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Cystic Fibrosis Remote Jobs (NOW HIRING)

Cystic Fibrosis Remote information

What is the difference between Cystic Fibrosis Remote vs Pulmonologist?

AspectCystic Fibrosis RemotePulmonologist
CredentialsMedical degree, CF-specific training, licensureMedical degree, pulmonology fellowship, licensure
Work EnvironmentRemote, telehealth platforms, patient consultationsHospitals, clinics, private practices, outpatient settings
Industry UsageHealthcare, telemedicine, patient supportHealthcare, specialized respiratory care

While both roles require medical credentials and focus on respiratory health, Cystic Fibrosis Remote professionals primarily provide telehealth services for CF patients, whereas Pulmonologists work in clinical settings diagnosing and treating respiratory conditions. The remote role offers flexibility and virtual patient interaction, while Pulmonologists often work directly with patients in healthcare facilities.

What are common challenges faced when working remotely as a Cystic Fibrosis care coordinator, and how can they be addressed?

Remote Cystic Fibrosis care coordinators often face challenges such as maintaining effective communication with patients and multidisciplinary teams, managing confidential health information securely, and ensuring timely follow-ups. To address these issues, coordinators typically use secure telehealth platforms, schedule regular virtual check-ins, and collaborate closely with physicians, nurses, and social workers. Being proactive about patient outreach and utilizing digital health tools helps maintain high-quality care and supports positive patient outcomes.

What is a Cystic Fibrosis Remote position?

A Cystic Fibrosis Remote position typically refers to a job in the healthcare field that supports individuals with cystic fibrosis (CF) through remote means, such as telehealth, virtual patient monitoring, or administrative support. These roles can include remote CF care coordinators, telemedicine nurses, or researchers who work off-site to provide patient education, care coordination, and support services. Remote positions allow professionals to assist CF patients and families while minimizing in-person contact, which is especially important due to the vulnerability of CF patients to infections.

What are the key skills and qualifications needed to thrive as a Cystic Fibrosis Remote Care Coordinator, and why are they important?

To thrive as a Cystic Fibrosis Remote Care Coordinator, you need a background in nursing or respiratory therapy, experience with chronic disease management, and relevant licensure or certification. Familiarity with telehealth platforms, electronic medical records (EMR), and remote monitoring tools is typically required. Excellent communication, empathy, and organizational skills help build trust with patients and ensure effective care coordination. These abilities are crucial for delivering high-quality, patient-centered support to individuals with cystic fibrosis in a remote setting.
More about Cystic Fibrosis Remote jobs
What cities are hiring for Cystic Fibrosis Remote jobs? Cities with the most Cystic Fibrosis Remote job openings:
What are the most commonly searched types of Cystic Fibrosis jobs? The most popular types of Cystic Fibrosis jobs are:
What states have the most Cystic Fibrosis Remote jobs? States with the most job openings for Cystic Fibrosis Remote jobs include:
Infographic showing various Cystic Fibrosis Remote job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.
Clinical Supply Specialist (Contract)

$58 - $70/hr

Full-time

Posted 25 days ago


Job description

Attention recruitment agencies: All agency inquiries are vetted through 4DMT's internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.
4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company's lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company's lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company's second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery
GENERAL SUMMARY:
Reporting to the Director, Supply Chain, this role is expected to work closely within the Supply Chain team, as well as cross-functional groups such as Clinical Operations and Quality.
This is a remote or hybrid position.
RESPONSIBILITIES:
  • Supports the development and execution of Clinical Supply strategies for all 4DMT's Phase 1/2/3 investigational drug products and ancillaries
  • Coordinate and track bulk drug orders to ensure adherence to pre-defined supply and resupply timelines
  • Monitor site inventory on a daily basis; coordinate and and track drug shipments to ensure uninterrupted supply
  • Supports drug product inventory management and distribution in partnership with 4DMT's clinical partners; evaluates drug utilization versus forecast considering country requirements and logistical timeline
  • Maintains study and depot-level accountability and reconciliation documentation to support regulatory compliance and study closeout
  • Tracks and resolves study and depot level temperature excursions. Provide routine reporting of drug wastage due to these excursions
  • Archives Proof of Delivery (POD) documentation
  • Maintain traceable documentation to support GXP activities
  • Archives documentation on Trial Master Files as required

QUALIFICATIONS:
Education and Experience:
  • Degree in biological or life sciences, pharmacy or medicine (or international equivalent). A minimum of 3 years in the pharmaceutical industry or relevant work experience and a minimum of 1 year in Clinical Supply Chain.
  • Familiar in the daily management and operations of a Clinical Supply Chain inclusive of bulk management, distribution, and maintaining study blinds across multiple investigational products
  • Experienced with Interactive Response Technology - IRT systems for inventory management and resupply
  • Working knowledge of regulations relating to clinical labeling, packaging, and distribution activities; working knowledge of GMP/GCP/GLP regulations

Skills:
  • Intermediate/Advanced knowledge of Microsoft Suites
  • Knowledge of Clinical Supply Management
  • Solid written and verbal communication skills
  • Excellent planning and organizational skills and the ability to work simultaneously on multiple projects with tight timelines
  • Excellent interpersonal and communication skills
  • Positive attitude with a strong desire for continuous learning

Hourly compensation range: $58.00 - 70.00
4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities