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Skills
- Adverse Eventsunmatched
- Behavioral Healthunmatched
- Certified Clinical Research Coordinator (CCRC)unmatched
- Clinical Researchunmatched
- Clinical Trialunmatched
- Communication Skillsunmatched
- Contract Research Organization (CRO)unmatched
- Dental Insuranceunmatched
- Disability Insuranceunmatched
- Documentationunmatched
- FDA (Food and Drug Administration)unmatched
- Federal Governmentunmatched
- GCP (Good Clinical Practices)unmatched
- Governmentunmatched
- ICH Regulationsunmatched
- IP (Internet Protocol)unmatched
- Institute of Management Accountants (IMA)unmatched
- Investigational New Drug (IND)unmatched
- Maintain Complianceunmatched
- Medicineunmatched
- Needs Assessmentunmatched
- Organizational Skillsunmatched
- Phase II Clinical Trialsunmatched
- Phase IV Clinical Trialsunmatched
- Phlebotomyunmatched
- Problem Solving Skillsunmatched
- Psychologyunmatched
- Regulatory Complianceunmatched
- Safety Standardsunmatched
- Standard Operating Procedures (SOP)unmatched
- Startupunmatched
- Team Playerunmatched
- Vision Planunmatched
- Worker's Compensationunmatched
Description
Description
Clinical Research Coordinator (CRC) – Monroe, LA Advance Your Career While Advancing Medicine
Are you an experienced Clinical Research Coordinator looking to make a meaningful impact? Join IMA Clinical Research in Monroe, LA, where you'll help bring innovative treatments to patients through cutting-edge clinical trials.
As a Clinical Research Coordinator, you'll lead the day-to-day management of industry-sponsored clinical research studies, working alongside physicians, sponsors, and research professionals to ensure every study is conducted with the highest standards of quality, safety, and regulatory compliance. If you're organized, patient-focused, and thrive in a fast-paced environment, we'd love to hear from you.
What You'll Do
- Coordinate all phases of clinical trials from study start-up through closeout.
- Perform phlebotomy and collect study-related samples and data.
- Ensure compliance with FDA, ICH-GCP, sponsor protocols, and site SOPs.
- Educate and support study participants throughout their research journey.
- Collaborate with investigators, sponsors, CROs, IRBs, and laboratory partners.
- Maintain accurate source documentation and report adverse events as required.
What You'll Bring
- 2+ years of Clinical Research Coordinator experience
- Phlebotomy experience required
- Experience with industry-sponsored investigational product (IP) studies required
- Bachelor's degree required; CCRC certification preferred
- Excellent organizational, communication, and problem-solving skills
Why Join IMA Clinical Research?
- Competitive compensation
- Medical, Dental & Vision Insurance
- 401(k) with Company Match
- Generous PTO, Paid Holidays & Floating Holiday
- Tuition Reimbursement & Student Loan Repayment Assistance
- Paid Parental Leave
- Company-paid Life, Short-Term & Long-Term Disability Insurance
Join a collaborative team that's committed to improving lives through clinical research. If you're ready to grow your career while helping shape the future of medicine, we encourage you to apply today.
The IMA Group is an Affirmative Action/Equal Opportunity Employer
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. 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.
#LI-BC1 #LI-ONSITE
Numbers & Facts
| Location | Monroe, Louisiana |
| Industry | Healthcare Services |
| Company Size | 500 to 999 employees |
| Year Founded | 1990 |
| Website | http://www.ima-us.com |
About Company
About The IMA Group
Headquartered in Tarrytown, New York, with its main operations center in Albany, New York, The IMA Group is a national leader with a reputation for providing high-quality medical, psychological and speech and language evaluations. IMA's primary areas of focus are Social Security Disability Consultative Examinations, VA Compensation and Pension Exams, Employability Evaluations, and Occupational Health Services. Our clients include local, state, and federal agencies, as well as private insurers and corporations.
Dr. David Pulver, IMA's President and CEO, is a Board Certified Internist with over thirty years of experience performing disability exams for Social Security Disability. Dr. Pulver has overseen IMA's growth from a single office in White Plains, NY in 1990, to its present status, with over 45 offices throughout New York, Pennsylvania, District of Columbia, Florida, Ohio, New Jersey, Connecticut, Missouri, Virginia and Vermont. Over the past 25 years, IMA has conducted more than 2.5 million evaluations and has grown to a network of more than 500 licensed providers.
IMA Research is a multi-site research company specializing in Phase II, III and IV studies in all primary care disciplines, co-located within many of our facilities. View IMA Research Site
IMA provides a full range of services, including:
Social Security Disability Consultative Examinations VA Compensation and Pension (C & P) Exams Employability Evaluations Substance Abuse Assessments and Monitoring (SAAM) Case Review Occupational Health Evaluations Police Officer/Firefighter Pre-employment Evaluations and Testing Independent Medical Examinations (IME's) (View Our IME Referral Form) Fitness for Duty Exams (FFD) DOT Physicals including Drug and BAT Testing Vocational Rehabilitation Evaluations