Clinical Trial Associate

Join our team in a dynamic hybrid role, offering flexibility to work remotely and from our headquarters in Watertown, MA.

COMPANY OVERVIEW:

Disc Medicine is a clinical-stage biopharmaceutical company committed to discovering, developing, and commercializing novel treatments for patients who suffer from serious hematologic diseases. We are building a portfolio of innovative, first-in-class therapeutic candidates that aim to address a wide spectrum of hematologic diseases by targeting fundamental biological pathways of red blood cell biology, specifically heme biosynthesis and iron homeostasis. Disc Medicine values collaboration, professional development, and scientific integrity and promotes an inclusive company culture that empowers and inspires.

POSITION OVERVIEW:

Disc Medicine is hiring a new XXX due to the fast growth of the company's portfolio. The successful candidate will serve as the XXX. Reporting to tXX, this position will have visibility to the development teams and executive leadership with meaningful opportunities for professional development and career growth.

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.
  
  

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.
  
  

The annual base salary range for this position is listed below. Actual pay rates are determined by considering multiple factors including qualifications, relevance of experience, education & credentials, subject matter expertise, and internal parity.

Salary Range

$73,100—$98,900 USD

Disc Medicine is an equal-opportunity employer committed to providing all qualified candidates and employees equal opportunities. We offer comprehensive benefits and competitive compensation packages. The Company headquarters are in Watertown, MA, and we provide a flexible work environment.

Disc Medicine actively recruits individuals with an entrepreneurial spirit and a drive for excellence. Interested candidates should submit a cover letter and resume to be considered for current and future opportunities.