Disc Medicine

👥 51-100💰 $225,500,000 Post-IPO Equity 2 months agoPharmaceutical Biotechnology Therapeutics Medical Health Care📈 Public Company

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Disc Medicine is a clinical-stage biopharmaceutical company at the forefront of hematologic disease treatment. We are dedicated to discovering, developing, and commercializing novel therapies for patients with severe hematologic disorders, with our pipeline focused on innovative treatments like bitopertin. Our commitment lies in targeting fundamental biological pathways and developing first-in-class therapeutic candidates. Our tech stack supports our mission with platforms like Drupal, Akamai EdgeWorkers, and Adobe Dynamic Tag Management. We leverage technologies like HSTS, Google Maps, and mobile optimization to ensure our digital infrastructure is robust and accessible. Our engineering culture is collaborative, and we value scientific integrity. We are growing rapidly and committed to technological innovation to advance our research and development efforts. We are a publicly traded company with strong financial backing and a focus on attracting talented professionals. We offer a hybrid work environment, and our Watertown, MA, headquarters provides a collaborative setting. At Disc Medicine, we foster an inclusive company culture that promotes professional development and empowers our employees. We're seeking individuals with an entrepreneurial spirit and a drive for excellence to join our team and help us make a difference in patients' lives.

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Jobs at this company:

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🔥 Clinical Trial Associate

Posted 7 days ago

🔍 Biopharmaceutical

🔧 Requirements

BA/BS required
Understanding of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies globally
Strong knowledge of MS Word, Excel, PowerPoint, and Outlook
Ability to effectively collaborate with both internal and external study team
Ability to take initiative and ownership of new activities as they arise
Ability to work in a fast-paced environment with demonstrated ability to manage multiple competing tasks and demands
Experience working on project teams is required
Candidate should be a self-driven individual with skills in organization, building working relationships and communication.

💡 Responsibilities

Provide support for critical day-to-day clinical study activities, including inspection readiness and/or oversight of inspection deliverables and/or milestones, in accordance with established protocols under the general supervision of the CTA Manager.
Collaborate with the Clinical Trial Manager, study teams, vendors, and Clinical Research Organizations (CROs) to support clinical study activities defined by the clinical trial operating model.
Supported the clinical trial manager with preparing and coordinating bi-weekly clinical trial team meetings and finalizing meeting materials such as agendas, slides, and meeting minutes; tracked and followed up on action items.
Development and/or review and approval of study documentation, including essential document packets, study plans, informed consent forms, etc.
Contribute to the writing and review of clinical documents such as protocols, informed consent forms, investigator brochures, trial reports, ASRs/DSURs, laboratory manuals, pharmacy manuals, and trial status updates.
Ensure audit-ready condition of clinical trial documentation, including the trial master file, and leading internal TMF quality reviews with cross-functional team members on the study-defined cadence.
Track patient samples and reconcile sample discrepancies with sites and applicable central labs; coordinate sample movement and data deliverables on time with business needs and accompanying data deliverable timelines.
Assist the finance department with invoices, clinical projections, and per-patient cost estimates.
Work closely with the CRO to support study and site start-up activities such as SIV slide development, process flows, contract and budget negotiations, site ICF customizations, assist with answering site IRB questions, etc., to ensure start-up occurs within an established timeline.s
Review and provide input on clinical monitoring visit reports and ensure that all outstanding follow-up items are closed out in a timely manner.
Collaborate with internal departments (Legal, Finance, Nonclinical, etc.), CROs, and external vendors.
Establish and maintain trial-related processes/systems with study vendors such as central labs, clinical supplies, IP depot, and CRO as assigned per protocol requirements.
Help develop and drive timelines and collaborate with cross-functional teams to align on deliverables to help support data cuts, conference needs, interim analyses, etc.
Monitor the progress of clinical study activities and report on the progress of assigned clinical trials, including budget and timelines.
Oversee the updating and maintenance of patient trackers to accurately reflect all enrolled, screened, and screen-failed patients within the study. Ensure timely completion of patient visits and proactively follow up with sites and CROs regarding any outstanding visits. Provide real-time patient updates to the Clinical Trial Team as needed
Initiate clinicaltrials.gov updates and publications based on business needs and other study updates.
Participate in the preparation and review of SOPs.
Perform any other business need identified by their direct line Manager.

Posted 7 days ago

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🔥 Senior Director, Patient Marketing and Digital Innovation

Posted 10 days ago

🔍 Life sciences

🔧 Requirements

Bachelor’s Degree required; MBA or another Advanced Degree preferred
Minimum of 12 years in life sciences, including significant experience in the marketing function
Extensive working knowledge of strategic and brand marketing and omnichannel approaches
Experience defining the strategy for a brand or portfolio of products with multiple indications
Ability to oversee the generation of insights and apply those insights to business issues and opportunities
Analytical mindset, with demonstrated ability to develop strategy, make strategic recommendations, monitor performance, understand ROI and allocate resources
Ability to thrive in a fast-paced, start-up environment with a hands-on approach
Proven track record of successfully leading product launches, globally and in the US
Strong preference given to candidates with hematology and rare disease experience
Strong project management skills, with the ability to spearhead launch teams
Excellent communication and interpersonal skills, with the ability to collaborate effectively across teams and departments

💡 Responsibilities

Become the expert in the patient journey via insight generation; educate the cross-functional team as needed and drive strategic choices by identifying unique leverage points within the journey
Lead the development and implementation of tactical marketing plans to create a differentiated brand experience, through personal and non-personal promotion, that drives patient engagement and rapid product uptake
Maintain a high degree of external focus with significant customer and field team engagement
Lead execution of omni-channel HCP & Patient/Caregiver tactical plans
Partner with Digital Marketing Lead
Seek out and implement innovative digital solutions in the development of our direct to patient strategy and overall digital efforts to engage and educate patients
Lead strategic exploration and development of innovative patient identification and adherence efforts
Work with cross-functional team to develop the patient/caregiver brand narrative and ensure alignment with overall brand narrative and strategy
Partner with cross-functional team, especially Patient Advocacy, Patient Services and HCP Marketing, to collectively plan and develop a flawless patient experience
Establish the patient ambassador program and ensure alignment with cross-functional team
Develop strong working partnerships with cross-functional team including Medical, Patient Services, Patient Advocacy, Program Management, Commercial Operations, Legal, Regulatory, IT and external agencies
Oversee the direction and deliverables of multiple priorities ensuring internal stakeholder alignment, across agency partners, and cross functional partners
Manage the patient marketing budget, ensuring efficient allocation of resources
Establish clear objectives and key performance indicators (KPIs) to measure the success of marketing plan implementation
Contribute to an efficient and compliant medical and legal review process
Act in full compliance with all laws, regulations and policies

Posted 10 days ago

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🔥 Associate Director, Program Management

Posted 12 days ago

📍 Massachusetts

🔍 Biotechnology

🔧 Requirements

BS/MS in a scientific-related field.
At least 10 years in the pharmaceutical/biotechnology industry.
At least 5 years of meaningful experience in program management supporting drug development programs (level commensurate with experience).
PMP/PgMP certification (PMI) preferred.
Exceptional communication, presentation, and interpersonal skills, time/resource management, attention to detail, and proven success working in matrixed, highly collaborative environments.
Demonstrated ability to lead a cross-functional team and influence at all organizational levels.
Ability to thrive in a fast-paced, innovative, and, at times, uncertain or changing environment while remaining flexible, proactive, and resourceful.
Proven track record prioritizing and managing multiple tasks simultaneously, integrating cross-functional issues, and balancing competing priorities effectively.
Demonstrated competence in independently navigating and synthesizing complex information in a fluid environment.
Proficiency in MS Office (including Word, PowerPoint, Excel, and Project).

💡 Responsibilities

Partner closely with PL to drive the development and execution of strategic, integrated program team goals.
Effectively communicate with cross-functional program team members, Executive Team members, and key stakeholders on program status, objectives, risks, and mitigation plans.
Identify appropriate presentation topics and coordinate preparation and program team alignment with compelling presentation materials for governance meetings.
Ensure cross-functional reporting and presentation of relevant information to the program team and other key stakeholders.
Facilitate decision-making, collaboration, and problem-solving with people at all levels of the organization to accomplish program team goals.
Identify program bottlenecks and issues. Proactively drive for their resolution.
Recognize, track, and monitor key program assumptions, milestones, and decision points to drive the delivery of program objectives.
Facilitate team meetings using program management best practices and tools to drive cross-functional communication, timely and effective decision-making and conflict resolution, and successfully execute project objectives.
Develop and maintain a risk registry with the Portfolio and Program Management team, including detailed risk assessments, mitigations, and resolutions.
Identify process improvement opportunities and develop and implement solutions.
Apply experience and lessons learned to manage program team dynamics and performance.
Partner with Finance to develop budgets/forecasts/long-range plans for assigned program(s).
Mentor/coach junior colleagues to drive professional growth.

Project ManagementCross-functional Team LeadershipCommunication SkillsMicrosoft ExcelAgile methodologiesMentoringOrganizational skillsTime ManagementMS OfficeRisk ManagementStakeholder managementBudget managementPowerPoint

Posted 12 days ago

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🔥 Director, Commercial Data Operations & Reporting

Posted 16 days ago

🔍 Biopharma

🔧 Requirements

12+ years of relevant experience in biopharma commercial data operations, forecasting, or analytics, with increasing leadership responsibilities. Experience in a pre-commercial biotech or pharmaceutical launch environment.
Experience overseeing commercial data strategy, reporting, and vendor relationships.
Expertise in commercial data integration, MDM, data governance, and analytics tools to drive business insights.
Demonstrated project and stakeholder management skills with a track record of leading cross-functional initiatives.
Hands-on experience with SQL, SAS, Python, or other data manipulation tools for commercial data analysis.
Ability to partner with commercial leadership, sales operations, and finance teams to define KPIs and enhance reporting.
Proven experience managing specialty pharmacy data and third-party data providers for commercial operations.
Strong understanding of data quality management, commercial data lakes, and incentive compensation calculations.
Experience in business process optimization, system enhancements, and automation of reporting workflows.
Strong background in rare diseases or specialty pharmaceuticals preferred.
Familiarity with global data operations and regulatory compliance related to commercial data management.

💡 Responsibilities

Develop, implement, and maintain management and field reporting dashboards to track key commercial metrics.
Partner with internal teams and third-party vendors to support the operations of Master Data Management (MDM), Data Lakes, Data Quality Management (DQM), Catalog, Governance, Analytics, and Commercial Reporting.
Manage data integration from specialty pharmacies and other data providers into the internal commercial data warehouse.
Define, track, and optimize key performance indicators (KPIs) across commercial operations.
Provide data-driven insights and analytical support to business leaders to inform decision-making.
Drive the implementation of system enhancements and reporting improvements in collaboration with business and IT teams.
Serve as the primary liaison between commercial operations, IT, and external data vendors (e.g., CDE provider, MMIT, payer mastering).
Oversee incentive compensation calculations and ensure accurate data processing.

Posted 16 days ago

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🔥 Senior Accountant

Posted 18 days ago

🔍 Biotech

🔧 Requirements

A bachelor’s degree in accounting is required, and a minimum of 3-5 years in corporate and/or public accounting is required.
Relevant experience in the biotech or pharmaceutical industry, including international experience, is preferred.
Prior experience with NetSuite and Concur is highly preferred.
Strong communication, attention to detail, and ability to work on multiple projects under tight deadlines.
Strong understanding of accounting principles, GAAP
Experience with a publicly traded company, specifically within a SOX 404(b) environment, is required.
Ability to work both independently and deliver responsibilities within a highly collaborative environment.

💡 Responsibilities

Responsible for the cash reconciliation process, including posting intercompany cash transactions to ensure proper recording.
Maintain the fixed asset, prepaids and other current assets and liabilities accounts and reconciliations within FloQast reconciliation software.
Reconcile investment activity on a quarterly basis and perform pricing validation.
Assist in the completion of the accrual process and collaborate with external vendors and internal business stakeholders.
Review and process employee expense reports to ensure compliance with Company policies.
Support the preparation for the financial statement audits and tax compliance reporting.
Support implementation and maintenance of internal controls in accordance with SOX 404(b), including identifying process improvements and operational efficiencies.
Ad hoc projects as needed

Posted 18 days ago

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🔥 Executive Director, Biologics Drug Product

Posted 20 days ago

🧭 Full-Time

🔍 Biopharmaceutical

🔧 Requirements

B.S. degree is required. Advanced scientific degree Ph.D. in a related field is highly preferred.
15+ years of operations experience in the pharmaceutical/biopharmaceutical industry with a minimum of 12 years of leadership experience in leading antibody drug product development teams.
Demonstrated broad knowledge in sterile drug product development, technology transfer, and manufacturing
Prior experience in formulation development of antibody products through various stages of the product lifecycle, including first in human and commercial formulations
Experience in IND and BLA filings is highly preferred
Strong ability to communicate well with cross-functional groups, including Drug Substance, Analytical Development, Quality, Regulatory, and Program Management
Demonstrated ability in managing a department and associated budget
Substantial experience working in CMC teams – with CMC leaders and related team leaders. Preferred to have experience as a CMC leader
Strong network and prior experience with antibody drug product CDMOs
Ability to provide excellent leadership to develop high-performing teams, including exceptional communication and one-team spirit
Excellent collaboration and interpersonal skills; Ability to convey complex ideas succinctly
20-30% travel required

💡 Responsibilities

Lead the drug product function for biologics programs at Disc Medicine
Oversee drug product manufacturing at contract development and manufacturing organizations (CDMO)s
Lead commercial formulation development for antibodies
Engage in selecting appropriate external providers, including formulation and fill/finish process development.
Provide expertise in various areas of biologics drug product, such as in-use compatibility studies.
As appropriate, engage in drug product transfer from one site to another
Provide leadership in performing successful drug product process performance qualifications
Manage a team of individuals and build the function that is poised for growth along with the rest of the company
Form effective relationships and collaborate well with the CMC leader and CMC functions, including drug substance, analytical development, quality control, supply chain, and quality and regulatory organizations.
Responsible for budget management
Engage with Executive Leadership as appropriate to proactively identify technical risks and provide scientific recommendations for mitigation
Foster a positive workplace culture that prioritizes collaboration, ensures accountability, and a commitment to continuous improvement.

Posted 20 days ago

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🔥 Senior/Executive Director, Biotransformation and Drug-Drug Interaction

Posted about 2 months ago

📍 United States, Canada

🧭 Full-Time

🔍 Biopharmaceutical

🔧 Requirements