
San Diego, CA · Remote
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Clinical Trial Manager
San Diego, CA · Remote
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Legend Biotech is seeking a Sr. Manager, Clinical Trial Operations Planning & Analytics as part of the Clinical Operations team based in Somerset , NJ . Role Overview The Sr. Manager, Clinical Trial ...
Legend Biotech is seeking a Sr. Manager, Clinical Trial Operations Planning & Analytics as part of the Clinical Operations team based in Somerset , NJ . Role Overview The Sr. Manager, Clinical Trial ...
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Quick apply
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Legend Biotech is seeking a Sr. Manager, Clinical Trial Operations Planning & Analytics as part of the Clinical Operations team based in Somerset, NJ.Role OverviewThe Sr. Manager, Clinical Trial ...
Legend Biotech is seeking a Sr. Manager, Clinical Trial Operations Planning & Analytics as part of the Clinical Operations team based in Somerset, NJ.Role OverviewThe Sr. Manager, Clinical Trial ...
The Manager, Trial Operations is a senior operations role within the Trial Operations team, reporting directly to the Director of Trial Operations. The Manager owns three interconnected workstreams ...
The Manager, Trial Operations is a senior operations role within the Trial Operations team, reporting directly to the Director of Trial Operations. The Manager owns three interconnected workstreams ...
Local Operations Manager - Advanced - Cross TA ICON is a global healthcare intelligence and ... As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ...
Local Operations Manager - Advanced - Cross TA ICON is a global healthcare intelligence and ... As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ...
Clinical Trial Operations Manager information
See salary details
$28.85 - $34.97
4% of jobs
$34.97 - $41.08
6% of jobs
$41.08 - $47.20
7% of jobs
$51.79 is the 25th percentile. Wages below this are outliers.
$47.20 - $53.32
9% of jobs
$53.32 - $59.44
15% of jobs
The median wage is $62.14 / hr.
$59.44 - $65.56
18% of jobs
$69.92 is the 75th percentile. Wages above this are outliers.
$65.56 - $71.68
21% of jobs
$71.68 - $77.80
7% of jobs
$77.80 - $83.92
6% of jobs
$83.92 - $90.03
3% of jobs
$90.03 - $96.15
2% of jobs
$28
$62
$96
How much do clinical trial operations manager jobs pay per hour?
As of Jun 11, 2026, the average hourly pay for clinical trial operations manager in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.
What are some common challenges faced by Clinical Trial Operations Managers, and how can they be addressed?
Clinical Trial Operations Managers often encounter challenges such as ensuring regulatory compliance across multiple sites, managing tight timelines, and coordinating diverse teams. Effective communication and proactive planning are essential to address these difficulties. Leveraging project management tools and fostering strong relationships with investigators and site staff can also help streamline operations and reduce risks of delays or protocol deviations.
What is the difference between Clinical Trial Operations Manager vs Clinical Research Coordinator?
| Aspect | Clinical Trial Operations Manager | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree; often advanced degrees or certifications in clinical research or management | Bachelor's degree in health sciences or related field; certifications like CCRP are common |
| Work Environment | Oversees multiple trials, manages teams, and coordinates with stakeholders in clinical settings | Works directly with participants, manages trial documentation, and supports daily trial activities |
| Employer & Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, clinics, research institutions |
The Clinical Trial Operations Manager focuses on overseeing entire clinical trial processes, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at the trial site, working closely with participants and supporting trial documentation. Both roles require relevant certifications and are essential in the clinical research industry, but they differ in scope and responsibilities.
What are the key skills and qualifications needed to thrive as a Clinical Trial Operations Manager, and why are they important?
To thrive as a Clinical Trial Operations Manager, you need a strong background in clinical research, regulatory compliance, project management, and a relevant degree such as in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are highly valued. Leadership, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These competencies ensure clinical trials are conducted efficiently, ethically, and in accordance with regulatory requirements.
What does a Clinical Trial Operations Manager do?
A Clinical Trial Operations Manager oversees the planning, execution, and completion of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate with cross-functional teams, manage budgets and timelines, and handle any issues that arise during the trial process. This role is crucial for ensuring that new drugs or medical devices are tested safely and effectively before reaching the market.
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What are the most commonly searched types of Clinical Trial Operations jobs? The most popular types of Clinical Trial Operations jobs are:
What states have the most Clinical Trial Operations Manager jobs? States with the most job openings for Clinical Trial Operations Manager jobs include:
What job categories do people searching Clinical Trial Operations Manager jobs look for? The top searched job categories for Clinical Trial Operations Manager jobs are:
Job description
Company Description
Saviance Technologies is a global provider of Enterprise Technology
Solutions for the US Healthcare Sector focusing on the latest technology
SMAC stack (Social, Mobility, Analytics and Cloud). We provide
innovative solutions and enable meaningful Use of IT by designing
patient care & community portals, collaboration applications, big
data insights for wellness & population health, ICD-10 resources and
process automation.
Our clients are distinguished hospitals, healthcare
institutions and manufacturers of consumer healthcare products. Saviance
has enabled them to achieve critical objectives such as increased
projects visibility across the organization, improved knowledge
management, enhanced technological prowess, improved productivity,
better return on investment and therefore the ability to make
value-added business decisions.
Job Description
The CTOM is responsible for the overall operational planning and activities for the implementation and conduct of studies (clinical trials, observational studies, compassionate use and registries) including oversight of data management activities in compliance with GCPs, SOPs and standards within established timelines and budgets.
The CTOM is involved in the scientific conduct of the study and acts as the leader of operational disciplines to guarantee release of homogeneous high quality data, in close collaboration with other functions (e.g. Medical Operations, Monitoring Team, Biostatistics) and with the CRO, for outsourced trials.
Capable of interacting effectively with scientists, support functions, subject matter experts and managers within and outside department; serve as internal consultant on assigned area and liaise with external organizations on projects.
- Strong interpersonal and communication/presentation skills (verbal and written);
- Ability to handle multiple tasks and to prioritize, strong organizational skills
- Leadership & Project Management abilities: ability to conduct effective and efficient international team meetings (Clinical Trial Team, expert meeting, etc), demonstrate good collaboration skills, have a positive, “can do” attitude, be proactive
- Capability to perform effective vendor and stakeholder management including budget management, active and effectual oversight of CROs
- Possess a solid understanding of data management activities (eCRF development from protocol design, database concepts, data flow, data cleaning, etc.)
- Decision-making and problem-solving skills
- Ability to work autonomously and to efficiently & effectively provide status reports
- Ability to anticipate, identify and timely escalate issues and to define appropriate action plans
- Ability to anticipate, identify and mitigate risks, including their likelihood, scope and impact and to develop CAPAs
- Good cross-functional team leader who fosters team spirit and team motivation (team work)
- Knowledge and qualification with international standards (e.g. GCP, CDISC, etc.), company tools (including data management systems), processes and SOPs
- Ability to work in an international environment with internal and/or external partners (CROs etc)
- Strong English skills (verbal and written if English is the second language)
- Competence to adapt and be flexible to change and managing internal and external impediments
- Ability to “think outside of the box” and make adjustments/create action plans to meet timelines.
- Prior experience with pediatric studies preferred
- Able to work on site at least 3 days per week
Qualifications
10 years of experience in pharmaceutical industry or clinical-related discipline including at least 7 years clinical research experience, including 4 years of strong trial operations management experience across all study periods (start-up, maintenance and closure).
Additional Information
Regards
Rahul Kumar
732-593-8302
About Saviance
Sourced by ZipRecruiter
Saviance is a modern consulting firm providing a variety of professional services to its clients in the US. We bring twenty three years of experience to the table. Our consultants are qualified experts and extremely talented. We understand the business behind the technology, and work with many of the top Fortune 100 companies and provide innovative, scalable, robust and secure solutions. At the forefront of the Staffing and IT Solutions industry, Saviance is certified by NMSDC as a Tier 1, Minority Business Enterprise (MBE) . We are a self- certified Small Business and self- certified Woman Owned Business committed to maximizing global workforce solutions on behalf of our clients, empowering businesses and talent through applied human intelligence. We are a Diversity Supplier with global reach specializing in a business services blend of talent, technology, and a relentless commitment to customer success. It’s our diversity that’s acts as a core component of our culture, our approach to business, and the opportunities we provide to our clients and our employees.
Industry
It services
Company size
201 - 500 Employees
Headquarters location
East Rutherford, NJ, US
Year founded
1999