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Ctl Jobs in Texas (NOW HIRING)

Majestic Steel

Operator (CTL)

Houston, TX · On-site

$21/hr

Why Work With Us: * Pay: Starting rate is $21.00/ hour for Operator in Training; could be eligible for more based on experience * Hours: Monday - Friday, 4:00 AM - 12:30 PM, with overtime as required

Majestic Steel

Operator (CTL)

Houston, TX · On-site

$21/hr

Why Work With Us: * Pay: Starting rate is $21.00/ hour for Operator in Training; could be eligible for more based on experience; Eligible for a $2,500 onboarding bonus for Operator roles (subject to ...

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All JobsCtl JobsCtl Jobs in Texas

Ctl information

See Texas salary details

$59.2K

$126.8K

$184.5K

How much do ctl jobs pay per year?

As of Aug 21, 2026, the average yearly pay for ctl in Texas is $126,841.00, according to ZipRecruiter salary data. Most workers in this role earn between $105,700.00 and $151,900.00 per year, depending on experience, location, and employer.

What is a CTL?

A CTL (Controller) job typically involves overseeing financial reporting, budgeting, and compliance within an organization. Controllers manage accounting records, ensure regulatory adherence, and provide financial insights to support decision-making. They often supervise accounting teams and collaborate with executives to drive financial strategy.

What are the typical career advancement opportunities for a CTL engineer?

As a Ctl Engineer, you can advance to senior engineering positions, project management roles, or specialize further in automation, safety, or process optimization. Many professionals pursue additional certifications or a master's degree to move into engineering management or lead multi-disciplinary teams. The role often provides a strong foundation in cross-functional collaboration, which is valued in technical leadership. Advancement typically depends on demonstrated expertise, successful project outcomes, and ongoing professional development.

What are the key skills and qualifications needed to thrive in the CTL position, and why are they important?

To excel as a Control (Ctl) Engineer, a solid background in electrical engineering, process control, and automation systems is essential, often supported by a bachelor's degree in engineering. Familiarity with PLC/DCS programming, SCADA systems, and relevant safety certifications (such as ISA or TÜV) is typically required. Strong problem-solving abilities, communication skills, and attention to detail are distinguishing soft skills in this profession. These competencies ensure reliable system performance, safe operations, and effective teamwork in industrial environments.

What are popular job titles related to Ctl jobs in Texas?

For Ctl jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Ctl jobs in Texas look for?

The top searched job categories for Ctl jobs in Texas are:

What cities in Texas are hiring for Ctl jobs?

Cities in Texas with the most Ctl job openings:

Ctl jobs near you
Infographic showing various Ctl job openings in Texas as of August 2026, with employment types broken down into 84% Full Time, 10% Part Time, 4% Contract, and 2% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $126,841 per year, or $61 per hour.

Clinical Trial Liaison CTL Ophthalmology NationwideUSBased

T.MAC

Dallas, TX • On-site

Other

Posted 24 days ago

Job description

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’s Ophthalmology clinical trial pipeline. The CTL will serve as a clinical trial and clinical program subject matter expert and problem solver to help study sites optimize their study performance. The CTL will work full time to help sites address challenges in study delivery that could impact the Company’s study or program goals.

This role involves compliant collaboration with KOLs, investigators, research staff members and CRO to build strong professional partnerships, provide credible scientific expertise, and serve as a field-based extension of the clinical trial team to support ongoing studies.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Site and Investigator Partnerships

  • Create investigator engagement plans to support site-specific recruitment, site identification and/or selection
  • Provide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers, and clinical trial recruitment and retention
  • Generate feasible, time-bound, prioritized action plans to address any barriers identified at clinical sites, document the plan and meet with the sites regularly to measure progress
  • Serve as a liaison to internal R&D and Clinical Operations functions to ensure the effective support of PIs
  • Collection of key medical insights from PIs to inform refinement of strategies

Building Company & Pipeline Advocacy

Through compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnerships

Expertise Management and Cross Functional Support

  • Maintain awareness of and access to internal and external information sources available to support high-quality scientific exchanges with HCPs
  • Develop/increase knowledge of relevant medical literature and critical appraisal of scientific publications
  • Maintain knowledge base and scientific expertise on all assigned disease areas and products
  • Develop and update knowledge of applicable pharmaceutical guidelines and regulations. Code of Ethical Practices and company policies
  • Provide scientific input and participate in local medical and cross functional initiatives
  • Build scientific relationships with key thought leaders, healthcare professionals, investigators and their teams, government organizations, and patient and provider advocacy groups
  • Collect key strategic insights from top research KOLs and HCPs to support strategic initiatives
  • Maintain working knowledge of regulatory and ethical requirements for all initiatives.

QUALIFICATIONS:

  • Knows how clinical sites operate, and has a history of helping study sites solve practical problems on clinical trials
  • Healthcare/science background inclusive of PharmD, PhD and MD, OD (or equivalent) required.
  • Clinical background in the area of Ophthalmology, with expertise in retinal diseases required
  • 5+ years of clinical research or clinical research support experience within academic, healthcare system or industry setting (e.g., clinical research coordinator, research manager, clinical research associate, study coordinator, research director) is required. Qualified individuals will have a strong familiarity and experience with clinical research and study site logistics.
  • Frequent travel is required. Availability to travel up to 50% of time
  • Availability to attend meetings on holidays and weekends
  • Clean and valid driver’s license

Salary offers to be determined based on industry experience, education, and therapeutic expertise.

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