Part-Time Dermatologist/ Principal Investigator
Methuen, Massachusetts
Employer: System One Holdings, LLC
Industry:
Salary: Competitive
Job type: Part-Time
Title: Principle Investigator - Part-Time Dermatologist
Location: Methuen, MA
Type: Contract
Start Date: ASAP
One of the largest and fastest-growing Clinical Research site networks is seeking a part-time (1-2 days/week) Dermatologist to work onsite in their Methuen, MA site. If you want to be a part of this groundbreaking work, please apply!
The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.
Essential Job Duties:
Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role; Experience in a medical research environment is preferred. Board certification in area of specialty highly preferred.
Required Skills:
Location: Methuen, MA
Type: Contract
Start Date: ASAP
One of the largest and fastest-growing Clinical Research site networks is seeking a part-time (1-2 days/week) Dermatologist to work onsite in their Methuen, MA site. If you want to be a part of this groundbreaking work, please apply!
The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.
Essential Job Duties:
- Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes
- Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance
- Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
- Participates and engages in successful delivery and retention of study participants.
- Interacts positively and collaboratively with sponsors, clients and team members.
- Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.
- Actively involved in protocol training for staff.
- Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.
- Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.
Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role; Experience in a medical research environment is preferred. Board certification in area of specialty highly preferred.
Required Skills:
- Clinical skills and procedures based on area of specialty.
- Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).
- Must possess strong organizational skills, attention to detail, and math proficiency.
- Well-developed written and verbal communication skills. Bi-lingual (English / Spanish) proficiency is highly preferred.
- Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers.
- Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
Created: 2024-06-26
Reference: 321879
Country: United States
State: Massachusetts
City: Methuen