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Clinical Science Manager Jobs in Texas (NOW HIRING)

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Clinical Science Manager information

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

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

Medical Affairs & Scientific Engagement Manager

Artidis

Houston, TX • On-site, Remote

Full-time

Re-posted 14 days ago


Job description

About Artidis

Artidis is a pioneering clinical stage health technology company that aims to set the gold standard in tissue analysis and therapy optimization. By combining its nanotechnology platform for rapid tissue analysis with a holistic data solution, Artidis accelerates drug discovery, tissue engineering, and personalized treatment. Artidis focuses its research and development efforts on solid tumors to enhance responses to chemo, immuno, and cell therapies, driving precision in cancer care.

Job Purpose

AsMedical Affairs & Scientific Engagement Manager, you will play a key role in building Artidis' scientific presence and supporting clinical adoption in the United States healthcare market.

You will develop and maintain strong relationships with clinicians, researchers, healthcare institutions, and key opinion leaders while leading scientific engagement activities, supporting evidence generation, and representing Artidis at major medical and scientific conferences.

Working closely with the Houston team and Basel headquarters, you will serve as a bridge between Artidis' Scientific, Clinical, Commercial, and Marketing teams, translating our innovative cancer diagnostics technology into meaningful clinical conversations.

This role requires a scientifically trained professional who can communicate complex scientific concepts clearly, build trusted relationships with healthcare leaders, and operate effectively in an international, fast-paced health technology environment.

Duties and Responsibilities

Medical Affairs & Scientific Engagement

  • Lead and execute Medical Affairs activities supporting Artidis' clinical and commercial growth in the United States.
  • Build and maintain relationships with clinicians, oncologists, researchers, hospitals, academic medical centers, and key opinion leaders.
  • Develop trusted scientific partnerships with healthcare professionals and external scientific collaborators.
  • Support clinical adoption by understanding healthcare workflows, clinical needs, and implementation challenges.
  • Provide scientific exchange and education to healthcare professionals.
  • Capture insights from physicians and healthcare stakeholders to support internal decision-making.

Scientific Evidence & Publications

  • Support publication activities, including manuscripts, abstracts, posters, presentations, and scientific congress submissions.
  • Collaborate with internal scientific teams, clinical investigators, and external research partners.
  • Develop scientific materials, presentations, briefing documents, and educational content.
  • Ensure scientific accuracy and consistency of Medical Affairs materials.

Medical Conferences & Scientific Events

  • Lead and support Artidis' scientific engagement activities at major medical conferences, including AACR, ASCO, ASTRO, SABCS, and other relevant oncology and diagnostics meetings.
  • Support conference strategy, scientific objectives, and engagement plans.
  • Coordinate KOL meetings, advisory boards, scientific discussions, and healthcare professional interactions.
  • Support abstract submissions, posters, presentations, and scientific communications.
  • Collaborate with Commercial, Marketing, and Operations teams on conference logistics, vendors, budgets, travel coordination, and on-site execution.
  • Track conference outcomes, stakeholder interactions, insights, and follow-up activities.

Cross-functional Collaboration

  • Work closely with Clinical, Scientific, Commercial, Marketing, Regulatory, and Basel HQ teams.
  • Represent ARTIDIS professionally at scientific meetings, advisory boards, conferences, and healthcare events.
  • Support the development of Artidis' Medical Affairs presence and strategy in the US market.

Qualifications

  • Master's degree or PhD in Life Sciences, Biomedical Sciences, Oncology, Medicine, Biotechnology, Diagnostics, or a related scientific discipline.
  • 5+ years of experience in Medical Affairs, Scientific Affairs, Clinical Affairs, KOL engagement, or related roles within biotechnology, MedTech, diagnostics, pharmaceutical, or healthcare organizations.
  • Experience working with clinicians, researchers, hospitals, academic medical centers, and healthcare professionals.
  • Experience supporting scientific publications, manuscripts, abstracts, posters, and presentations.
  • Strong understanding of oncology, diagnostics, precision medicine, or clinical workflows.
  • Experience with medical conferences, advisory boards, and scientific engagement activities.
  • Strong communication, presentation, and stakeholder management skills.
  • Ability to communicate complex scientific concepts to different audiences.
  • Strong project management skills with the ability to manage multiple priorities independently.
  • Comfortable working across scientific, clinical, commercial, and international teams.
  • Excellent written and spoken English.
  • Proactive, hands-on, and results-oriented mindset.
  • Comfortable working in a fast-paced start-up environment.
  • Willingness to travel in the US and internationally (approx. 30%)

Working Conditions

The environment is a typical start-up with an intrinsically motivated international team. Our company is an excellent place for rapid advancement and offers a promising opportunity to learn and share know-how in a very agile environment. The position requires the employee to go the extra mile when needed. We are looking for a team player who appreciates direct communication. The effort is rewarded with challenging tasks, the possibility to take responsibility, a highly driven team, and work serving a significant purpose. The job position comes with a competitive salary and a bonus for outstanding performance.

Employment Type: FULL_TIME