- Great opportunity to get into clinical research for the first time or continue a career with an organization 100% focused on bettering the clinical trial process
- More consistent and stable work schedule and environment
- Laid back environment compared to the hustle and bustle of a typical hospital setting
- Attends Site Initiation Visits (SIV), Pre-Selections Visits (PSV), and Investigators meetings as required.
- Participates in recruitment initiatives and strategy development to ensure targets are achieved; ensuring recruiting studies enroll according to plan within timelines and targets.
- Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants.
- Interprets protocols and IB.
- Manages and reviews IVRS, CRF/EDC, if applicable.
- Oversees management of investigational medical products (IMP).
- Identifies and reports trends within studies to manage them in light of conduct and outcome.
- Oversees multiple studies and/or studies with higher numbers.
- Cares for and protects the safety of participants through ethical conduct, this should receive the highest priority at all times during all aspects of the study
- Fulfills and complies with all medical duties, ensuring that clinical trials are performed to acceptable medical, scientific, and ethical standards and meet the requirements as per protocol, SOP/COP ICH, and local GCP guidelines and regulations.
- Ability to relocate or commute to be ON-SITE in DeLand, FL clinic
- A valid medical degree with at least 3 years of working as a licensed physician
- Valid registration as a medical practitioner and in good standing and with unrestricted ability to practice in place of work
Primary Care Physician - DeLand, United States - Sqrl
Description
OPPORTUNITY IN DELAND, FL
Clinical Research Physician (Principal Investigator) ON-SITE in DeLand with a fast-growing clinical research organization
Must be a certified MD in the state of Florida
HIGHLIGHTS
DAY TO DAY
This role will provide you oversight responsibilities over many different trials covering a variety of disease states, including cutting-edge research trials. These responsibilities include the execution of the clinical study protocol, the delegation of responsibilities to other site operations staff, ensuring compliance standards are met, and general oversight of the progress of studies.
Responsibilities:
Carries out clinical evaluation and assessment of participants to ensure eligible participants are recruited and monitored for safety and adherence.
Must Haves: