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Drug Development Jobs in Austin, TX (NOW HIRING)

VP, Research and Development

Round Rock, TX ยท On-site

$240 - $360/hr

VP, Research and Development at Attaineo The VP of Research & Development will define and execute the company's R&D strategy, ensuring the timely delivery drug development, optimization and ...

Ability to apply drug development knowledge during production of high quality statistical analyses. * Perform sample size calculations for a variety of scenarios and study designs. * Leads projects ...

Significant experience in oncology drug development. * Experience serving as Medical Monitor for interventional oncology clinical trials. * Demonstrated experience leading cross-functional clinical ...

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve ...

Bilingual Phlebotomist

Pflugerville, TX ยท On-site

$16 - $20/hr

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve ...

Bilingual Phlebotomist

Pflugerville, TX ยท On-site

$16 - $20/hr

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve ...

The Development Associate works with the Development and Communications Manager in supporting the ... Must be able to pass a criminal background check, drug screening, and moving violation report

Senior Clinical Scientist

Austin, TX ยท Remote

$150K - $200K/yr

Deep understanding of oncology drug development; experience in metabolism, nutrition, or biomarker-driven approaches is a plus * Working knowledge of GCP, ICH guidelines, and global regulatory ...

Senior Clinical Scientist

Austin, TX ยท On-site

$150K - $200K/yr

Deep understanding of oncology drug development; experience in metabolism, nutrition, or biomarker-driven approaches is a plus * Working knowledge of GCP, ICH guidelines, and global regulatory ...

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Drug Development information

See Austin, TX salary details

$32.7K

$76.8K

$131.8K

How much do drug development jobs pay per year?

As of Aug 14, 2026, the average yearly pay for drug development in Austin, TX is $76,758.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,000.00 and $89,700.00 per year, depending on experience, location, and employer.

What career develops drugs?

A career in drug development typically involves roles such as pharmacologist, medicinal chemist, clinical researcher, or regulatory affairs specialist. These professionals work in laboratories, research institutions, or pharmaceutical companies to discover, test, and bring new drugs to market, often requiring knowledge of biology, chemistry, and regulatory processes.

What is the difference between Drug Development vs Pharmacologist?

AspectDrug DevelopmentPharmacologist
Required CredentialsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields; often requires experience in clinical trialsDegree in Pharmacology, Pharmacy, or related fields; may require licensing or certification for clinical practice
Work EnvironmentResearch labs, pharmaceutical companies, clinical trial sitesResearch labs, hospitals, academic institutions, regulatory agencies
Industry UsageDeveloping new drugs, overseeing clinical trials, regulatory submissionsStudying drug effects, mechanisms, safety, and efficacy; advising on drug use

While both roles are integral to the pharmaceutical industry, Drug Development focuses on creating and bringing new drugs to market through research, testing, and regulatory processes. Pharmacologists primarily study how drugs interact with biological systems, often working in research or clinical settings to understand drug effects and safety. The two roles often collaborate but differ in their core responsibilities and career focus.

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

To thrive in Drug Development, you need a strong background in pharmaceutical sciences, biology, or chemistry, often supported by an advanced degree (e.g., PhD, PharmD, or MSc). Familiarity with regulatory compliance, clinical trial management systems, and data analysis software such as SAS or R is typically required. Excellent problem-solving, project management, and cross-functional communication skills help professionals excel in this multidisciplinary field. These competencies ensure that new drugs are developed safely, efficiently, and in accordance with regulatory standards.

What is drug development?

Drug development is the process of bringing a new pharmaceutical drug to market. It involves several stages, including drug discovery, preclinical research, clinical trials, and regulatory approval. Each stage is designed to ensure the safety, efficacy, and quality of the drug before it can be made available to patients. The entire process can take several years and requires collaboration between scientists, clinicians, regulatory agencies, and pharmaceutical companies.

How much do drug development professionals make?

Drug development professionals, including roles such as research scientists and clinical trial managers, typically earn between $70,000 and $130,000 annually, depending on experience, education, and location. Entry-level positions may start lower, while senior roles with advanced skills and certifications can exceed this range.

How do you get into drug development?

To enter drug development, individuals typically need a background in life sciences such as biology, chemistry, or pharmacology, often supported by a relevant bachelor's or advanced degree. Gaining experience through internships, research projects, or entry-level roles in pharmaceutical or biotech companies can be valuable, along with developing skills in laboratory techniques, data analysis, and regulatory compliance.

What are the typical stages of collaboration between different teams in a drug development role?

In drug development, professionals regularly collaborate across multidisciplinary teams, including research scientists, clinical trial coordinators, regulatory affairs specialists, and manufacturing experts. Early stages involve close work with research and discovery teams to identify promising compounds, followed by coordination with clinical teams during trial phases, and finally with regulatory and production teams as the drug moves toward approval and commercialization. Effective communication and cross-functional teamwork are essential, as each stage relies on timely data sharing and joint problem-solving to navigate complex challenges.

What cities near Austin, TX are hiring for Drug Development jobs?

Cities near Austin, TX with the most Drug Development job openings:

Infographic showing various Drug Development job openings in Austin, TX as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $76,758 per year, or $36.9 per hour.

VP, Research and Development

Attaineo

Round Rock, TX โ€ข On-site

$240 - $360/hr

Other

Posted 9 days ago


Job description

VP, Research and Development at Attaineo

The VP of Research & Development will define and execute the company's R&D strategy, ensuring the timely delivery drug development, optimization and enterprise deliverables that are innovative, creative, cost effective and cutting-edge scientific solutions. This role will create and execute the company's overall technology vision, manage the appropriate development methodologies, and create a high performing development team to deliver high-quality solutions to the market.

RELATIONSHIPS

Reports to the CEO. The position works closely with the Quality, Manufacturing, Regulatory and Clinical teams. Will establish internal and external relationships, which may include interactions with various stakeholders, clients, internal/external consultants and organizations, as needed.

DUTIES AND RESPONSIBILITIES
  • Responsible for the development of innovative scientific and production strategies to support business expansion and new areas of opportunity.
  • Oversees the development of chemical synthetic or other pathways for compounds of interest in line with our business strategy.
  • Provide strategic leadership to develop and implement a comprehensive development strategy for the cannabis/psychedelic portfolio, focusing on achieving milestones.
  • Collaborates with related functions including Management, Quality Assurance, Manufacturing and others on the development and future deployment of new molecules and formulations.
  • Collaborates closely with customers and other partners to align goals and achieve mutual satisfaction and benefit.
  • Provide technical leadership for the design and execution of Quality-by-Design (QbD) product development studies and development of scalable manufacturing process for parenteral drugs.
  • Manage Formulation Development for new products. Provide optimized formulations for performance and stability, study material compatibility and evaluate sterilization options.
  • Create or enhance market acceptance of the companyโ€™s products.
  • Maintain effective communication with internal and external stakeholders, clients, including investors, partners, and regulatory bodies.
  • Present development updates, strategic insights, and risk assessments to the executive team and board of directors.
  • Develop and manage the development budget, ensuring optimal allocation of resources to achieve project milestones and strategic objectives.
  • Demonstrate strong leadership skills through the supervision, coaching and mentoring of others.
  • Responsible for development of scalable manufacturing processes that can be executed in line and related regulatory agencies.
  • Support troubleshooting of existing commercial processes as requested.
  • Provide data and support for the creation, submission and approval or regulatory documents including, for example, Drug Master Files, INDโ€™s, (A)NDAโ€™s and the like.
QUALIFICATIONS (Education, Experience, Knowledge, and Skills)
  • She/he should have at least 15 years of experience and/or knowledge in organic synthesis, process development and enabling technologies.
  • Must have relevant industry experience in pharmaceutical/biotechnology small molecule development and/or business development.
  • Contract Manufacturing experience (API and Drug Product), drug delivery, and contract research desired.
  • Advanced degree (MD, PhD, or equivalent) in a life sciences or medical discipline.
  • Proven track record of successful leadership in API, formulation, and product development, preferably within the cannabis/psychedelic area.
  • Understand overall drug development process, regulatory guidelines, and CMC strategy in US, with global experience a plus.
  • Ability to effectively interact with and influence suppliers/vendors, regulators, global partners or affiliates, industry executives, and trade organizations.
  • Must have demonstrated managerial experience in leading a team of scientists, in the areas of R&D, Formulation and Quality preferred.
  • Strong analytical problem-solving experience: demonstrated prior experience in leading and motivating teams to conceptualize and develop innovative and creative solutions that are robust and sustainable.
  • Preferred: - Experience with Tradeshows/Conferences - Established Industry Connections - Technical Writing Experience
  • Ability to prioritize and manage multiple complex situations, where precedent may not have been established; strong decision making and the ability to work through ambiguity and uncertainty.
  • Strong communication and interpersonal skills
WORKING CONDITIONS / PHYSICAL REQUIREMENTS
  • Standard office environment.
  • Flexibility and ability to multitask and adjust job responsibilities as needed.
  • Excellent command of the English language (spoken and written), strong interpersonal skills, and exceptionally strong communication skills.
  • Highly effective presentation skills and ability to explain to both a scientific and non-scientific audience.
  • Ability to effectively work with other departments and assist as needed as a scientific reference point.
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