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Scientific Affairs Associate Jobs (NOW HIRING)

Lancesoft

Regulatory Affairs Associate II

Princeton, NJ · On-site

$50 - $55/hr

Regulatory Affairs Associate II Hybrid working once fully trained. More on site presence whilst ... Education & Qualifications: BS in science or relevant field. Pharmaceutical and Regulatory ...

Berlin Heart Inc

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Jr RA/QA Associate

The Woodlands, TX · On-site

The Junior Quality/Regulatory Affairs Associate under the direction of the VP of Quality and ... Bachelor/Master of Science in related field of study with exposure to medical devices. REQUIRED ...

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How much do scientific affairs associate jobs pay per hour?

As of May 31, 2026, the average hourly pay for scientific affairs associate in the United States is $31.48, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $40.14 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Scientific Affairs Associate, and why are they important?

To thrive as a Scientific Affairs Associate, a strong background in life sciences, analytical thinking, and often an advanced degree (such as MS or PhD) are essential. Familiarity with regulatory databases, scientific literature search tools, and document management systems is typically required, along with experience in preparing scientific and regulatory documents. Excellent communication, attention to detail, and the ability to collaborate with cross-functional teams are standout soft skills for this role. These competencies are crucial for ensuring accurate scientific communication, regulatory compliance, and effective support of product development and approval processes.

How does a Scientific Affairs Associate typically collaborate with cross-functional teams in a healthcare or pharmaceutical company?

As a Scientific Affairs Associate, you will frequently work alongside clinical, regulatory, and marketing teams to ensure scientific accuracy and compliance in all communications and materials. Collaboration often involves reviewing clinical data, preparing scientific content for internal and external stakeholders, and supporting product launches or educational initiatives. This role requires clear communication and the ability to translate complex scientific information for diverse audiences, making teamwork and adaptability essential for success.

What does a Scientific Affairs Associate do?

A Scientific Affairs Associate supports the development and communication of scientific information within organizations such as pharmaceutical, biotechnology, or medical device companies. Their responsibilities often include reviewing and summarizing scientific literature, preparing technical documentation, assisting with regulatory submissions, and serving as a liaison between research, regulatory, and commercial teams. They play a crucial role in ensuring scientific accuracy in company materials and helping translate complex data into understandable information for both internal and external stakeholders. This position typically requires a strong background in science, excellent communication skills, and attention to detail.
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Scientific Affairs Associate jobs near you
Infographic showing various Scientific Affairs Associate job openings in the United States as of May 2026, with employment types broken down into 10% As Needed, 55% Full Time, 16% Part Time, 12% Temporary, 1% Contract, and 6% Nights. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $65,473 per year, or $31.5 per hour.
Regulatory Affairs Associate

Regulatory Affairs Associate

WHITE COLLAR TECHNOLOGIES INC

Boston, MA • On-site

$45K - $60K/yr

Full-time

Medical, Dental, Vision

Posted 21 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.