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Edgewise Therapeutics

Develops therapies for rare muscular disorders

Senior Manager - Medical Affairs Operations

Business OperationsConfirmed live in the last 24 hours
Full-timeUnited StatesIn-person

About the Job

Requirements

  • A bachelor's degree in business, life sciences, healthcare, or a related field, or an equivalent combination of education and relevant experience.
  • At least 5 years of experience in pharmaceutical or biotechnology operations, Medical Affairs operations, program or project management, or a related function.
  • Demonstrated experience with budget tracking, forecasting, purchase orders, invoices, accruals, contracts, and vendor-management workflows.
  • Strong project-management and organizational skills, including the ability to independently manage multiple workstreams, deadlines, stakeholders, and changing priorities.
  • Working knowledge of pharmaceutical industry compliance requirements and operational processes involving healthcare professionals, vendors, and medical materials.
  • Excellent written and verbal communication skills and the demonstrated ability to influence and drive follow-through without direct authority.
  • High proficiency with Microsoft Office and collaborative project-management and reporting tools.

Responsibilities

  • Maintain an integrated view of Medical Affairs priorities, tactics, milestones, dependencies, and decisions across Medical Strategy, Scientific Communications, Medical Directors, and Field Medical.
  • Develop and maintain project plans, calendars, trackers, action logs, and risk registers for key Medical Affairs initiatives; follow through with owners and escalate risks or resource constraints appropriately.
  • Coordinate annual and long-range Medical Affairs planning, including collecting functional inputs, consolidating tactical plans, managing timelines, and preparing leadership updates.
  • Establish and support Medical Affairs operating routines, including leadership meetings, planning sessions, cross-functional reviews, and periodic business updates.
  • Develop dashboards and reports showing activity status, budget performance, operational risks, and key milestones.
  • Coordinate the Medical Affairs budgeting process and track forecasts, commitments, actuals, accruals, and variances with Medical Affairs leadership and Finance.
  • Manage operational workflows for purchase orders, invoices, vendor setup, statements of work, contract routing, renewals, and closeout; resolve delays and discrepancies.
  • Maintain a centralized view of Medical Affairs vendors, agreements, deliverables, and spend, and support vendor performance reviews and resource-planning decisions.
  • Coordinate healthcare professional contracting, fair market value assessments, payment documentation, and related compliance requirements with Legal, Compliance, Finance, and designated medical owners.
  • Lead operational coordination for Medical Affairs congress activities, including master timelines, registrations, travel and meeting logistics, vendor coordination, internal planning, and post-congress reconciliation.
  • Provide end-to-end operational support for advisory boards and other external medical meetings, including contracting, attendee logistics, venue and vendor coordination, material routing, documentation, payments, and closeout.
  • Coordinate internal Medical Affairs meetings and planning sessions, including scheduling, agendas, pre-reads, action capture, decision documentation, and follow-up.
  • Partner with scientific and medical owners to ensure operational readiness while leaving scientific objectives, agendas, content, and external relationships with the appropriate Medical Affairs leads.
  • Coordinate Medical Affairs content-review workflows, including submission preparation, routing, status tracking, metadata, approval documentation, expiration, withdrawal, and archiving; substantive medical and compliance review remains with designated reviewers.
  • Maintain organized, audit-ready repositories for Medical Affairs plans, approved materials, meeting documentation, contracts, standard operating procedures, work instructions, and governance records.
  • Serve as an operational point of contact for relevant Medical Affairs systems and tools, coordinating user access, onboarding, training, issue resolution, and continuous improvement with system owners and IT.
  • Support fit-for-stage Medical Information operations as needed, including intake and inquiry tracking, approved-response library administration, documentation, and escalation workflows, while scientific response ownership remains with the designated medical lead.
  • Develop, document, and improve Medical Affairs processes, standard operating procedures, templates, and working practices to increase consistency, efficiency, compliance, and scalability.
  • Coordinate operational onboarding and offboarding for Medical Affairs team members, including systems access, shared resources, required training, and team-process orientation.
  • Provide administrative and operational support to Medical Affairs leadership and the broader organization, anticipating needs and ensuring timely follow-through.
  • Serve as an operational liaison with Finance, Procurement, Legal, Compliance, IT, Clinical Development, Regulatory, Commercial Operations, and other relevant partners.
  • Identify operational bottlenecks and implement practical solutions that improve clarity, accountability, and execution without adding unnecessary process burden.
  • Promote a collaborative, service-oriented, and continuous-improvement mindset across Medical Affairs operations.

Desired Qualifications

  • Experience working in a small or mid-sized biotechnology company or another fast-paced, evolving environment.
  • Hands-on experience with Veeva Vault and/or Veeva CRM, Smartsheet, Power BI, or comparable content, project-management, and reporting platforms.
  • Experience coordinating congresses, advisory boards, external expert contracting, and Medical Affairs content-review workflows.
  • Experience developing standard operating procedures, work instructions, dashboards, templates, and scalable operational processes.
  • Project-management certification or formal project-management training.

About the Company

Edgewise Therapeutics

Develops therapies for rare muscular disorders

Edgewise Therapeutics develops therapies for rare muscle disorders using a proprietary drug discovery platform. Its lead molecule, sevasemten (EDG 5506), targets the muscle motor protein myosin to reduce stress in fast skeletal muscle fibers, aiming to improve muscle health without affecting other muscle types. The company owns global development and commercialization rights to its programs and pursues strategic collaborations and asset acquisitions to accelerate its pipeline. Its focus is precision medicine for conditions like Duchenne muscular dystrophy, Becker muscular dystrophy, Limb Girdle muscular dystrophies, and McArdle disease. Overall, Edgewise seeks to deliver targeted treatments that protect and improve muscle health for patients and families affected by these rare diseases.

Company size
51-200
Company stage
IPO
Headquarters
Boulder, CO
Founded
2017

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