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Remote Biotech Contract Manager Jobs in Delaware

Study Contracts Manager

Wilmington, DE · On-site +1

$112K - $168K/yr

Ensure final contract documents are consistent with agreements reached at negotiations. * Ensure ... Desirable Skills/Experience: * Ability to work in an environment of remote collaborators.

This role is based in United State and is a remote position. You will be part of a collaborative ... industrial biotechnology environment (enzymes, food, fuel alcohol, or similar) * 3-5 years of ...

The Care Manager (RN/SW) assists members appropriate for care management and care coordination ... Those fully remote associates residing in states where service is required by contract, law, or ...

The Care Manager (RN/SW) assists members appropriate for care management and care coordination ... Those fully remote associates residing in states where service is required by contract, law, or ...

The Care Manager (RN/SW) assists members appropriate for care management and care coordination ... Those fully remote associates residing in states where service is required by contract, law, or ...

The Care Manager (RN/SW) assists members appropriate for care management and care coordination ... Those fully remote associates residing in states where service is required by contract, law, or ...

... and biotechnology? At Radiometer, one of Danaher's 15+ operating companies, our work saves lives ... Sales Manager and is part of the Blood Gas Sales Team and will be remote, responsible for a ...

Those fully remote associates residing in states where service is required by contract, law, or ... We offer integrated managed care products, pharmaceutical benefit management and specialty pharmacy ...

BioPharma Business Developer

Wilmington, DE · On-site +1

$132K - $198K/yr

... remote depending on business needs. Compensation: The current salary range for this role is ... Build, manage, and strengthen long-term relationships with key BioPharma customers, distributors ...

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Remote Biotech Contract Manager information

What is a remote biotech contract manager?

A Remote Biotech Contract Manager is a professional who oversees and manages contracts related to biotechnology projects, products, or services while working remotely. Their duties include drafting, reviewing, negotiating, and ensuring compliance with legal and regulatory requirements for contracts between biotech companies and partners, vendors, or clients. They serve as a liaison between legal, procurement, and project teams to ensure that agreements align with business objectives and industry standards. By working remotely, they utilize digital tools to collaborate and maintain documentation efficiently. This role is vital in minimizing risk and supporting the successful execution of biotech initiatives.

How does a remote biotech contract manager typically collaborate with legal, research, and procurement teams while working offsite?

As a Remote Biotech Contract Manager, collaboration with cross-functional teams is usually achieved through regular virtual meetings, project management tools, and shared document platforms. You’ll work closely with legal teams to ensure contract compliance, partner with research departments to clarify technical requirements, and coordinate with procurement to streamline vendor agreements. Strong communication skills and proficiency with digital collaboration tools are essential for aligning all parties and keeping contracting processes efficient. Despite being remote, you’ll often be expected to provide timely updates, facilitate negotiations, and address any contract-related issues as they arise.

What are the key skills and qualifications needed to thrive as a remote biotech contract manager, and why are they important?

To excel as a Remote Biotech Contract Manager, you need expertise in contract negotiation, knowledge of regulatory compliance in biotechnology, and experience with legal documentation, often supported by a degree in law, business, or life sciences. Familiarity with contract management software, e-signature platforms, and regulatory databases is typically required. Strong attention to detail, effective communication, and the ability to manage multiple priorities remotely are standout soft skills for this role. These abilities are crucial for ensuring contracts are legally sound, compliant, and efficiently managed in a highly regulated and dynamic industry.

What is the difference between Remote Biotech Contract Manager vs Remote Biotech Regulatory Affairs Specialist?

AspectRemote Biotech Contract ManagerRemote Biotech Regulatory Affairs Specialist
Required CredentialsBachelor's in Life Sciences, Contract Management CertificationBachelor's in Life Sciences, Regulatory Affairs Certification
Work EnvironmentContract negotiations, vendor management, legal complianceRegulatory submissions, compliance monitoring, agency communication
Employer & Industry UsagePharmaceutical companies, biotech firms, CROsPharmaceutical companies, biotech firms, regulatory agencies
Common Search & ComparisonYesYes

The Remote Biotech Contract Manager primarily handles contract negotiations, vendor relationships, and legal compliance within biotech and pharma companies. In contrast, the Remote Biotech Regulatory Affairs Specialist focuses on regulatory submissions, compliance with industry standards, and communication with regulatory agencies. While both roles require a background in life sciences and industry-specific certifications, their core responsibilities and work environments differ significantly.

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

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

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

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

What cities in Delaware are hiring for Remote Biotech Contract Manager jobs?

Cities in Delaware with the most Remote Biotech Contract Manager job openings:

Infographic showing various Remote Biotech Contract Manager job openings in Delaware as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution.

Study Contracts Manager

Wilmington, DE • On-site, Remote


AstraZeneca
Pharmaceutical Product Wholesalers • 10K+ employees

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

People enjoy working here

Good employer

Recommended by students


$112K - $168K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Job description

Study Contracts Manager
Introduction to role:
Are you ready to play a pivotal role in the world of clinical trials? As a Study Contracts Manager, you'll be at the forefront of negotiating and budgeting, ensuring ethical and compliant practices in developing and managing contracts with investigators, institutions, and external vendors. Your expertise will drive costings and contracts, making a significant impact on the success of clinical studies. Regular communication with key stakeholders will be your forte as you navigate the complexities of clinical trial agreements. This position serves as a flexible contracting and budgeting resource, providing coverage across studies and teams based on business needs, workload balancing, and organizational priorities.
Accountabilities:
  • Adapt global templates of agreements to local use in accordance with local requirements and SOPs.

  • Develop and negotiate clinical site budgets based on Fair Market Value.

  • Negotiate agreement language and budget with clinical study sites.

  • Act as point of contact and interface with Legal if necessary to ensure integrity of contracts.

  • Maintain the status of agreements, budgets, issues, payments, amendments, and communications for the duration of the study.

  • Ensure final contract documents are consistent with agreements reached at negotiations.

  • Ensure all agreements are executed in a timely manner, contributing to efficient site start-up timelines.

  • Support internal and external audit activities.

  • Ensure compliance with AstraZeneca's Code of Conduct and company policies and procedures relating to people, finance, technology, and security.

  • Ensure that all contracts are included in the TMF.

  • Additional responsibilities may include training and mentoring new members of the local Study Team regarding financial/contractual issues and sharing experiences, supporting preparation and negotiation of a Local Master Service Agreement, and contributing to process improvements, knowledge transfer, and best practice sharing.

Essential Skills/Experience:
  • Bachelor's degree required in related discipline with 4+ years of experience negotiating industry contracts such as Clinical Study Agreements, CDAs, and amendments for site, SMO, CRO, or Sponsor.

  • Experience developing clinical trial budgets from study protocols, including Fair Market Value assessments.

  • Ability to support multiple studies and agreement types, adapting quickly to changing business needs and priorities

  • Provide flexible contracting and budgeting support across multiple studies, including negotiation of CSAs, CDAs, amendments, and budgets creation

  • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.

  • Good knowledge of relevant local regulations.

  • Basic understanding of the drug development process.

  • Good understanding of Clinical Study Management including monitoring, study drug handling and data management.

  • Excellent attention to detail.

  • Good written and verbal communication skills.

  • Good collaboration and interpersonal skills.

  • Good negotiation skills.

Desirable Skills/Experience:
  • Ability to work in an environment of remote collaborators.

  • Demonstrated ability to rapidly learn new studies and support contracting and budgeting needs with minimal training or oversight.

  • Post-graduate training in contracts administration or work experience as a paralegal in pharmaceutical or health care industry.

  • Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business.

  • Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.

  • Good analytical and problem-solving skills.

  • Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.

  • Familiar with risk-based monitoring approach including remote monitoring.

  • Good cultural awareness.

  • Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.

  • Team oriented and flexible.

At AstraZeneca, we are driven by our passion for science and innovation. Our commitment to exploring new frontiers in healthcare allows us to make a significant impact on patients' lives worldwide. We embrace curiosity and courage, empowering our teams to make bold decisions that lead to groundbreaking discoveries. With a collaborative environment that unites diverse expertise from academia, biotechs, and industry, we are dedicated to delivering life-changing medicines. Join us in our mission to redefine what's possible through science.
Ready to make a difference? Apply today and be part of our journey towards transforming healthcare!
The annual base pay for this position ranges from $112,154 to $168,232. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
20-Aug-2026
Closing Date
28-Aug-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB


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