Description

ClinCept, LLC is seeking a Principal Investigator to utilize their medical expertise in overseeing and directing the clinical course of research participants in clinical trials. This role is crucial for ensuring the medical wellbeing and safety of participants through the proficient execution of studies. Responsibilities include collaborating with the sub investigator, overseeing study protocol adherence, delegating duties to site staff, and ensuring compliance with relevant regulations. This part-time position reports to the President/Chief Executive Officer.

Company Culture and Environment

The company prides itself on a detail-oriented approach that focuses on quality and precision. It fosters a relaxed and positive culture, emphasizing a patient-centric methodology and promoting an excellent work-life balance.

Career Growth and Development Opportunities

As a Principal Investigator, you will have the opportunity to oversee clinical trials and contribute significantly to medical research, potentially leading to further professional development in the field.

Detailed Benefits and Perks

• Flexible schedule
• Competitive salary
• Work remotely possible

Compensation and Benefits

• Pay: Up to $1,000.00 per hour
• Potential earnings from \(0 to \)200,000 a year based on the research budget
• Part-time position with hours less than 20 per week

Why you should apply for this position today

This position offers a unique opportunity to impact clinical research while maintaining an excellent work-life balance. You will be part of a dedicated team that emphasizes patient care and safety.

Skills

• Exceptional understanding of medical terminology, drug safety, and lab report interpretation
• Excellent written, verbal, and presentation skills
• Ability to effectively prioritize and manage multiple projects
• Proficient in Word, Excel, PowerPoint, and Internet navigation

Responsibilities

• Oversee and direct the clinical course of research participants in clinical trials
• Ensure the medical wellbeing and safety of participants
• Collaborate with the sub investigator to execute study protocols
• Delegate study-related duties to site staff
• Ensure site compliance with study protocols and regulations

Qualifications

• Active medical license in good standing in the State of Georgia
• Proven experience as a Principal Investigator or in a similar role

Education Requirements

• Medical degree (MD or DO)

Education Requirements Credential Category

• Medical License

Experience Requirements

• Relevant experience in overseeing clinical trials

Why work in Columbus, GA

Columbus, GA, is known for its vibrant community and quality of life. The city offers various outdoor activities, historical sites, and cultural events, making it an appealing location for both personal and professional growth.