1

Assistant Biotech Paralegal Jobs (NOW HIRING)

Employment Counsel

Alameda, CA ยท On-site

$175K - $255K/yr

You will work closely with the General Counsel, other seasoned attorneys, paralegals, and support ... assist with the creation and regular review of policies, standards and business procedures ...

You will work closely with the General Counsel, other seasoned attorneys, paralegals, and support ... assist with the creation and regular review of policies, standards and business procedures ...

next page

Showing results 1-20

Assistant Biotech Paralegal information

See salary details

$12

$25

$37

How much do assistant biotech paralegal jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for assistant biotech paralegal in the United States is $25.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What are Assistant Biotech Paralegals?

Assistant Biotech Paralegals are legal professionals who support attorneys specializing in biotechnology law. They help with tasks such as preparing legal documents, conducting research on intellectual property and regulatory issues, and organizing case files related to patents, trademarks, and compliance in the biotech industry. Their work is crucial in ensuring that biotech companies adhere to applicable laws and regulations, especially regarding scientific innovations and product development. Assistant Biotech Paralegals typically work in law firms, corporate legal departments, or biotech companies, and may also assist with contract management and communications with government agencies.

What are the key skills and qualifications needed to thrive as an Assistant Biotech Paralegal, and why are they important?

To thrive as an Assistant Biotech Paralegal, you need a background in legal studies, familiarity with biotech terminology, and strong organizational skills, often supported by a paralegal certificate or relevant degree. Competence in legal research databases, document management systems, and intellectual property filing tools is typically required. Attention to detail, effective communication, and the ability to manage confidential information are standout soft skills in this role. These abilities are vital for supporting attorneys efficiently, maintaining compliance, and ensuring accuracy in complex biotech legal matters.

What are the typical responsibilities of an Assistant Biotech Paralegal in supporting patent filings and intellectual property matters?

As an Assistant Biotech Paralegal, you will play a key role in preparing and organizing documents required for patent filings, maintaining intellectual property databases, and assisting attorneys with patent prosecution and compliance matters. Daily tasks often include conducting prior art searches, coordinating with inventors and scientists to gather technical information, and managing deadlines for patent applications and responses. Collaboration with both legal and scientific teams is common, and attention to detail is crucial given the complexity of biotech patents. This role offers valuable exposure to both legal procedures and cutting-edge scientific innovations, providing a strong foundation for career growth within the legal or biotech industries.

What is the difference between Assistant Biotech Paralegal vs Patent Paralegal?

AspectAssistant Biotech ParalegalPatent Paralegal
Required CredentialsParalegal certification, life sciences knowledgeParalegal certification, IP law familiarity
Work EnvironmentBiotech firms, legal departments in science companiesIntellectual property law firms, corporate legal teams
Employer & Industry UsageBiotech and pharmaceutical industriesLegal firms specializing in patents and IP
Common Search & ComparisonYesYes

The Assistant Biotech Paralegal and Patent Paralegal roles share similarities in legal support and certification requirements. However, the Assistant Biotech Paralegal focuses on biotech-related legal tasks within scientific industries, while the Patent Paralegal specializes in intellectual property law, particularly patents. Both roles require paralegal certification, but their work environments and industry focus differ, making each role distinct in their respective legal and scientific contexts.

What cities are hiring for Assistant Biotech Paralegal jobs? Cities with the most Assistant Biotech Paralegal job openings:
What are the most commonly searched types of Biotech Paralegal jobs? The most popular types of Biotech Paralegal jobs are:
What states have the most Assistant Biotech Paralegal jobs? States with the most job openings for Assistant Biotech Paralegal jobs include:

Commercial Contracts Specialist

Kuros Biosciences, Inc.

Sandy Springs, GA โ€ข On-site

Full-time

Posted 11 days ago


Job description

Overview:
The Commercial Contracts Specialist supports the company's commercial, legal, and financial operations by managing the drafting, review, negotiation, and execution of commercial agreements. Reporting to the Corporate Attorney and working in close functional alignment with the VP of Finance and Sales leadership, this position serves as the primary contracting partner for the Sales organization.
This role ensures contracts are accurate, compliant, financially aligned, and processed efficiently through the company's Contract Lifecycle Management (CLM) system. The Specialist is essential to maintaining standardized contracting practices and supporting the company's growth in the medical device industry. This is a full-time,hybrid position.
Key Responsibilities:
Contract Drafting, Review, and Negotiation
  • Draft, review, and negotiate commercial agreements including sales agreements, distributor agreements, vendor contracts, NDAs, and pricing/rebate agreements.
  • Work within approved templates and playbooks; escalate non-standard or high-risk terms to the Corporate Attorney.
  • Provide timely support to Sales leadership with contract revisions and customer-facing documentation.

Contract Lifecycle Management
  • Administer the company's CLM platform, including template updates, workflow routing, reporting, and system maintenance.
  • Maintain accurate contract records, version control, audit trails, and document retention.

Finance & Pricing Coordination
  • Partner with Finance to validate pricing structures, rebate terms, discount programs, payment terms, and revenue-recognition considerations.
  • Ensure all financial terms are accurately incorporated into customer and vendor agreements.

Regulatory & Policy Compliance
  • Ensure contracts adhere to medical device and life sciences regulatory requirements, including:
    • Anti-Kickback Statute
    • Open Payments/Sunshine Act
    • Anti-corruption (FCPA and similar frameworks)
    • FDA-related quality, complaint, labeling, and distribution obligations
  • Support internal compliance reviews and audits related to contracting practices.

Cross-Functional Collaboration
  • Act as the primary contracting liaison for Sales, Legal, Finance, Operations, and other stakeholders.
  • Communicate contract requirements, timelines, risks, and necessary approvals across teams.

Process & Template Improvement
  • Assist with updating templates, clause libraries, and contract playbooks.
  • Identify opportunities to improve contracting workflows and reduce cycle times.
  • Promote consistency and efficiency across the contracting function.

Qualifications:
Required
  • Bachelor's degree in Business, Legal Studies, Finance, or a related field.
  • 3-5 years of commercial contracting experience in the medical device, life sciences, or pharmaceutical industry.
  • Experience drafting, reviewing, and negotiating commercial agreements.
  • Familiarity with healthcare compliance requirements and regulatory frameworks.
  • Experience with Contract Lifecycle Management (CLM) systems.
  • Strong attention to detail and ability to manage multiple priorities in a fast-paced environment.
  • Excellent written and verbal communication skills.

Preferred
  • Paralegal certification or equivalent legal training.
  • Experience supporting commercial or field sales teams.
  • Understanding of international medical device regulatory considerations.

Key Competencies
  • Contract negotiation and redlining
  • CLM system administration
  • Regulatory and compliance awareness
  • Cross-functional communication and collaboration
  • Process improvement and problem-solving
  • Ability to manage complexity and prioritize effectively

Travel Requirement:
  • Ability to travel domestic and international as needed

Physical Requirements and Work Conditions
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.
  • Mobility & Posture: May require occasional sitting, standing, walking, climbing, reaching, bending, or stooping.
  • Lifting/Carrying: May require lifting and carrying items 50 pounds or more, depending on the role.
  • Manual Dexterity: Frequent use of hands and fingers for typing, writing, grasping, and operating office or job-specific equipment.
  • Driving: Some roles may require the ability to operate a motor vehicle for extended periods and maintain a valid driver's license.

Specific requirements may vary by role. Contact an HR representative for details related to the position.
Our credentials
Kuros is a Swiss-headquartered biotech company, listed on the SIX Swiss Stock Exchange since 2016 (under symbol KURN). With additional operations in the Netherlands and the USA, we continue to grow our global team.
To deliver the ideal bone graft, you need the highest quality and quantity of scientific evidence behind it. We believe that this is a key differentiator for Kuros, given the urgent need to advance bone healing.
  • Listing on the SIX Swiss Exchange under the symbol KURN since 2016
  • A commercial & research footprint that spans >20 markets
  • Dozens of clinical and scientific expert Advisers
  • >25 orthobiologics-related patents
  • >400 patients evaluated in Level I, randomized controlled clinical trials
  • >20 well-controlled Level I-IV clinical trials initiated, including 6 that are complete1
  • Published Level I evidence published in Spine

Kuros Biosciences is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Kuros Biosciences complies with GDPR and the California Consumer Privacy Act (CCPA). View our CCPA Notice here.