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Associate Director, Clinical Business Operations

BioSpace

Waltham (MA)

On-site

USD 130,000 - 200,000

Full time

3 days ago
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Job summary

BioSpace is seeking an Associate Director for Clinical Business Operations in Waltham, MA. This key role focuses on clinical vendor outsourcing, budget management, and ensuring compliance with regulatory requirements. Candidates should have significant experience in the pharmaceutical or biotech industries and demonstrate leadership skills to foster team collaboration and operational efficiencies.

Qualifications

  • At least 8 years of experience in a pharmaceutical/biotech.
  • Experience in outsourcing management and negotiations.
  • Able to manage a large volume of work in a dynamic environment.

Responsibilities

  • Lead the operational aspects of clinical business operations.
  • Develop strategic plans for clinical trials.
  • Manage vendor relationships and contract negotiations.

Skills

Leadership
Project Management
Communication
Analytical Skills
Negotiation Skills

Education

Bachelor's degree; advanced degree preferred

Job description

Associate Director, Clinical Business Operations

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Associate Director, Clinical Business Operations

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Company Overview

Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leveraging the modularity of its FORCE platform, Dyne is developing targeted therapeutics that deliver to muscle and the central nervous system (CNS). Dyne has a broad pipeline for neuromuscular diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD) and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.

Company Overview

Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leveraging the modularity of its FORCE platform, Dyne is developing targeted therapeutics that deliver to muscle and the central nervous system (CNS). Dyne has a broad pipeline for neuromuscular diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD) and preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.

Role Summary

The Associate Director, Clinical Business Operations provides support for clinical vendor outsourcing and financial oversight, tracking and forecasting for Dyne’s clinical trials. This role is responsible for leading vendor identification and selection efforts in support of Dyne’s Clinical trials ensuring cross functional input and evaluation. Work to optimize and ensure efficient spend within Clinical Operations. The Associate Director, Clinical Business Operations works closely with cross functional teams to ensure a fit-for-purpose outsourcing strategy and budget management is achieved for each trial. This role will work closely with other internal stakeholders including Finance, Legal and Quality.

This role is based in Waltham, MA without the possibility of being a remote role.

Primary Responsibilities Include

  • Lead and manage the operational aspects of clinical business operations, including overseeing clinical trial budgets, vendor selection and relationship management
  • Develop and implement strategic plans to optimize clinical business operations and ensure the efficient and cost-effective execution of clinical trials
  • Collaborate with cross-functional teams, including clinical development, regulatory affairs, and finance, to align on trial execution plans and milestones
  • Manage relationships with external vendors, CROs, and other partners to ensure high-quality deliverables, adherence to timelines, and budget management
  • Assist in the development and management of clinical trial budgets, forecasting and expenses
  • Ensure compliance with regulatory requirements, GCP guidelines, and company SOPs in all aspects of clinical business operations
  • Provide leadership and mentorship to team members, fostering a culture of collaboration, continuous improvement, and excellence in clinical business operations
  • Provide support of the Request for Information (RFI) and/or Proposal (RFP) process for Development programs and/or clinical studies of various phases, complexity, and risk
  • Manage contract and financial negotiations with external service providers for Development programs
  • Partner with the Legal to ensure that the appropriate templates and legal terms/conditions are applied
  • Maintain current knowledge of outsourcing industry trends and provide ongoing support and training to key stakeholders on best outsourcing practices
  • Proactively identify and collaborate to address opportunities for process or business improvements including operational efficiencies
  • Embrace and enable diversity of perspectives to enhance the overall effectiveness of the team
  • Represent Clinical Operations and support other functions on company-wide process improvements and initiatives
  • Travel up to 25% domestic and/or international


Education And Skills Requirements

  • Bachelor's degree; advanced degree (e.g., MBA, MPH) preferred
  • At least 8 years of experience working within a pharmaceutical/biotech company, CRO, or similar organization
  • Demonstrated leadership and project management skills, with a track record of successfully leading cross-functional teams and delivering results on time and within budget
  • Excellent communication and interpersonal skills, with the ability to effectively collaborate and establish effective business relationships with internal and external stakeholders at all levels
  • Experience in outsourcing management, vendor budget negotiations, budget management, and vendor oversight
  • Experience in developing and implementing process improvements and operational efficiencies in clinical business operations
  • Experience as a strategic partner providing effective and complex solutions and systems to the organization
  • Comprehensive understanding of clinical trial operations regulatory requirements, with an understanding of clinical trial operations
  • Strong analytical, negotiating and business communication skills.
  • Ability to think strategically and effectively communicate ideas
  • Able to interact and influence effectively with multi-functional teams at all levels of the organization
  • Self-motivated and able to prioritize and manage a large volume of work in a dynamic, changing, growing start-up culture


The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.

This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned. All Employees are expected to adhere to all company policies and act as a role model for company values.

Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

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