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Strategic Supply Chain Project Manager

Dallas, TX · On-site

$95K - $105K/yr

Partner with IT/ERP to refine planning parameters, master data quality, and visibility tools ... Experience in pharmaceutical, biotech, medical device, or other cGMP-regulated environments.

Jj

Director of PSC Operations

Dallas, TX · On-site

A minimum of 10 years of relevant industry experience in healthcare, biotech, pharmaceutical, or ... Master's degree, MBA, or other relevant graduate degree. * Experience with Commercial, Medicare ...

Pwc

Payer Healthcare Data Scientist, Manager

Dallas, TX

$99K - $232K/yr

... Master's Degree in Statistics, Computer Science, Applied Mathematics, Biotechnology preferred - Prior consulting or advisory firm experience preferred - Contributing to commercial analytics product ...

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Master In Biotechnology information

What is a master in biotechnology?

A Master in Biotechnology is a graduate-level degree program focused on the advanced study of biological processes and the use of technology to manipulate living organisms for applications in medicine, agriculture, and industry. Students learn about molecular biology, genetics, bioinformatics, and laboratory techniques, as well as how to apply these skills to develop new products and solutions. This degree prepares graduates for careers in research, pharmaceuticals, healthcare, environmental management, and biotechnology companies, or for further study at the doctoral level.

What are typical career paths for a master in biotechnology, and how can they progress within the industry?

Graduates with a Master in Biotechnology can pursue diverse career paths, such as research scientist, quality control analyst, regulatory affairs specialist, or roles in product development and project management. Advancement often involves taking on leadership responsibilities, such as managing teams or projects, or specializing further in areas like bioinformatics or clinical research. Many professionals also transition into roles in biotech startups, pharmaceuticals, or government agencies, and may further their expertise through certifications or a doctoral degree. Networking, continuous skill development, and staying updated with industry trends are key to progressing within the biotechnology sector.

What are the key skills and qualifications needed to thrive as a master in biotechnology, and why are they important?

To thrive as a Master in Biotechnology, you need advanced knowledge in molecular biology, genetics, and laboratory techniques, typically supported by a master's degree in biotechnology or a related field. Familiarity with bioinformatics tools, PCR, and laboratory information management systems (LIMS) is essential, and certifications in laboratory safety can be advantageous. Strong problem-solving, critical thinking, and teamwork skills distinguish top professionals in this field. These competencies enable effective research, innovation, and collaboration in the rapidly evolving biotech industry.

What is the difference between Master In Biotechnology vs Biotechnology Research Associate?

CriteriaMaster In BiotechnologyBiotechnology Research Associate
Required CredentialsMaster's degree in Biotechnology or related fieldBachelor's or Master's degree in Biotechnology or related field
Work EnvironmentLaboratories, research facilities, academic institutionsLaboratories, biotech companies, research organizations
Employer & Industry UsageAcademic, research, biotech industryBiotech companies, research labs, pharmaceutical firms
Common Search & ComparisonYesYes

The Master In Biotechnology typically prepares individuals for advanced roles in research, development, and academia, requiring a master's degree. A Biotechnology Research Associate usually holds a bachelor's or master's degree and works directly in research projects within biotech companies or labs. While both roles involve laboratory work and research, the Master's degree often leads to more senior or specialized positions.

Is a Master in Biotechnology a good career?

A Master in Biotechnology prepares individuals for careers in research, development, and quality control within biotech, pharmaceutical, and healthcare industries. It offers opportunities in laboratory work, product development, and regulatory roles, often requiring skills in molecular biology, data analysis, and laboratory techniques. The field is growing due to advances in medical research and biomanufacturing, making it a viable career path for those interested in science and innovation.

What can I do with a master in biotechnology?

A master in biotechnology prepares individuals for roles such as research scientist, bioprocess engineer, quality control analyst, or laboratory manager in industries like pharmaceuticals, healthcare, agriculture, and environmental science. Graduates often work with laboratory techniques, data analysis, and regulatory compliance, and may pursue certifications or further specialization to advance their careers.

What are popular job titles related to Master In Biotechnology jobs in Dallas, TX?

For Master In Biotechnology jobs in Dallas, TX, the most frequently searched job titles are:

What job categories do people searching Master In Biotechnology jobs in Dallas, TX look for?

The top searched job categories for Master In Biotechnology jobs in Dallas, TX are:

What cities near Dallas, TX are hiring for Master In Biotechnology jobs?

Cities near Dallas, TX with the most Master In Biotechnology job openings:

Master In Biotechnology jobs near you
Infographic showing various Master In Biotechnology job openings in Dallas, TX as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 85% In-person, and 15% Remote job distribution.

REGULATORY SPECIALIST - CRI

Methodist Health System

Dallas, TX • On-site

Full-time

Re-posted 8 days ago

Job description

Hours of Work :
8am-5pm
Days Of Week :
M-F
Work Shift :
Job Description :
Your Job:
The Regulatory Specialist will perform expertise in the regulatory component of all clinical research trials to include, but not limited to; Phase II and IV clinical, investigator initiated trials (IITs), and retrospective analysis of clinical data. The Regulatory Specialist will support the mission, vision, values, and strategies of the Methodist Health System.
Your Job Requirements:
• Bachelor's degree required; Master's degree preferred
• CCRC or CCRP (preferred)
• GCP certification (preferred)
• 1 year of experience in a medical or clinical setting (required)
• 1 year of experience in clinical research (required)
• 1 year of experience in research regulatory affairs (required)
• Strong proficiency using Microsoft Office products
• Superior oral and written communication skills
• Strong process orientation
• Detail oriented, logical, and methodological approach to problem solving
• Ability to provide vision and leadership.
Your Job Responsibilities:
• Communicate clearly and openly
• Build relationships to promote a collaborative environment
• Be accountable for your performance
• Always look for ways to improve the patient experience
• Take initiative for your professional growth
• Be engaged and eager to build a winning team
• Review clinical research protocols to determine logistical components of regulatory requirements
• Obtain and facilitate tracking of relevant regulatory documents for clinical trials submission and management.
• Maintain appropriate communications between sponsors, investigators, other research team members for clinical trials assigned.
• Assist in the development of clinical trial documents for signature of principal investigator and approval by the IRB.
• Create and/or adapt clinical trial informed consent documents for Institutional Review Board (IRB) submission.
• Maintain regulatory documents in accordance with International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) guidelines.
• Attend study specific training, investigator meetings as assigned, and MHS required training.
• Facilitate informed consent process for principal and sub-investigators.
• Assist clinical research coordinators in the identification and reporting of appropriate adverse events in accordance with Food and Drug Administration, sponsor protocol, and IRB regulations and guidelines.
• Prepare and submit amendments to protocols and informed consent documents as required.
Methodist Health System is a faith-based organization with a mission to improve and save lives through compassionate, quality healthcare. For nearly a century, Dallas-based Methodist Health System has been a trusted choice for health and wellness. Named one of the fastest-growing health systems in America by Modern Healthcare, Methodist has a network of 12 hospitals (through ownership and affiliation) with nationally recognized medical services, such as a Level I Trauma Center, multi-organ transplantation, Level III Neonatal Intensive Care, neurosurgery, robotic surgical programs, oncology, gastroenterology, and orthopedics, among others. Methodist has more than two dozen clinics located throughout the region, renowned teaching programs, innovative research, and a strong commitment to the community. Our reputation as an award-winning employer shows in the distinctions we've earned:
  • Great Place to Work Certified 2026-2027
  • Glassdoor's Best Places to Work 2025 & 2026
  • Glassdoor's Best Places to Work in Healthcare, Biotech & Pharma 2026
  • TIME's Best Companies for Future Leaders 2025 & 2026
  • Newsweek's America's Most Admired Workplaces 2026
  • Glassdoor's Best-Led Companies 2025
  • Fortune Best Workplaces in Health Care 2025
  • Military Friendly Gold Employer 2025
  • Becker's Hospital Review 150 Top Places to Work in Healthcare 2025
  • Newsweek's Americas Greatest Workplaces 2025

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