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Clinical Science Manager Jobs in Texas (NOW HIRING)

Agilent

Clinical Affairs Scientist

Houston, TX · On-site +1

$105K - $197K/yr

This position reports to the Manager of Clinical Affairs Sciences and has no direct reports. Responsibilities include but are not limited to: * Provide thought leadership on key relevant clinical ...

Neuralink

Clinical Scientist

Austin, TX · On-site

As a Clinical Scientist I, you will support the development, design, and execution of Neuralink ... High attention to detail and ability to manage multiple priorities Preferred Qualifications:

Latent AI

Clinical Scientist

Austin, TX · On-site

$108 - $200/hr

As a Clinical Scientist I, you will support the development, design, and execution of Neuralink ... High attention to detail and ability to manage multiple priorities Preferred Qualifications:

Neuralink

Clinical Scientist

Austin, TX · On-site

As a Clinical Scientist I, you will support the development, design, and execution of Neuralink ... High attention to detail and ability to manage multiple priorities Preferred Qualifications:

Icon plc

Senior Clinical Scientist

Dallas, TX

Senior Clinical Scientist (Hematology-Oncology) ICON is a global healthcare intelligence and ... Ability to work independently, manage multiple priorities, and thrive in a dynamic environment

DiaSorin

Clinical Data Scientist

Austin, TX

Obsessed by Science. Entrepreneurial by Nature. United by Purpose. Diasorin is a global leader in ... Manage the development of primary and validation programming and lead the report generation ...

DiaSorin

Clinical Data Scientist

Austin, TX · On-site

Obsessed by Science. Entrepreneurial by Nature. United by Purpose. Diasorin is a global leader in ... Manage the development of primary and validation programming and lead the report generation ...

Medix

Clinical Research Manager

Dallas, TX · On-site

$48.08 - $52.88/hr

Manages daily clinical research operations and standard operating procedures. * Develops project ... As a job position within our Clinical Sciences division, a successful completion of a background ...

IQVIA

Medical Science Liaison

Dallas, TX

You will be asked to contribute clinical insight to inform decision making on various aligned teams ... Proficiency with CRM systems and standard collaboration tools, including Microsoft Teams ...

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Clinical Science Manager information

See Texas salary details

$40.5K

$76.7K

$130.4K

How much do clinical science manager jobs pay per year?

As of Sep 6, 2026, the average yearly pay for clinical science manager in Texas is $76,722.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,600.00 and $83,400.00 per year, depending on experience, location, and employer.

What is a clinical science manager?

Clinical Science Managers are professionals who oversee and coordinate clinical research projects, often within the pharmaceutical, biotechnology, or medical device industries. They are responsible for managing clinical trials, ensuring regulatory compliance, and collaborating with cross-functional teams such as clinical operations, regulatory affairs, and medical affairs. Their role involves protocol development, data analysis, and ensuring the safety and efficacy of investigational products. Clinical Science Managers also play a critical part in interpreting study results and presenting findings to stakeholders. They typically have advanced degrees in life sciences and significant experience in clinical research.

What are the key skills and qualifications needed to thrive as a clinical science manager?

To thrive as a Clinical Science Manager, you need a solid background in clinical research, life sciences, and project management, typically supported by an advanced degree (e.g., PharmD, PhD, or MD) and industry experience. Familiarity with clinical trial management systems, regulatory compliance tools, and data analysis platforms is crucial. Strong leadership, strategic thinking, and effective communication skills help you manage cross-functional teams and build relationships with stakeholders. These competencies ensure the successful design, execution, and oversight of clinical studies, ultimately advancing scientific and business goals.

How does a clinical science manager typically collaborate with cross-functional teams during clinical trial development?

Clinical Science Managers play a key role in bridging scientific objectives with operational execution by working closely with clinical operations, regulatory affairs, data management, and medical affairs teams. They often lead the development of clinical protocols and ensure scientific integrity throughout the study, facilitating regular meetings and communication to align project goals and timelines. Their collaborative efforts help anticipate and resolve challenges, streamline processes, and ensure that trials meet regulatory requirements and scientific standards.

What is the difference between Clinical Science Manager vs Clinical Research Associate?

AspectClinical Science ManagerClinical Research Associate
CredentialsTypically requires advanced degrees (e.g., Master’s or PhD) and industry experienceUsually holds a bachelor’s degree in life sciences or related field
Work EnvironmentLeads teams, manages projects, and oversees clinical studiesMonitors clinical trials at sites, ensures protocol compliance
Employer & Industry UsagePharmaceutical, biotech, and medical device companiesContract research organizations, pharmaceutical companies
Search & Comparison IntentUnderstanding managerial roles in clinical scienceFocus on trial monitoring and site management

The Clinical Science Manager typically oversees clinical projects and manages teams, requiring advanced credentials. In contrast, the Clinical Research Associate focuses on monitoring clinical trials at sites. Both roles are essential in the clinical research process but differ in responsibilities and experience levels.

What are popular job titles related to Clinical Science Manager jobs in Texas?

For Clinical Science Manager jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Clinical Science Manager jobs in Texas look for?

The top searched job categories for Clinical Science Manager jobs in Texas are:

What cities in Texas are hiring for Clinical Science Manager jobs?

Cities in Texas with the most Clinical Science Manager job openings:

Clinical Science Manager jobs near you

Clinical Affairs Scientist

Agilent

Houston, TX • On-site, Remote

$105K - $197K/yr

Full-time

Posted 17 days ago

Key responsibilities

  • Support clinical trial study designs and execution, including authoring study protocols and reports.

  • Collaborate with cross-functional teams and external partners to generate clinical evidence and ensure compliance.

  • Provide scientific oversight and contribute to regulatory submissions, scientific publications, and presentations.

Agilent Technologies rating

8.5

Company rating: 8.5 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers

Job description

Job Description

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer(OCMO) Global Clinical Affairs team. The CAS' main responsibilities will be to support clinical evidence generation, in conjunction with cross-functional teams as part of the co-development process of companion diagnostics in the field of oncology. This position will support clinical trial study designs and execution, regulatory applications, and scientific marketing deliverables. The ideal candidate will have a strong background in clinical science/research and experience working in pharmaceutical, biomarker, and/or in vitro diagnostic clinical development. The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements. This position reports to the Manager of Clinical Affairs Sciences and has no direct reports.
Responsibilities include but are not limited to:

  • Provide thought leadership on key relevant clinical topics to support strategy development and execution.

  • Generation of content to support external validation studies including study design and authoring of study protocols and reports. May also contribute to cutoff/cutpoint determination studies, method comparison, bridging, and analytical concordance studies.

  • Design and develop databases, Electronic Data Capture (EDC) systems, and case report forms.

  • Contribute to risk analyses, study quality control activities, and instream data monitoring in clinical trials.

  • Ensure scientific validity of reported results including statistical analysis, tabulation, and presentation of data.

  • Collaborate with regulatory and development teams during the submission process including authoring of clinical performance information and other documentation such as Instructions for Use (IFU).

  • Provide clinical and scientific oversight of local marketing and commercial materials.

  • Ensure effective, efficient and compliant Clinical Affairs processes including preparing, revising, and maintaining standard operating procedures for the conduct of clinical studies.

  • Serve as the clinical science subject matter expert in cross-functional internal meetings as well as meetings with pharmaceutical partners and regulatory bodies.

  • Author manuscripts, abstracts, whitepapers and prepare oral/poster presentations.

  • Support audits and inspections as a clinical subject matter expert.

Qualifications

  • Master's degree or advanced degree (e.g., Ph.D., Pharm. D., M.D.) in pharmaceutical, medical or relevant biomedical science fields. Advanced Degree preferred.

  • 4+ years of experience in IVD product development, clinical research, medical writing, and/or clinical science in the medical device and/or pharmaceutical industry.

  • Familiarity with clinical trial design, conduct, and oversight including biostatistics, and Good Clinical Practice preferred.

  • Ability to interpret regulatory standards, guidance, and laws.

  • Strong scientific, medical writing, and presentation skills

  • Exceptional ability to manage multiple projects in a fast-paced environment with changing priorities.

  • Must be able to work and make independent decisions, understand complex scientific and clinical data information, and be able to take the initiative to lead projects and assignments.

  • Experience working with external partners and/or regulatory bodies including the FDA.

  • Knowledge in oncology, immunology, and/or pathology preferred.

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least August 27, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $105,280.00 - $197,400.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: NoShift: DayDuration: No End DateJob Function: Medical/Clinical

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