Disc Medicine

👥 51-100💰 $225,500,000 Post-IPO Equity about 1 month agoPharmaceuticalBiotechnologyTherapeuticsMedicalHealth 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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📍 United States

🧭 Full-Time

🔍 Biopharmaceutical

  • Bachelor’s degree in Human Resources or related field
  • 2-4 years of HR experience
  • Proficiency in Greenhouse and Microsoft Office Suite
  • Strong organizational and multitasking skills
  • Provide administrative support across HR functions
  • Manage recruitment process including job postings and interviews
  • Assist with HR data management and reporting
  • Collaborate on projects to improve employee experience

Microsoft Office SuiteRecruitment

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📍 United States, Canada

🧭 Full-Time

🔍 Biopharmaceutical

  • Bachelor's degree in scientific discipline or equivalent experience
  • Minimum of 3 years in pharmaceutical industry experience in Quality Assurance
  • Strong team player with communication skills
  • Attention to detail and information processing skills
  • Knowledge in Microsoft Word, Adobe, Excel, Smartsheet
  • Knowledge of GxP regulations preferred
  • Experience with EDMS and EQMS preferred
  • Manage GxP Documents and training assignments
  • Foster Quality mindset around Good Documentation Practices
  • Lead routine activities for Document Change Requests and Training
  • Track and present metrics to Leadership
  • Assist with GxP electronic system validation
  • Assist with QMS and process improvements

Microsoft ExcelAttention to detailQuality Assurance

Posted 10 days ago
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📍 United States, Canada

🧭 Full-Time

🔍 Biopharmaceutical

  • BS or equivalent in a scientific discipline with 10+ years of experience
  • Advanced degree with 7+ years of experience in the pharmaceutical industry
  • Extensive knowledge of FDA, EU, ICH regulations
  • Exceptional organizational and communication skills
  • Develop and implement quality standards and procedures for GCP/GVP/GLP
  • Lead and conduct internal and external audits
  • Manage audit responses and track CAPAs
  • Provide training on current regulations and compliance issues
  • Represent Quality in project teams

GCPComplianceTrainingQuality AssuranceRisk Management

Posted 10 days ago
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🔥 Clinical Trial Manager
Posted 10 days ago

🔍 Biopharmaceutical

  • BA/BS required
  • Advanced skills in Microsoft Office programs as well as good working knowledge of electronic data systems
  • 5+ years of applicable clinical trial experience (2-5 years of vendor and CRO management) required
  • Thorough knowledge of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies globally
  • Must be willing to travel both domestic and international
  • Strong interpersonal skills to interact with investigators, vendors, and individuals at all levels of the organization
  • Experience working on project teams is required
  • Strong business acumen: including in-depth knowledge of the multidisciplinary functions involved in a company’s drug development process, e.g., data management, biostatistics, regulatory, pharmacovigilance, etc. and can proactively integrate multiple perspectives into the clinical development process for best end-results.
  • Supports the clinical team in the overall management of studies, including planning, execution and closeout of one or more clinical trials in accordance with clinical development plans/strategy and timelines
  • Assist with the evaluation, selection, and oversight of CROs, external vendors and consultants to ensure successful clinical trial implementation and execution
  • Contribute to the writing and review of clinical documents such as protocols, informed consent forms, investigator brochures, trial reports, ASRs/DSURs, and trial status updates
  • Review and approve study-related operational plans generated by CROs and vendors, and ensure the documentation is in accordance with GCP regulatory requirements and consistent with the protocol for assigned studies
  • Ensure audit-ready condition of clinical trial documentation including the trial master file
  • Review and provide input on clinical monitoring visit reports and ensure that all outstanding follow-up items are closed out in a timely manner
  • Ensures risks are proactively identified, managed, and mitigation strategies implemented
  • Liaise with clinical site staff and Investigators as appropriate to ensure optimal Sponsor-site relationships
  • Assist with planning and conduct of investigators’ meetings
  • Assist with monitoring progress of clinical study activities and report on the progress of assigned clinical trials including budget and timelines
  • May perform periodic visits to sites and/or CROs to assess progress of studies/protocol compliance
  • Participate in the preparation and review of SOPs
  • Attend and provide support in meeting scheduling and distribution of meeting agendas/minutes
  • Perform any other business need identified by their direct line Manager.
Posted 10 days ago
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📍 United States, Canada

🧭 Full-Time

🔍 Biopharmaceutical

  • Bachelor’s degree
  • 2–4 years of administrative experience
  • Excellent written and verbal communication skills
  • Proficiency in Microsoft Office Suite
  • Strong organizational and time-management abilities
  • Keen attention to detail
  • Provide direct administrative assistance to key leaders
  • Schedule and manage calendars for executives
  • Arrange travel logistics
  • Order and maintain office supplies and inventory
  • Greet visitors and handle meeting setups
  • Assist in organizing corporate events
  • Collaborate with HR on branded swag inventory
  • Support leadership and various departments as needed

Communication SkillsAttention to detailOrganizational skillsTime ManagementMicrosoft Office Suite

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