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Radformation

Clinical Affairs Specialist - Physicist / Dosimetrist

RemoteUnited States onlyArchived
Published
Experience
Senior
Employment
Full-time
Company size
Startup
$120k–$190k/yr
Check eligibility

Open to US only. Set where you work from to check your eligibility.

No BS summary

Clinical Affairs Specialist with 3+ years of Radiation Oncology clinic experience (medical physicist, assistant, or dosimetrist) needed for strategy development, process improvement, regulatory submissions, and product support. Must be highly motivated, analytical, passionate about learning, and possess strong communication and strategic thinking skills.

Core skills

clinical affairsregulatory affairs

Required skills

ISO 13485GSPR(s)

Optional skills

ISO 13485PRISMA Model

Required languages

English

What you'll do

  • Assist in the preparation of regulatory submissions and impact assessments.
  • Perform clinical evaluation plans and reports
  • Perform literature searches and reviews
  • Work with regulatory agencies and partners worldwide to achieve market access and compliance.
  • Comply with the quality management system and ISO 13485.
  • Ensure compliance with regulations.
  • Explain regulations, policies, or procedures.
  • Provide technical review of data and reports.
  • Coordinate clinical documentation activities.
  • Update Clinical Evaluation Reports on an annual basis.
  • Document Compliance with GSPR(s)
  • Update Annual Post-Market Surveillance Reports

What they require

  • 3+ years of Radiation Oncology clinic experience as a medical physicist, medical physics assistant, or dosimetrist
  • Ability to research journals, papers, and publications to identify current state of the art as it relates to external beam radiation oncology applications and procedures.
  • Ability to write research reports for independent review.
  • Experience with test protocols and clinical evaluations
  • Highly motivated
  • Strong analytical skills
  • Passionate about learning
  • Excellent communication and interpersonal skills
  • The ability to think strategically, multitask, and meet deadlines
  • Preferred Experience: 3+ years of clinical affairs experience performing clinical evaluation reports
  • Experience with Quality Management Systems and ISO 13485
  • Experience writing CEPs and CER’s for EU-MDR Submissions
  • Familiar with PRISMA Model

Benefits

  • Competitive salary
  • Immediate Health/Vision/Dental insurance
  • Generous Paid Time Off
  • Multiple high-quality medical plan options with substantial employer contributions toward premiums, often covering the full cost depending on the plan selected.
  • Health coverage starting on day one
  • Short-term and long-term disability and supplementary life insurance
  • 401(k) with employer match vested immediately
  • Annual reimbursement for professional memberships
  • Conference attendance and continued learning opportunities
  • Self-managed PTO and 10 paid holidays
  • Monthly internet stipend
  • Company-issued laptop and one-time home office setup stipend
  • Fully remote work environment with virtual events and yearly retreats, because we like to have fun while doing work that matters
  • For teammates outside the US, we provide benefits that align with local laws and standards, working with our Employer of Record (EOR) partners to ensure fairness and equity. This means your benefits package will be locally compliant, competitive, and designed to support your health, financial security, and work-life balance.

Healthcare Technology

HealthcareStartup
$120k–$190k/yr