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Biotech Contract Manager Jobs in Texas (NOW HIRING)

Experienced Contract Manager

Irving, TX · On-site +1

$82K - $110K/yr

Provide mentorship and guidance to contract specialists and junior managers Qualifications ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

Experienced Contract Manager

Irving, TX · On-site

$82K - $110K/yr

Contract and budget negotiation experience; * 3+ years of management or oversight experience ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

Be Seen First

Manage routine contract negotiations with limited supervision. * Partner with internal and external ... Sponsor-side pharma or biotech contracting experience preferred. * Clinical site budgeting and ...

Be Seen First

Manage routine contract negotiations with limited supervision. * Partner with internal and external ... Sponsor-side pharma or biotech contracting experience preferred. * Clinical site budgeting and ...

Senior Contract Specialist

Irving, TX · On-site

$91K/yr

Manages all required contractual agreements with investigator sites. This includes distribution ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

Senior Contract Specialist

Irving, TX · On-site +1

$91K/yr

Manages all required contractual agreements with investigator sites. This includes distribution ... biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the ...

Clinical Contract Associatepositionwith Sylmar, CA, Santa Clara, CA, Plano, TXor Maple Grove, MN as ... This is an in-office position Position Summary Working under the direction of manager, provides ...

Clinical Contract Associatepositionwith Sylmar, CA, Santa Clara, CA, Plano, TXor Maple Grove, MN as ... This is an in-office position Position Summary Working under the direction of manager, provides ...

... Contract Research, Development, Testing, and Consulting Organization (CRO) supporting ... This individual will drive new business opportunities for CRO services with biotech, pharmaceutical ...

Staff Accountant

Plano, TX · On-site

$70K - $90K/yr

Join us in shaping the future of biotechnology. Together, we can changelives. Position: ImmunEdge ... Exposure to AP automation, T&E platforms, forecasting platforms, or contract management systems ...

Staff Accountant

Plano, TX · On-site

$70K - $90K/yr

Experience in biotech, pharma, or another early-stage/start-up environment * NetSuite experience ... Exposure to AP automation, T&E platforms, forecasting platforms, or contract management systems ...

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of ... Ensure compliance with GCP, SOPs, protocols, and regulatory standards Financial & Contract ...

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Biotech Contract Manager information

What is a biotech contract manager?

A Biotech Contract Manager oversees contracts related to biotechnology partnerships, vendors, research agreements, and regulatory compliance. They negotiate terms, ensure adherence to legal and industry standards, and mitigate risks for their organization. Their role requires collaboration with legal teams, procurement, and scientific departments to support business objectives. Effective contract management helps biotech companies streamline operations, maintain compliance, and optimize financial and operational outcomes.

What are the typical day-to-day responsibilities of a biotech contract manager?

As a Biotech Contract Manager, your daily tasks often include drafting, reviewing, and negotiating a variety of contracts such as research agreements, vendor contracts, and licensing deals. You will regularly collaborate with legal, procurement, research, and finance teams to ensure terms align with company goals and regulatory requirements. Managing timelines, tracking key deliverables, and monitoring compliance throughout the contract lifecycle are also core parts of the role. This position requires balancing multiple priorities and maintaining strong communication with both internal teams and external partners to support the company’s scientific and commercial objectives.

What are the key skills and qualifications needed to thrive as a biotech contract manager?

A Biotech Contract Manager should possess a strong background in contract law, negotiation, and life sciences, often supported by a bachelor's or master's degree in a related field and relevant experience in biotech or pharmaceutical contract management. Familiarity with contract management software, compliance platforms (such as Icertis or DocuSign), and regulatory guidelines like FDA and GxP is highly beneficial. Superior attention to detail, analytical thinking, and excellent interpersonal and communication skills set outstanding professionals apart in this role. These capabilities ensure accurate and efficient contract execution, risk mitigation, and effective collaboration with internal and external stakeholders in a highly regulated industry.

What are popular job titles related to Biotech Contract Manager jobs in Texas?

For Biotech Contract Manager jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Biotech Contract Manager jobs in Texas look for?

The top searched job categories for Biotech Contract Manager jobs in Texas are:

What cities in Texas are hiring for Biotech Contract Manager jobs?

Cities in Texas with the most Biotech Contract Manager job openings:

Infographic showing various Biotech Contract Manager job openings in Texas as of August 2026, with employment types broken down into 89% Full Time, 10% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution.

Experienced Contract Manager

Medpace, Inc.

Irving, TX • On-site, Remote

$82K - $110K/yr

Full-time

Medical, Retirement, PTO

Re-posted 14 days ago


Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 74 rated research


Job description

Job Summary

We are growing rapidly, and currently seeking a full-time,office-based Site Contract Manager to join our Clinical Operations team in our Dallas, TX office. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you! 

Responsibilities
  • Serve as the primary contact for internal colleagues and external clients regarding clinical trial contract life cycle management and progression of site-level negotiations
  • Lead the review, negotiation, and finalization of terms and conditions for clinical trial contracts and investigator grant budgets
  • Identify, evaluate, and mitigate operational, legal, and financial risks associated with clinical trial contract negotiations
  • Provide mentorship and guidance to contract specialists and junior managers
Qualifications
  • Bachelor's degree in a related field of study;
  • 3+ years of contract drafting, redlining, and negotiation experience
  • Experience with clinical trial contracting or life sciences commercial operation

Travel: minimal 

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events 

Please note benefits may vary based on country. 

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Employment Type: OTHER

What Medpace employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Medpace logo

About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992