Clinical Research Investigator - Clinical Research (MD or DO) - Monroe, LA Part Time or Full Time
About The Position
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. 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. The IMA group is comprised of three divisions. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities. Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets.
Requirements
- MD or DO degree
- Active medical license
- Prior experience as a Principal Investigator in pharmaceutical clinical trials
- Board certification in internal medicine
Nice To Haves
- Preferably possess diversity and bilingual capabilities
Responsibilities
- 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.
Benefits
- 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
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Ph.D. or professional degree
Number of Employees
501-1,000 employees
