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Entry Level Regulatory Affairs Biotech Jobs (NOW HIRING)

CorDx

Regulatory Affairs Specialist

Alpharetta, GA · On-site

About Us CorDx, a multi-national biotech organization, focused on pushing the limits of innovation ... Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required ...

CorDx

Regulatory Affairs Specialist

Alpharetta, GA · On-site

About Us CorDx, a multi-national biotech organization, focused on pushing the limits of innovation ... Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required ...

CorDx

Regulatory Affairs Specialist

Alpharetta, GA · On-site

About Us CorDx, a multi-national biotech organization, focused on pushing the limits of innovation ... Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required ...

CEDENT

Regulatory Associate

Boston, MA · On-site +1

... affairs, clinical research, or a related area within the pharmaceutical, biotech, or medical device industries. * Familiarity with regulatory submission processes and understanding of regulatory ...

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How much do entry level regulatory affairs biotech jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for entry level regulatory affairs biotech in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

What skills and qualifications are needed for an entry level regulatory affairs professional in biotech?

To thrive as an Entry Level Regulatory Affairs professional in biotech, you need a bachelor’s degree in life sciences or a related field, a solid understanding of regulatory guidelines, and strong analytical skills. Familiarity with regulatory submission systems (such as eCTD) and knowledge of FDA or EMA regulations are often required, and certifications like RAC can be advantageous. Attention to detail, effective communication, and organizational skills will help you manage documentation and collaborate with cross-functional teams. These skills are crucial for ensuring products comply with regulations, facilitating approvals, and supporting the company's success in a highly regulated industry.

What is an entry level regulatory affairs professional in biotech?

Entry level regulatory affairs roles in biotech involve supporting the processes required to ensure that products meet all regulatory standards and guidelines. These positions typically include tasks such as preparing and reviewing documentation, assisting with regulatory submissions, and staying updated on changing regulations. Entry level professionals often work under the guidance of senior staff and collaborate with other departments to help bring new products to market while maintaining compliance. These roles are ideal for recent graduates with degrees in life sciences or related fields who are interested in the intersection of science, business, and law.

What are common challenges faced by entry level regulatory affairs professionals in biotech?

Entry-level regulatory affairs professionals in biotech often encounter challenges such as navigating the complexity of regulatory guidelines and adapting to frequent changes in global compliance standards. They may also need to develop strong communication skills to coordinate effectively with cross-functional teams, including research, quality assurance, and manufacturing. Mastering the documentation process and learning how to interpret scientific data for regulatory submissions are key aspects that can initially be difficult but are essential for success in this role.
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Entry Level Regulatory Affairs Biotech jobs near you
Infographic showing various Entry Level Regulatory Affairs Biotech job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 9% Part Time, and 3% Contract. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Regulatory Affairs Associate

WHITE COLLAR TECHNOLOGIES INC

Boston, MA • On-site

$45K - $60K/yr

Full-time

Medical, Dental, Vision

Re-posted 5 days ago

Job description

    Job Description

    We have multiple openings for Life Science Quality Assurance Analysts, Regulatory Affairs Specialist, and Quality Control Analysts. All of these roles will interface with clients on different projects to provide consulting services.

    We are seeking entry-level experienced personnel or fresh graduate students willing to be trained as per our client's requirement and able to relocate. Most of our openings require 3-4 days' onsite presence at the client site.

    Minimum Qualification:

    0-3 years of experience in life science (pharmaceutical, biology, chemistry, bioinformatics) or engineering industry with a focus on information technology, clinical research, quality, regulatory affairs, manufacturing, or supply chain.

    Minimum bachelor’s degree in the above concentration.

    Valid US work authorization.

    Virtually able to participate in our training program.

    Able to relocate anywhere in the US.

    About

    White Collar Technologies Inc. is one of the fastest-growing pharmaceutical and life science consulting companies. We specialize in providing Information Technology, Engineering, Quality Assurance, and Project Management services. Our clients range from small Biotech and Gene Therapy companies to Large Biopharmaceutical companies.

    Our white-glove project placement includes the following benefits

    1. State-of-the-art client interview preparations with industry experts
    2. Relocation Package including airfare and hotel stay
    3. Competitive salary packages with full benefits package that includes PTO, Sick Time Off, Health Insurance (Medical, Dental, Vision)
    4. 1x1 supervision and support during client project delivery
    5. No-stress immigration visa processing with reputed attorney firms (CPT, OPT, H1B, H4 EAD, TN, L1, Green Card)

    Company Description

    White Collar Technologies is a boutique human capital consultancy firm specializing in information technology and engineering consulting for life science sector. Our consultants serve multitude of clients within Pharmaceutical, Biotech, Medical Device, Clinical Research and Healthcare verticals.
    We offer our workers Medical Dental and Vision healthcare benefits.