What are the responsibilities and job description for the Clinical Research Investigator - Clinical Research (MD or DO) - Monroe, LA *Part Time or Full Time position at The IMA Group?
Description
Company Overview:
The Clinical Research Division at The IMA Group is a dynamic hub of expertise and innovation, dedicated to advancing healthcare through clinical trials and studies. Our team of seasoned professionals collaborates with industry leaders, conducting patient-centric research across diverse therapeutic areas. Committed to ethical practices and regulatory compliance, we aim to pioneer groundbreaking medical solutions that shape the future of healthcare.
Job Summary:
Are you a board-certified MD or DO with a background in psychiatry or neurology, and a passion for advancing medical science? IMA Clinical Research is seeking a dedicated and detail-oriented Clinical Research Investigator to join our dynamic team at our Monroe, LA location.
You'll serve as a Principal Investigator (PI) on pharmaceutical industry-sponsored clinical trials, playing a key part in groundbreaking research that impacts lives.
What We Offer:
Company Overview:
The Clinical Research Division at The IMA Group is a dynamic hub of expertise and innovation, dedicated to advancing healthcare through clinical trials and studies. Our team of seasoned professionals collaborates with industry leaders, conducting patient-centric research across diverse therapeutic areas. Committed to ethical practices and regulatory compliance, we aim to pioneer groundbreaking medical solutions that shape the future of healthcare.
Job Summary:
Are you a board-certified MD or DO with a background in psychiatry or neurology, and a passion for advancing medical science? IMA Clinical Research is seeking a dedicated and detail-oriented Clinical Research Investigator to join our dynamic team at our Monroe, LA location.
You'll serve as a Principal Investigator (PI) on pharmaceutical industry-sponsored clinical trials, playing a key part in groundbreaking research that impacts lives.
What We Offer:
- Flexible scheduling – ideal for professionals seeking part-time, full-time, or 1099 contract opportunities
- A collaborative and supportive research environment
- The chance to contribute to cutting-edge studies in mental health, neurology, and beyond
- Oversee staff and delegate duties accordingly.
- Provide required documentation to Sponsor and IRB.
- Maintain licenses for PI/Sub-I roles.
- Conduct and supervise on-site investigations to ensure thorough and accurate assessments.
- Screen potential subjects based on study criteria.
- Ensure thorough documentation compliance.
- Assess and report safety data and protocol issues.
- MD or DO degree
- Active medical license
- Prior experience as a Principal Investigator in pharmaceutical clinical trials
- Preferably possess diversity and bilingual capabilities
- Board certification in internal medicine
- Competitive salary
- Health, Dental, Vision Insurance
- Opportunities for professional development and growth
- A supportive and inclusive work environment
- Paid time off, holidays and a floating holiday
- 401k with employer match
- LTD, STD, Flexible Spending Account, Company paid life insurance and ADD
- Equality Opportunity Employer
- Tuition Reimbursement Program
- Maternity leave