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Director Remote Clinical Informatics Jobs in Rowlett, TX

MaxHealth DPC

Remote Psychiatrist

Dallas, TX · Remote

... Direct Primary Care, Personal Injury, Mental Health, Brain Health, and Longevity Medicine. Our ... Support quality improvement initiatives and clinical best practices. Qualifications Required

Career Search

Director, Revenue Cycle

Mckinney, TX · Remote

All Central Region Service Lines Remote The Director, Revenue Cycle - Central Region is a senior ... The Director will partner closely with Finance, Operations, Clinical Leadership, Compliance, IT ...

pharma& US Inc

Director, National Access

Addison, TX · Remote

*This is a remote position* Job Summary The Director, National Access will play a critical role in ... and clinical pathway implementation. * Prior experience negotiating PBM contracts preferred.

Tuesday Health

Clinical Supervisor (Texas)

Dallas, TX · Remote

Remote (must be located in Texas), Travel required up to 30% Who We Are: Tuesday Health is a value ... Provide direct supervision, coaching, and performance oversight to field-based clinical staff ...

pharma& US Inc

Director, National Access

Addison, TX · Remote

*This is a remote position* Job Summary The Director, National Access will play a critical role in ... and clinical pathway implementation. * Prior experience negotiating PBM contracts preferred.

Cleerly

Director, Corporate Accounts

Dallas, TX · On-site +1

... clinical trials to identify important findings beyond symptoms that increase a person's risk of ... While we are mostly a remote company, travel is required for some team meetings and cross function ...

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Director Remote Clinical Informatics information

See Rowlett, TX salary details

$35

$62

$94

How much do director remote clinical informatics jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for director remote clinical informatics in Rowlett, TX is $62.21, according to ZipRecruiter salary data. Most workers in this role earn between $47.02 and $77.84 per hour, depending on experience, location, and employer.

What does a director remote clinical informatics do?

A Director of Remote Clinical Informatics oversees the integration and management of clinical information systems, particularly for remote or telehealth environments. They ensure that healthcare technologies effectively support patient care, data management, and regulatory compliance. This role involves collaborating with clinical and IT teams to optimize workflows, implement new technologies, and maintain data security standards. Directors in this field also analyze data to improve healthcare outcomes and support decision-making processes across remote care settings.

What are the key skills and qualifications needed to thrive as a director remote clinical informatics?

To thrive as a Director of Remote Clinical Informatics, you need expertise in healthcare informatics, clinical workflows, and data analytics, typically supported by a relevant degree (such as nursing or health informatics) and managerial experience. Familiarity with electronic health record (EHR) systems, interoperability standards, data security protocols, and certifications like CPHIMS or RHIA are highly valuable. Strategic leadership, strong communication, and change management skills distinguish top performers in this role. These competencies are critical for successfully guiding remote teams, optimizing clinical processes, and ensuring effective technology adoption in healthcare organizations.

What are some common challenges faced by a director remote clinical informatics when managing geographically dispersed teams?

A Director of Remote Clinical Informatics often encounters challenges related to communication, coordination, and maintaining consistent standards across teams in different locations. Ensuring that all team members stay aligned with organizational goals and regulatory requirements can be complex, especially when dealing with varying local practices and time zones. To address these challenges, directors typically implement robust virtual collaboration tools, set clear expectations, and foster a culture of transparency. Regular virtual meetings and effective training programs help maintain cohesion and high performance within the remote team.

What is the difference between Director Remote Clinical Informatics vs Clinical Informatics Manager?

AspectDirector Remote Clinical InformaticsClinical Informatics Manager
ResponsibilitiesOversees clinical informatics strategies, leads teams, and aligns technology with organizational goals.Manages daily clinical informatics operations, supports implementation, and ensures system functionality.
Required CredentialsTypically requires a clinical background, informatics certification, and leadership experience.Often requires clinical experience and informatics knowledge, with some certifications preferred.
Work EnvironmentRemote or hybrid, working with executive teams and cross-departmental staff.Primarily on-site or hybrid, collaborating closely with clinical staff and IT teams.

The main difference lies in scope and leadership level. The Director Remote Clinical Informatics focuses on strategic planning and leadership, while the Clinical Informatics Manager handles daily operations and implementation support. Both roles require clinical and informatics credentials, but the director position involves broader organizational responsibilities.

What cities near Rowlett, TX are hiring for Director Remote Clinical Informatics jobs?

Cities near Rowlett, TX with the most Director Remote Clinical Informatics job openings:

Director Remote Clinical Informatics jobs near you

Clinical Trial Liaison (CTL), Ophthalmology (Nationwide/US-Based)

TMAC

Dallas, TX • Remote

Full-time

Re-posted 7 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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