Associate Director, Clinical Site Budgets and Contracts
Associate Director, Clinical Site Budgets and Contracts

Associate Director, Clinical Site Budgets and Contracts

London Full-Time 54000 - 84000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead site contracts and budgets for groundbreaking mRNA clinical trials.
  • Company: Join Moderna, a leader in mRNA technology transforming global health.
  • Benefits: Enjoy quality healthcare, lifestyle spending accounts, and generous paid time off.
  • Why this job: Make a real impact on patients' lives while collaborating with top professionals.
  • Qualifications: 7+ years in clinical site agreements; strong project management and negotiation skills required.
  • Other info: Embrace a hybrid work model fostering innovation and teamwork.

The predicted salary is between 54000 - 84000 £ per year.

The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that’s revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you’ll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide contributing to global health initiatives. Moderna’s commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients’ lives worldwide.

Moderna is solidifying its presence in London, a global hub for scientific research and innovation. Our London office focuses on commercial operations ensuring the delivery of our revolutionary products to the UK market. We’re seeking talents who are ready to contribute to our mission and transform the landscape of health worldwide.

Reporting to the Director, Business Analytics & Operations Management, the Associate Director, Site Contracts & Budgets will lead the development and negotiation of strategic site business models across the UK and EU. This role involves the execution of global clinical site contracts, spanning Moderna’s clinical trial portfolio, which includes Therapeutics, Oncology, and Infectious Disease. You’ll collaborate closely with internal stakeholders (Clinical Operations, Legal, and Clinical Compliance) and external partners, including CROs and investigator sites, to ensure timely contract execution. In this fast-paced environment, effective communication and the ability to influence stakeholders will be key to your success.

Here’s What You’ll Do:

Your key responsibilities will be:

  • Develop, review, and negotiate investigator site budgets while balancing risks and maintaining clinical trial timelines.
  • Negotiate costs, business terms, and conditions directly with clinical trial sites within approved company parameters.
  • Collaborate cross-functionally to drive value and optimize business models with strategic partners, reducing administrative burdens.
  • Establish tools and processes for developing, negotiating, and tracking global clinical study agreements.
  • Ensure budgets remain within fair market value and monitor actual investigator grant spend against approved budgets.

Your responsibilities will also include:

  • Manage global site budget processes in collaboration with CRO partners.
  • Support Clinical Operations and Finance by providing budget estimates for investigator grants.
  • Oversee site contracting metrics, ensuring system updates and proactive communication of contract statuses and risks.
  • Standardize processes across studies to optimize study budget and start-up timelines.
  • Mitigate challenges in site budget and contract negotiations, resolving escalated issues.
  • Train vendors on Moderna’s templates, tools, and processes, while driving continuous improvement initiatives.

The key Moderna Mindsets you’ll need to succeed in the role:

  • We act with urgency: Your role is crucial in ensuring swift site contracting and budget negotiations, which directly impact the timelines of global clinical trials.
  • We prioritize the platform: By focusing on streamlining global site contracts and partnerships, you will contribute to Moderna’s overarching goal of delivering revolutionary mRNA medicines to market efficiently.

Here’s What You’ll Bring to the Table:

  • BA/BS required; advanced degree preferred. Has knowledge of the principles, concepts, and theories in applicable business discipline.
  • Minimum of 7+ years of direct experience with global, Phase I-IV clinical site agreement and budget negotiations at a biopharmaceutical company and/or CRO required.
  • Experience managing CROs and other vendors performing site budget and contracting activities.
  • Direct experience in the implementation and management of tools and systems to support the operational aspects of site contracts (GrantPlan, GrantManager, etc.).
  • Experience of preparing, negotiating, and finalizing, confidentiality agreements, clinical trial agreements, with direct negotiation with clinical trial sites.
  • Extensive experience managing the preparation and contract negotiation process, including template development, documentation of contract template and revision, approvals, signature process etc.
  • Resolves complex contracts issues.
  • Strong project management, cross-functional team leadership and organizational skills.
  • Outstanding verbal and written communication skills.
  • Ability to manage multiple projects in a fast-paced environment.
  • Ability to collaborate effectively in a dynamic, cross-functional matrix environment.
  • Excellent project management, leadership, communication, management, and organizational skills, as well as a high level of proficiency with problem solving, conflict resolution, negotiation and team building skills.

Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.

We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:

  • Quality healthcare and insurance benefits
  • Lifestyle Spending Accounts to create your own pathway to well-being
  • Free premium access to fitness, nutrition, and mindfulness classes
  • Family planning and adoption benefits
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
  • Educational resources
  • Savings and investments
  • Location-specific perks and extras!

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute and make a meaningful impact.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. We’re focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should

contact the Accommodations and Adjustments team at #J-18808-Ljbffr

Associate Director, Clinical Site Budgets and Contracts employer: Moderna, Inc.

Moderna is an exceptional employer, offering a dynamic work environment in London, a global hub for scientific innovation. With a strong commitment to employee well-being, we provide personalized benefits, generous paid time off, and opportunities for professional growth, all while fostering a culture of collaboration and mentorship. Join us to be part of a pioneering team that is not only transforming medicine but also prioritizing your career development and work-life balance.
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Contact Detail:

Moderna, Inc. Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Associate Director, Clinical Site Budgets and Contracts

✨Tip Number 1

Familiarize yourself with the mRNA technology and its applications in clinical trials. Understanding the science behind Moderna's products will not only help you in interviews but also demonstrate your genuine interest in the company's mission.

✨Tip Number 2

Network with professionals in the biopharmaceutical industry, especially those who have experience in clinical site contracts and budgets. Engaging with current or former employees on platforms like LinkedIn can provide valuable insights and potentially lead to referrals.

✨Tip Number 3

Prepare to discuss specific examples of how you've successfully negotiated contracts and managed budgets in previous roles. Highlighting your direct experience with CROs and your ability to resolve complex contract issues will set you apart from other candidates.

✨Tip Number 4

Stay updated on the latest trends and regulations in clinical trial management and budgeting. Being knowledgeable about industry standards will show that you are proactive and ready to contribute to Moderna's goals from day one.

We think you need these skills to ace Associate Director, Clinical Site Budgets and Contracts

Clinical Site Budget Negotiation
Contract Management
Cross-Functional Collaboration
Project Management
Stakeholder Influence
Risk Assessment
Financial Acumen
Regulatory Compliance
Problem Solving
Communication Skills
Vendor Management
Process Optimization
Confidentiality Agreements
Clinical Trial Agreements
Template Development

Some tips for your application 🫡

Understand the Role: Make sure to thoroughly read the job description for the Associate Director position. Highlight key responsibilities and required skills, and think about how your experience aligns with these aspects.

Tailor Your CV: Customize your CV to reflect relevant experiences that match the job requirements. Emphasize your background in clinical site agreements, budget negotiations, and any experience with CROs.

Craft a Compelling Cover Letter: Write a cover letter that not only showcases your qualifications but also expresses your passion for mRNA technology and its impact on global health. Mention specific examples of past successes in similar roles.

Highlight Soft Skills: In your application, emphasize your communication, negotiation, and project management skills. Provide examples of how you've successfully influenced stakeholders and managed multiple projects in fast-paced environments.

How to prepare for a job interview at Moderna, Inc.

✨Understand the Role and Responsibilities

Make sure you have a clear understanding of the Associate Director position, especially regarding site contracts and budgets. Familiarize yourself with the specific responsibilities mentioned in the job description, such as negotiating investigator site budgets and collaborating with internal stakeholders.

✨Showcase Your Negotiation Skills

Prepare examples from your past experiences where you successfully negotiated contracts or budgets. Highlight your ability to balance risks while maintaining clinical trial timelines, as this is crucial for the role.

✨Demonstrate Cross-Functional Collaboration

Be ready to discuss how you've worked with various teams in previous roles. Emphasize your experience collaborating with Clinical Operations, Legal, and external partners like CROs, as effective communication and influence are key to success in this position.

✨Prepare for Fast-Paced Scenarios

Since the role involves managing multiple projects in a fast-paced environment, think of examples that demonstrate your project management skills and ability to handle challenges. Be prepared to discuss how you prioritize tasks and ensure timely contract execution.

Associate Director, Clinical Site Budgets and Contracts
Moderna, Inc.
M
  • Associate Director, Clinical Site Budgets and Contracts

    London
    Full-Time
    54000 - 84000 £ / year (est.)

    Application deadline: 2027-02-07

  • M

    Moderna, Inc.

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