Scientist

ZRG Careers; United States; Remote; USD 68,880 - 82,656; Full time

Job summary

A specialized healthcare firm is seeking a Scientist to support precision medicine programs. Responsibilities include clinical data evaluation, patient assessment, and collaboration with healthcare teams. Ideal candidates will possess a doctorate and demonstrate strong analytical and communication skills. This remote position requires adherence to quality standards and active participation in patient advocacy, ensuring best practices in treatment strategies and data management.

Qualifications

• Doctorate in a clinically relevant area is mandatory.
• Collaborative and effective communication skills are essential.
• Strong analytical skills and problem-solving capabilities required.

Responsibilities

• Conduct comprehensive assessments of participant data.
• Collaborate to create and deliver treatment strategies to patients.
• Review diagnostic testing options and help navigators.

Skills

Excellent communication and interpersonal skills

Strong analytical and problem-solving capabilities

Knowledge of medical ontologies and/or experience with medical claims

Understanding of precision medicine principles

Ability to focus on process improvement

Education

Doctorate in a clinically relevant area of study

Job description

Base Pay Range

$50.00/hr - $60.00/hr

Scientist Location: US Remote

Reports to: Sr. Director, Scientific Services

Function: Clinical

About the Role

As a Scientist, you will be crucial in aligning patients and treatments as part of our precision medicine programs. Your responsibilities will include patient identification review, clinical data evaluation, research on existing and developmental treatments for various diseases, and helping to develop and test alignment algorithms. This role is 100% remote.

Key Responsibilities

• You will work both independently and collaboratively to support our navigators, senior scientists, and clinicians in the following areas:
• • Patient Assessment: Conduct comprehensive assessments of participant data to confirm eligibility and potential benefits from precision medicine programs.
  • Treatment Strategies: Collaborate with other scientists, clinicians, and navigators to create and deliver treatment strategies (reports) to patients and physicians as a report.
  • Navigators and Patient Education: Communicate with navigators and other care team members to answer scientific questions and ensure a proper understanding of precision medicine and treatment strategies (including benefits, risks, and expectations).
  • Diagnostic Test Support: Review diagnostic testing options and results and assist navigators in understanding the indications for and implications of diagnostic testing. Create disease and patient‑specific diagnostic strategies.
  • Clinical Trials: Review and curate clinical trials and research studies for eligible patients.
  • Data Management: Review and maintain accurate and confidential patient records, including genetic and clinical data (ensuring compliance with privacy regulations).
  • Patient Advocacy: Advocate for patient needs, preferences, and concerns to ensure their voice is heard in the healthcare decision‑making process.
  • Quality Assurance: Ensure that precision medicine services meet the highest quality standards and adhere to industry regulations.

Qualifications

• Doctorate in a clinically relevant area of study.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with multidisciplinary teams.
• Strong analytical and problem‑solving capabilities.
• Knowledge of medical ontologies and/or experience with medical claims is preferred.
• A strong understanding of precision medicine principles, genetic testing, and genomic data interpretation is also preferred.
• Keen ability to focus on process improvement.

Success Metrics

• Zero critical errors in treatment strategy or report content leading to misalignment with patient eligibility. ≥ 95% of reports meet internal peer‑review and quality assurance standards on first submission.
• Average turnaround time ≤ 7 business days from receipt of complete patient data to delivery of final treatment strategy report.
• ≥ 90% of assigned patient cases completed within target timelines while maintaining quality.
• ≥ 95% of documentation updates (e.g., diagnostic recommendations, test reviews) completed within required timeframes.
• Response time ≤ 24 hours for navigator or clinician scientific inquiries.
• Active participation in interdisciplinary case discussions, contributing actionable insights in ≥ 90% of relevant reviews.

About Medzown

Medzown is transforming the way patients with cancer and other complex or rare diseases access life‑changing treatments. Our mission‑driven platform combines deep clinical expertise, advanced technology, and data science to deliver personalized treatment strategies—including clinical trials—to help patients find the right treatment at the right time. We don’t just guide patients—we advocate for them every step of the way. Join us in shaping the future of precision medicine and making a real difference in people’s lives.

Medzown is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based on race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran under applicable federal, state, and local laws. All qualified applicants will be considered for employment without regard to these or any other characteristics protected by law.