Clinical Research Physician- Woodstock, GA -Gen Med
Updated 3/16/26
30189, Woodstock, Georgia, United States
Physician
Internal Medicine
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Job at a glance
Degree Required
MD/DO
Position Type
Full-Time
Part-Time/Contract
Work Environment
Outpatient
Visa Sponsorship
No
Job description
Job description
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.
Job Responsibilities
• Provides overall site leadership with a focus on clinical oversight, study performance, enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance.
• 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.
• Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
• Participates and engages in successful delivery and retention of study participants.
• Collaborates with investigators on the study protocols and overall study performance.
• May collaborate with departments leaders in Business Development, Patient Recruitment, Community Outreach, Finance, Budgets and Contracts, and Quality to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), and delivery of quality data to sponsors.
• 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.
• Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.
• Provides training to staff, as needed, on study protocols, assignments and responsibilities.
• Employs strategic thinking and problem-solving skills to propose and implement risk mitigations.
• Participates and presents in management and/or site meetings.
• Perform other duties as assigned, requested, or required based on the needs of the participants, protocols, the site, and/or company.
Qualifications
Working Hours
Skills
Clinical skills and clinical procedures based in 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 effectively handle multiple tasks and adapt to changes in workloads and priorities.
Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.
Must possess a high degree of urgency, self-motivation, integrity and dependability.
Ability to work independently to identify problems and implement solutions.
Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
By applying you agree to our Terms of Service