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Clinical Operations Associate Jobs in Allen, TX (NOW HIRING)

The Senior Associate will leverage strong Epic clinical application expertise, healthcare operational knowledge, and project management discipline to help clients improve care delivery, provider ...

... operational processes and meets their goals daily. About us : Stanton Optical is among the nation ... An associate's degree or advanced certification beyond a high school diploma; or currently enrolled ...

... clinical services follow operational processes and meets their goals daily. About us : Stanton ... An associates degree or advanced certification beyond a high school diploma; or currently enrolled ...

... operational processes and meets their goals daily. About us : Stanton Optical is among the nation ... An associate's degree or advanced certification beyond a high school diploma; or currently enrolled ...

... operational processes and meets their goals daily. About us : Stanton Optical is among the nation ... An associate's degree or advanced certification beyond a high school diploma; or currently enrolled ...

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Clinical Operations Associate information

See Allen, TX salary details

$10

$24

$49

How much do clinical operations associate jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical operations associate in Allen, TX is $24.41, according to ZipRecruiter salary data. Most workers in this role earn between $16.54 and $28.17 per hour, depending on experience, location, and employer.

What is a clinical operations associate?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What are the typical responsibilities and team dynamics for a clinical operations associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

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

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

What are the most commonly searched types of Clinical Operations jobs in Allen, TX?

The most popular types of Clinical Operations jobs in Allen, TX are:

What are popular job titles related to Clinical Operations Associate jobs in Allen, TX?

For Clinical Operations Associate jobs in Allen, TX, the most frequently searched job titles are:

What job categories do people searching Clinical Operations Associate jobs in Allen, TX look for?

The top searched job categories for Clinical Operations Associate jobs in Allen, TX are:

What cities near Allen, TX are hiring for Clinical Operations Associate jobs?

Cities near Allen, TX with the most Clinical Operations Associate job openings:

Infographic showing various Clinical Operations Associate job openings in Allen, TX as of July 2026, with employment types broken down into 92% Full Time, and 8% Part Time. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $50,777 per year, or $24.4 per hour.

Clinical Trial Liaison CTL Ophthalmology NationwideUSBased

T.MAC

Dallas, TX โ€ข On-site

Other

Posted 22 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 Companyโ€™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 Companyโ€™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 driverโ€™s license

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

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