If you are a passionate clinical professional seeking a meaningful opportunity in the biotech industry, this Clinical Research Associate job at a rare disease‑focused biotech company in Massachusetts might be your next big move. The role gives you the chance to contribute directly to cutting‑edge clinical trials, working with patients, investigators, and internal teams to help bring therapies for rare diseases to life.
About the Company
The hiring organization is an emerging biotech firm located in Massachusetts, focused on rare and ultra‑rare disease research. With a mission to deliver innovative treatments for patient populations with high unmet medical needs, this rare‑disease biotech firm is committed to excellence, scientific rigor, and patient‑centric development. The company cultivates a collaborative culture, combining clinical trial operations, regulatory strategy, and translational science to bring forward impactful therapies. Clinical Research Associate job in USA.
As a prospective member of their clinical operations team, you’ll be working in a dynamic and fast‑paced environment, supporting trial execution from site initiation through close‑out and helping ensure high quality, compliance and efficiency in the rare disease space.
Role Overview: Clinical Research Associate Job
In this Clinical Research Associate job, you will play a key role in managing and overseeing clinical trial sites, ensuring adherence to protocol, regulatory standards and patient safety. Your work will be central to the successful execution of studies that may shape the future of therapies for rare disease patients. Clinical Research Associate job in USA.
Key Responsibilities:
- Monitor clinical trial sites to ensure compliance with study protocol, GCP (Good Clinical Practice), and regulatory requirements.
- Support site initiation visits, routine monitoring visits, and close‑out visits, particularly in rare disease indications.
- Document site performance, data integrity, and safety reporting with precision and attention to detail.
- Collaborate with cross‑functional teams, including Project Management, Data Management, and Regulatory Affairs, to maintain trial timelines and site quality.
- Assist in training site staff, supporting documentation of informed consent, and reviewing source data against case report forms (CRFs).
- Contribute to trial risk assessments, site escalation plans, and process improvements tailored to rare disease trials.
Key Requirements:
- Bachelor’s degree in life sciences, nursing, or a related field; advanced degree preferred but not required.
- 2‑5 years of experience as a CRA or similar role in clinical operations, ideally in biotech or rare disease settings.
- Familiarity with GCP, FDA/EMA regulatory frameworks, and clinical trial monitoring procedures.
- Excellent written and verbal communication skills, strong attention to detail, and ability to work independently in a dynamic environment.
- Ability to travel domestically as required to clinical trial sites in the U.S. Experience with rare disease trials is a plus.
Salary & Benefits
For this Clinical Research Associate job, the compensation, and benefits reflect the specialized setting of rare disease clinical research in Massachusetts.
- Expected Salary Range: USD 70,000 – 90,000 annually, depending on experience and role scope.
Benefits Include:
- Comprehensive health, dental and vision insurance plans.
- Generous paid time off (vacation, sick leave) plus holidays.
- 401(k) retirement plan with company match.
- Professional development support including opportunities to attend conferences and obtain certifications in clinical research.
- Collaborative and rewarding work environment focused on rare disease impact and patient‑centric trial design.
- Potential for future career growth into senior clinical operations or project management roles within the biotech sector.
How to Apply
Ready to launch your career in rare disease clinical research? Submit your application via the company’s careers portal:
👉 Apply Here: Current Opportunities—Ultragenyx
Please include your current CV, a cover letter that emphasizes your experience in clinical monitoring or operations (especially in trial settings) and highlights any exposure to rare disease studies or biotech environments. Show your commitment to quality, patient safety and trial execution excellence.
Conclusion
This Clinical Research Associate job with a rare disease biotech firm in Massachusetts presents an exciting career path for those who want to combine clinical expertise with a mission‑driven environment. By contributing to trials that target unmet needs and rare patient populations, you’ll be part of a team making a real difference. If you’re ready for an engaging role in clinical operations and rare disease research, this opportunity invites you to step into a meaningful and growth‑oriented position. Don’t miss the chance—apply today and help drive innovation in patient care. Clinical Research Associate job in USA.
FAQ
1. What experience is required?
You should have 2‑5 years of clinical research monitoring or operations experience, preferably in biotech or clinical trials.
2. Will this role involve travel?
Yes—the position may require domestic travel to clinical trial sites in the U.S., depending on the study design and locations.
3. Is rare disease experience mandatory?
Not strictly mandatory, but experience in rare disease trials or biotech settings is a strong plus and will enhance your application.
4. What salary range is expected?
Typically between USD 70,000 and 90,000 annually for this CRA role within a rare disease biotech firm in Massachusetts.
5. How do I apply?
Visit the careers portal via Ultragenyx’s Current Opportunities link (see above) and submit your CV, cover letter, and relevant trial experience.
