Locums – Boston, Massachusetts, Fully Remote - Physician Clinical Trial Sub-Investigator Job
Boynton Beach, Florida, United States
Job Summary
Occupation
Physician
Specialty
Internal Medicine
Degree Required
MD/DO
Position Type
Locums/Travel
Work Environment
Hospital
Clinic/Private Practice
Location
Boston, Massachusetts, United States
Visa Sponsorship
No
Job Description
Last Update:
1/06/25
Locums – Boston, Massachusetts, Fully Remote – Physician Clinical Trial Sub-Investigator
Clinical Role:
- Do you know someone that might be a good fit for this position? Please ask about our generous referral fees!
- Start Date: 2/3/25
- A clinical-stage biopharmaceutical company translating insights from genetic epilepsies into the development of therapies for CNS disorders characterized by neuronal excitation-inhibition imbalance
- Work location details: Fully remote
- Specialty needed: Physician Clinical Trial Sub-Investigator (also called Sub-I’s)
- All Physician specialties eligible, pediatric neurology preferred
- Number of providers needed: 1-2
- Study is set to begin in the first quarter of 2025
- 6 months+ for initial efficacy with the option to extend into the Long-Term Safety Study (LTSS)
- This trial will go on for another 18+ months, with the opportunity to work on additional trials in the future
- The provider should be able to offer a minimum of 20+ hours per week, in 3+hr blocks, consistently
- They will be asked to provide their specific availability through Outlook, and this will be used as the main scheduling tool for the patients to meet with the physician
- M - F between the hours of 8am – 6pm
- Evening and weekend blocks accepted on a case per case basis
- ** Providers (also called “Sub’I’s) will be aligned with a patient and will follow the visit schedule for the trial and throughout the patient's journey as part of the study. They will be tasked with:
- Determining subject eligibility
- Document visit findings and relay to the PI in accordance with agreed procedures
- Reviewing Columbia Suicide Severity Rating Scale (C-SSRS) assessments
- Overseeing of Adverse Event (AE) Relatedness / Severity Assessments
- Deciding on the Discontinuation of Trial Treatment/Emergency unblinding treatment.
- Overseeing Clinical Reports (ECG, Central Lab Testing)
- Conducting and recording Video Neurological Examination assessment for Eligibility Review Committee submission
- Performing protocol eCOA efficacy and safety assessments (TETRA S-ADL, CGI-S, C-SSRS, oversee participant PGI-S, PGI-C)
- Assessing Physical Exam results
- Reviewing Lab Results for Clinical Significance
- Interpretating above reports and reporting their findings
- Signing Case Report Forms
- Board Certification within the Physician Scope of Practice
- Clinical trial experience as a Sub-Investigator
- ACTIVE GCP certification (Good Clinical Practice)
- Designed to give the researcher a basic understanding of the regulations and requirements for research using investigational (not approved by FDA) drugs or devices
- 20+ ACTIVE state licenses - no exceptions
- Priority is for the states of Massachusetts and Virginia
- IMLC Accepted (Provide LOQ)
- Allow RecruitWell to set up a phone call with you and the client to discuss more!