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Biotech Operations Jobs in Dallas, TX (NOW HIRING)

Jj

Associate Director, PSC Operations

Dallas, TX · On-site

Customer Service Operations Job Category: People Leader All Job Posting Locations: Charlotte, North ... biotech or other healthcare industry roles * Proven leadership skills with the ability to inspire ...

Astrix Inc

Senior Logistics Specialist

Plano, TX · On-site

$80K - $90K/yr

... biotechnology client. Title: Senior Logistics Specialist Location: Plano, TX (Onsite) Schedule ... Collaborate with Warehouse, Shipping, Operations, and other internal teams to ensure successful and ...

Astrix Inc

Senior Logistics Specialist

Plano, TX · On-site

$80K - $90K/yr

... biotechnology client. Title: Senior Logistics Specialist Location: Plano, TX Schedule: Monday ... Collaborate with Warehouse, Shipping, Operations, and other internal teams to ensure successful and ...

Iterative Health

Director, Life Sciences

Dallas, TX · Hybrid

... biotechnology and pharmaceutical organizations. * Strong understanding of the clinical trial ecosystem, including sponsors, CROs, site networks, and research operations. * Established network of ...

Novartis

Ops Manager - Project Delivery & Mfg.

Denton, TX · On-site

$98K - $183K/yr

Experience supporting startup, operational readiness, manufacturing operations, or organizational buildout activities. * Experience in pharmaceutical, biotechnology, Good Manufacturing Practice, or ...

Immunedge Inc

Staff Accountant

Plano, TX · On-site

$70K - $90K/yr

... operations in a fast-moving, early-stage biotech. This is a great opportunity for someone early in their career who wants broad exposure and room to grow. Strong candidates will be detail-oriented ...

ImmunEdge, Inc

Staff Accountant

Plano, TX · On-site

$70K - $90K/yr

... operations in a fast-moving, early-stage biotech. This is a great opportunity for someone early in their career who wants broad exposure and room to grow. Strong candidates will be detail-oriented ...

ImmunEdge Inc.

Accounting Specialist

Plano, TX · On-site

$70 - $90/hr

... operations in a fast-moving, early-stage biotech. This is a great opportunity for someone early in their career who wants broad exposure and room to grow. Strong candidates will be detail-oriented ...

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Showing results 21-40

All JobsBiotech Operations JobsBiotech Operations Jobs in Dallas, TX

Biotech Operations information

See Dallas, TX salary details

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$52

How much do biotech operations jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for biotech operations in Dallas, TX is $25.96, according to ZipRecruiter salary data. Most workers in this role earn between $17.60 and $29.95 per hour, depending on experience, location, and employer.

What is biotech operations?

Biotech operations refer to the management and coordination of processes involved in developing, manufacturing, and distributing biotechnology products. This includes overseeing laboratory research, quality control, regulatory compliance, production scaling, and supply chain logistics. Professionals in biotech operations ensure that products such as pharmaceuticals, vaccines, or genetically engineered organisms are produced safely, efficiently, and in compliance with industry standards. Their work is critical in bringing scientific discoveries from the lab to market and ultimately to patients or consumers.

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

Thriving in Biotech Operations requires a solid background in life sciences or engineering, experience with regulatory compliance, and a relevant degree such as a B.S. or M.S. in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), quality management systems (QMS), and certifications like Six Sigma or GMP training are highly valuable. Excellent problem-solving abilities, attention to detail, and strong collaboration skills help individuals excel and adapt in dynamic environments. These competencies are essential for ensuring operational efficiency, regulatory adherence, and successful product development in the biotech industry.

What are some common challenges faced in biotech operations, and how can new team members effectively navigate them?

Biotech Operations professionals often encounter challenges such as stringent regulatory compliance, maintaining production timelines, and managing cross-functional communication between research, quality, and manufacturing teams. New team members can navigate these challenges by proactively seeking mentorship, staying organized with project management tools, and maintaining open communication channels with colleagues in related departments. Embracing a mindset of continuous learning and adaptability is also crucial, as processes and technologies in biotech are constantly evolving.

What is the difference between Biotech Operations vs Laboratory Technician?

AspectBiotech OperationsLaboratory Technician
Required CredentialsBachelor's degree in biotech, biology, or related field; sometimes certifications in GMP or quality assuranceAssociate's or bachelor's degree in biology, chemistry, or related field; lab safety certifications often preferred
Work EnvironmentManufacturing facilities, quality control labs, production linesResearch labs, clinical labs, testing facilities
Employer & Industry UsageBiotech companies, pharmaceutical manufacturers, biotech startupsResearch institutions, hospitals, biotech and pharma labs

Biotech Operations roles focus on managing production processes, quality assurance, and ensuring compliance in manufacturing settings. Laboratory Technicians primarily perform experiments, testing, and data collection in research or clinical labs. While both roles require scientific knowledge, Biotech Operations emphasizes process management and compliance, whereas Laboratory Technicians focus on hands-on lab work and data analysis.

What are popular job titles related to Biotech Operations jobs in Dallas, TX?

For Biotech Operations jobs in Dallas, TX, the most frequently searched job titles are:

What job categories do people searching Biotech Operations jobs in Dallas, TX look for?

The top searched job categories for Biotech Operations jobs in Dallas, TX are:

Biotech Operations jobs near you
Infographic showing various Biotech Operations job openings in Dallas, TX as of August 2026, with employment types broken down into 83% Full Time, 13% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $54,001 per year, or $26 per hour.

Clinical Operations Manager

Verily Life Sciences

Dallas, TX • On-site

Full-time

Re-posted 5 days ago

Key responsibilities

  • Author and establish critical study documentation, including Clinical Protocols, Informed Consent Forms (ICFs), and participant-facing materials.

  • Implement study operational plans, including the Integrated Quality Risk Management Plan (IQRMP) and Study Monitoring Plan, alongside clinical SOPs.

  • Serve as the primary contact for clinical sites, managing site operations, protocol deviations, adverse event evaluations, and IRB reporting; and oversee electronic Trial Master Files (eTMFs) to ensure full GCP compliance, regulatory adherence, and continuous audit readiness.

Job description

Who We Are
Verily Health is a data platform and technology company purpose-built to power AI-enabled precision health solutions that accelerate research and improve care for individuals and communities. Uniquely positioned at the intersection of technology, data science, and healthcare, Verily transforms multimodal health data into insights, models, and actions that make healthcare more personalized, predictive, and precise.
Description
The Clinical Operations Manager serves as a dedicated functional expert within a cross-functional (XFN) team, contributing specific subject matter expertise (SME) to ensure operational execution of clinical studies. This role focuses directly on driving core operational milestones, clinical study documentation, and compliance frameworks from study design through study closeout. The Clinical Operations Manager owns critical study documentation, risk management strategy, site selection and qualification, monitoring oversight, and safety/deviation workflows from study start-up through to study close-out, collaborating within cross-functional teams to drive successful end-to-end study execution.
Responsibilities
  • Author and establish critical study documentation, including Clinical Protocols, Informed Consent Forms (ICFs), and participant-facing materials.
  • Implement study operational plans, including the Integrated Quality Risk Management Plan (IQRMP) and Study Monitoring Plan, alongside clinical SOPs.
  • Serve as the primary contact for clinical sites, managing site operations, protocol deviations, adverse event evaluations, and IRB reporting; and, oversees electronic Trial Master Files (eTMFs) to ensure full GCP compliance, regulatory adherence, and continuous audit readiness.
  • Support the research agenda across teams, including managing research timelines across the business from inception to publication.
  • Work across the Research/EvGen/Clinical Quality Teams to provide project management support for projects that further business strategy for evidentiary claim development.

Qualifications
Minimum Qualifications
  • Bachelor's degree in a life sciences, healthcare, or technical field, or equivalent practical experience.
  • 4+ years of direct experience in clinical operations, clinical trial management, or a related operational role within healthcare or biotechnology.
  • Direct experience drafting clinical study documentation (protocols, ICFs) and managing eTMF systems.
  • Strong subject matter expertise (SME) working inside cross-functional (XFN) project or product teams.

Preferred Qualifications
  • Deep familiarity with GCP compliance, regulatory submission considerations, and clinical SOP development.
  • Excellent communication skills with the ability to provide clear clinical operational guidance to cross-functional stakeholders.
  • Strong organizational skills that ensure development of evidentiary claims across the organization consistent with the commercial needs.
  • Project management certification; experience with JIRA.

Qualified applicants must not require employer sponsored work authorization now or in the future for employment in the United States.
The US base salary range for this full-time position is $119,000 - $179,000 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.
Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits.
Verily Health Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click here. If you'd like more information on your EEO rights under the law, please click here.
If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form.

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