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Clinical Operation Manager Jobs in Spring, TX (NOW HIRING)

S. Clinical Operations team. The CTM will oversee site management, monitoring oversight, and clinical trial operations activities to ensure compliance with GCP, regulatory requirements, and company ...

S. Clinical Operations team. The CTM will oversee site management, monitoring oversight, and clinical trial operations activities to ensure compliance with GCP, regulatory requirements, and company ...

Clinical Trial Manager

Houston, TX ยท On-site

$130K - $150K/yr

S. Clinical Operations team. The CTM will oversee site management, monitoring oversight, and clinical trial operations activities to ensure compliance with GCP, regulatory requirements, and company ...

Clinical Trial Manager

Houston, TX ยท On-site

$130K - $150K/yr

S. Clinical Operations team. The CTM will oversee site management, monitoring oversight, and clinical trial operations activities to ensure compliance with GCP, regulatory requirements, and company ...

Center Clinical Manager

Houston, TX ยท On-site

$59K - $82K/yr

In partnership with Dyad leaders, manages the center's clinical operations to ensure organizational objectives relative to SSP metrics, growth and strategy, membership goals are regularly met and/or ...

The Clinical Study Manager is an integral part of the Clinical Operations Team which manages planned and ongoing clinical studies. The Clinical Study Manager is responsible for overseeing the ...

The Clinical Study Manager is an integral part of the Clinical Operations Team which manages planned and ongoing clinical studies. The Clinical Study Manager is responsible for overseeing the ...

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Clinical Operation Manager information

See Spring, TX salary details

$31.1K

$87.2K

$166K

How much do clinical operation manager jobs pay per year?

As of Jul 30, 2026, the average yearly pay for clinical operation manager in Spring, TX is $87,244.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,500.00 and $101,000.00 per year, depending on experience, location, and employer.

What are some common challenges Clinical Operation Managers face when coordinating multi-site clinical trials?

Clinical Operation Managers often encounter challenges such as ensuring consistent protocol adherence across all sites, managing communication among geographically dispersed teams, and maintaining timelines despite unexpected delays. They must also address regulatory differences between sites and troubleshoot issues related to patient recruitment and data collection. Success in this role requires strong organizational skills, adaptability, and effective collaboration with investigators, coordinators, and regulatory personnel.

What are the key skills and qualifications needed to thrive as a Clinical Operation Manager, and why are they important?

To thrive as a Clinical Operation Manager, you need expertise in clinical project management, regulatory compliance, and a background in healthcare or life sciences, often supported by a relevant degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as PMP or Six Sigma are commonly required. Strong leadership, problem-solving abilities, and excellent communication skills set top performers apart in this role. These competencies are essential for ensuring efficient clinical operations, maintaining regulatory standards, and leading teams to deliver successful trial outcomes.

What are Clinical Operation Managers?

Clinical Operation Managers are professionals responsible for overseeing the daily operations of clinical research sites, medical facilities, or departments. They ensure that clinical trials or healthcare services are conducted efficiently, comply with regulations, and meet quality standards. Their duties often include supervising staff, managing budgets, implementing policies, and coordinating between various teams. Clinical Operation Managers play a crucial role in ensuring that patient care and research activities run smoothly and effectively.

What is the difference between Clinical Operation Manager vs Clinical Research Coordinator?

AspectClinical Operation ManagerClinical Research Coordinator
CredentialsBachelor's degree in health sciences, life sciences, or related field; often with project management certificationsBachelor's degree in health sciences, nursing, or related field; often with research-specific training
Work EnvironmentOversees multiple clinical trials, manages teams, and ensures compliance at a departmental levelCoordinates daily activities of clinical trials, interacts directly with participants and investigators
Employer & IndustryPharmaceutical companies, biotech firms, hospitals, research institutionsResearch sites, hospitals, academic institutions, contract research organizations

The Clinical Operation Manager focuses on overseeing clinical trial operations, managing teams, and ensuring compliance across projects. In contrast, the Clinical Research Coordinator handles the day-to-day activities of specific trials, working closely with participants and investigators. Both roles require relevant healthcare or science credentials, but their scope and responsibilities differ significantly.

What are popular job titles related to Clinical Operation Manager jobs in Spring, TX? For Clinical Operation Manager jobs in Spring, TX, the most frequently searched job titles are:
What cities near Spring, TX are hiring for Clinical Operation Manager jobs? Cities near Spring, TX with the most Clinical Operation Manager job openings:
Infographic showing various Clinical Operation Manager job openings in Spring, TX as of July 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 88% In-person, 4% Hybrid, and 8% Remote job distribution, with an average salary of $87,244 per year, or $41.9 per hour.

Clinical Operations Manager

ALLIANCE CLINICAL LLC

Houston, TX โ€ข On-site

$90K - $120K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago


Job description

About the Role:

The Clinical Operations Manager is responsible for daily clinic operations, administrative functions, and the management of office personnel. This role acts as a liaison between patients, medical staff, clinic staff, and management to ensure optimal clinic functioning. Additionally, the Manager plays an essential role in ensuring policies and procedures are followed, interpreting and communicating regulatory and protocol requirements, and ensuring that the clinic delivers exceptional patient care and functions efficiently.

Duties and Responsibilities:

  • Manage and train clinic site personnel.
  • Identify and implement strategies to expand the research capabilities at the site in alignment with the overall site business plan.
  • Oversee the implementation and maintenance of ACN quality standards at the site, including reading, analyzing, and interpreting regulations, protocols, and procedures to ensure studies are conducted in accordance with ICH GCPs.
  • Manage site budgets and expenses, including the analysis of figures, study costs, and other financial and operational data.
  • Work with the Medical Director/PI to address any study and/or clinical quality-related matters.
  • Ensure timely and appropriate communication with Sponsors and IRBs as necessary.
  • Develop site staffing plans to ensure the successful and efficient conduct of research studies. Identify and fulfill any site resource needs that are necessary to successfully conduct and/or recruit research studies.
  • Oversee the development of the patient recruitment plan and patient outreach process. Make ongoing adjustments/modifications to recruitment strategies based on the timely review of results to ensure financial and study-specific targets. Closely collaborate with any external vendors to facilitate successful patient enrollment strategies.
  • Read, comprehend, and communicate study protocols.
  • Oversee SIV, PSDV, and IMV.
  • Manage and facilitate study startup documentation, training, supplies, and timelines of study protocols.
  • Develop and implement operational plans, timelines, and budgets for clinical trials.
  • Share best practices with other ACN site locations with the goal of raising the overall level of operational competencies at ACN.
  • Monitor study progress, resolve data issues, and prepare status reports for leadership.
  • Work closely with CROs, CRAs, and IRBs.
  • Maintain site regulatory files.
  • Document temperatures for IP stored on-site.
  • Audit study e-source documentation to comply with study protocols.
  • Support audits and inspections.
  • Monitor study metrics and key performance indicators (KPIs).
  • Perform other duties as assigned.

Qualifications:

  • Bachelorโ€™s degree preferred in healthcare or equivalent clinical research experience.
  • Minimum of 5 years of clinical management experience or equivalent applicable experience in the clinical research industry.
  • Minimum of 3 years of experience working as a Clinical Research Coordinator required.
  • Comprehensive knowledge of FDA, GCP, and confidentiality.
  • Proven success in managing teams and working in direct patient care required.
  • Proficient problem-solving skills and conflict resolution.
  • Proficient in Microsoft Word, Excel, and PDF.
  • Excellent verbal and written communication skills.
  • A proven ability to constantly prioritize multiple projects in a rapidly changing environment.
  • Must be comfortable with a rapid-growth company.
  • Monitor project timelines and ensure milestones are met.

ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, Hโ€‘1B, TN, or STEM OPT training plans) are not eligible for this role.

Certificates, Licenses, and Registrations:

  • CPR certification.
  • Certified as a Medical Assistant or in Phlebotomy.
  • IATA and GCP certifications.

Benefits: Medical, Dental, Vision, 401k, PTO and more!

Location: Monday โ€“ Friday / on-site / Houston, TX

About the Company:

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.