Clinical Site Budgets Manager
Clinical Site Budgets Manager

Clinical Site Budgets Manager

Boston Full-Time Home office possible
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At a Glance

  • Tasks: Manage clinical site budgets and oversee investigator payments for groundbreaking medical trials.
  • Company: Join Blueprint Medicines, a leader in biopharmaceutical innovation.
  • Benefits: Enjoy competitive pay, health benefits, and a supportive remote work environment.
  • Why this job: Make a real difference in patients' lives while advancing your career in a dynamic field.
  • Qualifications: Bachelor’s degree and 3+ years in budget management for clinical trials required.
  • Other info: Be part of a diverse team that values creativity and collaboration.

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Join to apply for the Clinical Site Budgets Manager role at Blueprint Medicines

This range is provided by Blueprint Medicines. Your actual pay will be based on your skills and experience β€” talk with your recruiter to learn more.

Base pay range

$60.00/hr – $60.00/hr

Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solving important medical problems in two core focus areas: allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a proven track record of success with two approved medicines, including bringing our medicine to patients with systemic mastocytosis (SM) in the U.S. and Europe. Leveraging our established research, development, and commercial capability and infrastructure, we now aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases including SM and chronic urticaria, breast cancer and other solid tumors.

Job Title: Clinical Site Budgets Manager

Location: Remote (EST Hours)

Job Description

How will your role help us transform hope into reality?

This position reports into the Senior Manager Clinical Site Budgets. The right candidate will possess an understanding of Investigator Grant Management activities for successful execution of multiple clinical trials primarily in oncology, allergy and hematology indications in various phases of development.

Responsibilities of this position involve the day-to-day management of overseeing the CROs development of investigator payments, reviewing investigator grant budgets and developing parameters for negotiations for the CRO. Will act as an escalation point for the CRO and the investigator when budgets fall out the acceptable range.

What will you do?

  • Review investigator budgets against the schedule of events within the protocol
  • Identify research related costs versus Standard of Care costs and support teams in site contract negotiations
  • Use Fair Market Value (FMV) benchmarking tools such as Grant Plan and Grants Manager to develop template study site budgets
  • Leads and oversees the overall investigator site payment process with the CROs
  • Establish acceptable negotiation ranges for our CROs to use when working with investigators
  • Serve as an escalation point for the CRO for Investigator Grant Negotiations with sites
  • Act as SME for internal clients regarding FMV costs and investigator reimbursement.
  • Supervises the status of budget negotiation to expected timeline and reviews CRO metrics of performance
  • Identifies and seeks efficiency with our CROs, to ensure improved value for service
  • Participates and could present in Clinical Trial, CRO kick off, Investigator budget financial review and CRO governance meetings

What minimum qualifications do we require?

  • Minimum Education Required: Bachelor’s degree in scientific or business discipline.
  • Previous clinical experience a plus
  • Understanding of the drug development process T
  • The candidate should ideally have 3 + years in investigator budget and contract management with a sponsor company or CRO managing various phase clinical trials.
  • Ability to work with minimal direction
  • Motivated self-starter who can work in a fast-paced environment
  • Creative problem solver with good communication and written skills.
  • Strong interpersonal and organizational skills are needed, with a high degree of attention to detail.
  • Proficient with the MS Office Suite

What additional qualifications will make you a stronger candidate?

  • Resourcefulness/ Flexibility – The ability to adapt to working optimally within a variety of situations; adapts to change and to changes in job demands
  • Communication and Partnership – Ability to optimally express ideas in written and oral context; collaboration, team-building skills and interpersonal skills; genuine desire to be on a team and contribute to organizational and team goals
  • Effective Planning – Demonstrated effective time management skills and execution
  • Perseverance – Pursues tasks with energy, drive and initiative; comfortable in an accountable environment where you can make an impact
  • Problem Solving – Ability to understand a situation or problem by breaking it down into smaller pieces using a detailed approach and to identify patterns and connections between situations that are not obviously related
  • Relationship Building – Builds productive working relationships across a diverse spectrum of people

Pay Transparency

The pay range that Magnit reasonably expects to pay for this position: $55.00-60.00/hour.

Benefits: Medical, Dental, Vision, 401K (provided minimum eligibility hours are met).

Why Blueprint?

At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success.

This is the place where the extraordinary becomes reality, and you could be part of it.

Patients are waiting. Are you ready to make the leap?

Equity, Diversity, Inclusion and Affirmative Action

At Blueprint Medicines, we foster a culture of equity, diversity, and inclusion. A proud Equal Employment Opportunity and Affirmative Action employer, we consider all qualified applicants without regard to race, color, sex, gender identity or expression, sexual orientation, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, or any other characteristic protected under applicable law. We are also an E-Verify Employer. We will make reasonable accommodations, absent undue hardship, for qualified individuals with known disabilities. If you are an individual with a disability in need of accommodation with the application or recruiting process, please reach out to TotalRewards@blueprintmedicines.com.

For more information, please see our EEO-AA Policy Statement, the EEO Know Your Rights Poster, as well as our Pay Transparency Statement.

Seniority level

  • Seniority level

    Not Applicable

Employment type

  • Employment type

    Contract

Job function

  • Job function

    Finance and Sales

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Clinical Site Budgets Manager employer: WillHire

Blueprint Medicines is an exceptional employer, offering a dynamic remote work environment that empowers employees to make a meaningful impact in the biopharmaceutical industry. With a strong focus on equity, diversity, and inclusion, the company fosters a collaborative culture where innovative thinkers can thrive and grow professionally. Employees benefit from competitive compensation, comprehensive health benefits, and the opportunity to contribute to life-changing medicines that alleviate human suffering.
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Contact Detail:

WillHire Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Clinical Site Budgets Manager

✨Tip Number 1

Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. The more people you know, the better your chances of landing that Clinical Site Budgets Manager role.

✨Tip Number 2

Prepare for interviews by researching Blueprint Medicines thoroughly. Understand their mission, values, and recent projects. This will help you tailor your answers and show them you’re genuinely interested in being part of their team.

✨Tip Number 3

Practice your responses to common interview questions, especially those related to budget management and negotiation. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your experience effectively.

✨Tip Number 4

Don’t forget to follow up after your interview! A simple thank-you email can go a long way in showing your appreciation and keeping you top of mind for the hiring team. And remember, apply through our website for the best chance!

We think you need these skills to ace Clinical Site Budgets Manager

Investigator Grant Management
Clinical Trial Budgeting
Negotiation Skills
Fair Market Value (FMV) Benchmarking
CRO Management
Attention to Detail
Communication Skills
Problem-Solving Skills
Organisational Skills
Time Management
Interpersonal Skills
Adaptability
Self-Motivation
Analytical Skills

Some tips for your application 🫑

Tailor Your Application: Make sure to customise your CV and cover letter for the Clinical Site Budgets Manager role. Highlight your relevant experience in investigator budget management and any specific skills that match the job description. We want to see how you can bring value to our team!

Showcase Your Skills: Don’t just list your qualifications; demonstrate how your skills align with what we’re looking for. If you’ve got experience with FMV benchmarking tools or managing CROs, make it pop! We love seeing real examples of your problem-solving abilities.

Be Clear and Concise: When writing your application, keep it straightforward. Use clear language and avoid jargon unless it’s relevant. We appreciate a well-structured application that gets straight to the pointβ€”this shows us you can communicate effectively!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it gives you a chance to explore more about us and what we stand for at Blueprint Medicines!

How to prepare for a job interview at WillHire

✨Know Your Numbers

As a Clinical Site Budgets Manager, you'll be dealing with budgets and financial metrics. Brush up on your understanding of Fair Market Value (FMV) and how to use benchmarking tools like Grant Plan and Grants Manager. Being able to discuss these confidently will show that you’re prepared and knowledgeable.

✨Understand the Protocol

Familiarise yourself with the clinical trial protocols relevant to oncology, allergy, and hematology. Knowing the ins and outs of the schedule of events will help you identify research-related costs versus standard care costs, which is crucial for budget negotiations.

✨Showcase Your Problem-Solving Skills

Be ready to discuss specific examples where you've tackled challenges in budget management or negotiations. Highlight your creative problem-solving abilities and how they’ve led to successful outcomes in previous roles. This will demonstrate your fit for a fast-paced environment.

✨Build Rapport

Since this role involves collaboration with CROs and investigators, practice building rapport during your interview. Show your interpersonal skills by engaging with the interviewer and expressing genuine interest in teamwork and partnership. This will reflect your ability to foster productive working relationships.

Clinical Site Budgets Manager
WillHire

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