Clinical Research Coordinator at MIT spin-off medical device startup - Boston, MA

Only for registered members Boston, MA , United States

1 day ago

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Clinical Research Coordinator · The Position · You will serve as the on-site Clinical Research Coordinator (CRC) supporting the execution of a study at a partner hospital site. · This is a full-time, on-site role embedded within the anesthesia department. You will work directly a ...
Job description

Clinical Research Coordinator

The Position

You will serve as the on-site Clinical Research Coordinator (CRC) supporting the execution of a study at a partner hospital site.

This is a full-time, on-site role embedded within the anesthesia department. You will work directly alongside Certified Registered Nurse Anesthetists (CRNAs) and anesthesiologists throughout their daily case load, serving as the primary on-site data collector and operational point of contact for the study.

This role reports to the Principal Investigator (PI) and works closely with the PASCALL Systems clinical research team.

The Key Responsibilities of This Role Are:

On-Site Data Collection & Case Coverage

  • Be present on-site at the study hospital for full operating room days during the anticipated study period
  • Observe clinical workflow during surgical cases and collect protocol-required data in real time
  • Record case milestones and identify any protocol deviations
  • Coordinate scheduling with operating room and anesthesia staff to ensure consistent study coverage

Other Responsibilities Include:

Device & Data Systems Management

  • Troubleshoot basic device or connectivity issues and escalate to the PASCALL technical team as needed
  • Maintain organized records for each enrolled case, including case logs and data quality notes

Protocol Adherence & Regulatory Support

  • Maintain thorough knowledge of the study protocol, including eligibility criteria, data collection windows, and phase-specific procedures
  • Maintain regulatory binders and administrative files in accordance with ICH GCP guidelines
  • Identify, document, and promptly communicate protocol deviations to the PI and study team

Coordination & Communication

  • Participate in regular study team check-ins
  • Communicate operational challenges, scheduling conflicts, or data gaps promptly
  • Support overall study execution and operational excellence

About PASCALL SYSTEMS:

  • Sustainably grown startup with an FDA-510(k)-cleared medical device
  • Founding team includes: a MIT PhD Neuroscience graduate as CEO, a joint MIT/Harvard professor, statistician, and anesthesiologist at MGH, and a former Harvard, currently Stanford professor, in Anesthesiology and Bioengineering. Both professors run their own laboratories and key opinion leaders in their field. The founding team has strong ties with both MIT and Harvard.

Problem we are working on: to bring neuroscience-based personalized anesthesia monitoring to the operating room (OR). PASCALL founders also have strong ties to the anesthesia department at Massachusetts General Hospital through Drs. Brown and Purdon's work, allowing our team to remain connected with current problems in the field.

Our mission is to revolutionize anesthesia care by advancing the field into an era of neuroscience-based personalized care. Our vision is to bring personalized, innovative, and strong science-based anesthesia care to all hospitals in the world and in doing so prevent post-operative delirium and post-operative cognitive dysfunction.

Since our founding, PASCALL has built significant capabilities in the development of medical devices and software. We achieved ISO13485:2016 certification for the design and development of medical devices. Our first platform device was FDA cleared in 2022.

Our team is a diverse and international group, bringing together a range of expertise and unique perspectives. Alongside advanced degrees in algorithm development, machine learning, pharmacy, and anesthesiology, we also have members with backgrounds in fields as varied as music and history.

The ideal candidate should be:

  • Curious and quick learner
  • Highly effective organizer
  • A clear and effective communicator both in writing and verbally
  • Meticulous with attention to detail
  • Skilled in identifying and solving unseen problems
  • Have an interest to learn about/develop a career in healthcare, especially roles in clinical studies/planning
  • Currently a senior in their last semester/new graduates with 1–2 years of working experience

Educational Background

  • Current minimum GPA of at least 3.5/4 or 4.6/5
  • Degree or exposure to Biomedical/Biomedical Engineering/Health Sciences/Public Health preferred

Experience

  • Prior experience/exposure in clinical study, administrative or management roles

Benefits:

  • Dental insurance (full time employees only)
  • Health insurance (full time employees only)
  • 12 Paid time off days for full time employees
  • Professional development assistance

Application Requirement: Application not addressing ALL 5 questions in the cover letter won't be considered

  • What excites you about this job?
  • Where do you see yourself in 5 years, and how would this team help you achieve your 5-year plan?
  • Provide examples of how you meet each key qualification in the job description
  • List any questions you have about this job
  • List any concerns you have about this job

Job Types:

Full-time, Contract, Internship, Part-time

Pay:

Full-time

$55,799 - $69,469 per hour

Internship/Part-time

$ $33.00 per hour

Schedule:

Monday to Friday

Ability to Commute:

Boston, MA Required)

Ability to Relocate:

Boston, MA 02114: Relocate before starting work (Required)

Work Location:

Hybrid

Job Types: Full-time, Temporary

Pay: $55, $69,469.00 per year

Ability to Commute:

  • Boston, MA Required)

Ability to Relocate:

  • Boston, MA 02114: Relocate before starting work (Required)

Work Location: In person



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