ZipRecruiter

Log In

2

Fda Entry Level Jobs in Dallas, TX (NOW HIRING)

Neurology Rare Disease Center

Be Seen First

Clinical Research Coordinator (CRC)

Flower Mound, TX · On-site

$50K - $70K/yr

This is not an entry-level role and requires a high level of accountability, ownership, and the ... Ensure strict adherence to GCP, FDA regulations, and protocol requirements * Maintain high-quality ...

BE&K Building Group

Project Manager

Dallas, TX · On-site

... the entry level to around $20M at the upper range of the position. PRINCIPLE AREAS OF ... Ensure all construction activities comply with industry standards, GMP regulations, and FDA ...

BE&K Building Group

Project Manager

Dallas, TX · On-site

... the entry level to around $20M at the upper range of the position. PRINCIPLE AREAS OF ... Ensure all construction activities comply with industry standards, GMP regulations, and FDA ...

BE&K Building Group

Project Manager

Dallas, TX · On-site

... the entry level to around $20M at the upper range of the position.PRINCIPLE AREAS OF ... Ensure all construction activities comply with industry standards, GMP regulations, and FDA ...

next page

Showing results 1-20

All JobsFda JobsFda Entry Level JobsFda Entry Level Jobs in Dallas, TX

Fda Entry Level information

See Dallas, TX salary details

$20.2K

$47.2K

$96.2K

How much do fda entry level jobs pay per year?

As of Aug 9, 2026, the average yearly pay for fda entry level in Dallas, TX is $47,224.00, according to ZipRecruiter salary data. Most workers in this role earn between $34,537.00 and $50,819.00 per year, depending on experience, location, and employer.

What are the typical responsibilities of an FDA entry level?

In an FDA Entry Level role, you may be tasked with supporting regulatory submissions, compiling and reviewing documentation, and ensuring compliance with FDA guidelines. Your responsibilities might also include data entry, assisting with laboratory tests or inspections, and helping prepare reports for internal and external stakeholders. You could work closely with scientists, regulatory affairs specialists, and quality assurance teams, which provides valuable exposure to the regulatory process and industry best practices. This hands-on experience helps you build foundational knowledge and opens the door to advancement to more specialized or senior roles over time.

What are the key skills and qualifications needed for an FDA entry level?

To thrive in an FDA Entry Level position, candidates typically need a bachelor’s degree in life sciences, pharmacy, or a related field, along with basic knowledge of regulatory processes. Familiarity with regulatory documentation, data entry systems, and software like Microsoft Office is important and some roles may require training in Good Laboratory Practice (GLP) or similar certifications. Detail orientation, analytical thinking, and strong written and verbal communication skills help candidates excel and collaborate effectively. These competencies ensure accuracy, compliance, and smooth communication in highly regulated environments.

What qualifications do I need for FDA entry level jobs?

FDA entry-level jobs typically require a bachelor's degree in a relevant field such as biology, chemistry, or health sciences. Strong attention to detail, good communication skills, and familiarity with regulatory guidelines and documentation are also important qualifications.

What is an FDA entry level?

An FDA entry-level job is a starting position within the U.S. Food and Drug Administration, typically suited for recent graduates or individuals with minimal experience in regulatory affairs, public health, or scientific research. These roles can include positions in drug evaluation, food safety, compliance, and laboratory research. Responsibilities often involve data analysis, regulatory review, inspections, and assisting senior staff with policy implementation. Entry-level professionals gain valuable experience in federal regulations, public health policies, and scientific evaluations, which can lead to career advancement within the agency.

What are the most commonly searched types of Fda jobs in Dallas, TX? The most popular types of Fda jobs in Dallas, TX are:
What are popular job titles related to Fda Entry Level jobs in Dallas, TX? For Fda Entry Level jobs in Dallas, TX, the most frequently searched job titles are:
What job categories do people searching Fda Entry Level jobs in Dallas, TX look for? The top searched job categories for Fda Entry Level jobs in Dallas, TX are:
What cities near Dallas, TX are hiring for Fda Entry Level jobs? Cities near Dallas, TX with the most Fda Entry Level job openings:
Fda Entry Level jobs near you
Infographic showing various Fda Entry Level job openings in Dallas, TX as of August 2026, with employment types broken down into 33% Full Time, 33% Part Time, and 34% Contract. Highlights an 100% In-person job distribution, with an average salary of $47,224 per year, or $22.7 per hour.

Clinical Research Coordinator (CRC)

Neurology Rare Disease Center

Flower Mound, TX • On-site

$50K - $70K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Be Seen First

After you apply to this job, you can share why you’re interested to jump to the top of the candidate list.

Job description

Position Summary

We are seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical trials from start-up through close-out. This role requires strong organizational skills, regulatory knowledge, and the ability to work closely with patients, investigators, sponsors, and coordinate activities across both on-site and remote PRN staff. Candidates must be willing to travel, including attendance at Investigator Meetings (IMs), as required. This is not an entry-level role and requires a high level of accountability, ownership, and the ability to operate independently with minimal oversight.

Key Responsibilities

  • Independently coordinate multiple clinical trials from startup to close-out
  • Lead patient recruitment, screening, consenting, and retention strategies
  • Conduct study visits, assessments, and protocol-specific procedures
  • Ensure strict adherence to GCP, FDA regulations, and protocol requirements
  • Maintain high-quality source documentation and EDC data entry (real-time, audit-ready)
  • Manage investigational product accountability and study logistics
  • Serve as the primary point of contact for sponsors, CROs, and monitors
  • Prepare for and confidently support monitoring visits, audits, and FDA inspections
  • Identify inefficiencies and proactively improve workflows

Performance Expectations

  • Maintain audit-ready documentation at all times (ALCOA+ compliant)
  • Ensure timely and accurate EDC data entry (real-time or within defined timelines)
  • Demonstrate ownership of assigned studies with minimal oversight
  • Maintain readiness for monitoring visits, audits, and FDA inspections at all times
  • Proactively identify, document, and escalate issues, risks, and protocol deviations

Work Environment

  • Fast-paced, high-accountability clinical research setting
  • Requires ability to manage competing priorities and adapt to changing study demands
  • High level of autonomy with expectation of independent problem-solving

Qualifications

  • Bachelor’s degree in life sciences, healthcare, or related field (preferred)
  • 2+ years of clinical research experience (CRC experience preferred)
  • Strong knowledge of GCP, FDA, and IRB processes
  • Experience with EDC systems and clinical trial documentation
  • Excellent organizational, communication, and multitasking skills
  • Ability to manage multiple studies in a fast-paced environment

Highly Preferred (but not required)

  • Experience in neurology, neuromuscular, or rare disease trials
  • Experience in industry-sponsored trials
  • Phlebotomy and/or clinical skills
  • Certification (CCRC, CCRP, or equivalent)
  • Experience in reviewing patient medical records for pre-screening
  • Experience with CRIO preferred but not required

Compensation & Benefits

  • Competitive salary (based on experience; typical CRC range (~$50K–$70K/year) 
  • Health, dental, and vision insurance
  • Paid time off
  • Opportunities for growth and leadership within a rapidly expanding research center

Company Description

Neurology Rare Disease Center is a growing neurology and clinical research center dedicated to advancing care for patients with rare neuromuscular diseases. We are committed to high-quality, patient-centered research and innovation. We are building a team of people who care deeply about patients and take pride in doing things the right way.