- Search jobs
- New Orleans, LA
- clinical data manager
Clinical data manager Jobs in New Orleans, LA
Create a job alert for this search
Clinical data manager • new orleans la
- Promoted
Clinical Research Coordinator Lead / Manager - 248029
MedixNew Orleans, LA, USData Architect- Manager
PwCNew Orleans,LAClinical Manager
ChenMedNew Orleans, LA, United States- Promoted
Senior Clinical Study Manager (Remote)
StrykerNew Orleans, LA, USSenior Manager, Clinical Data Management
VirtualVocationsNew Orleans, Louisiana, United StatesCLINICAL MANAGER
RHDNew Orleans, LA, USManager, Data Operations, Data Engineer
KPMGNew Orleans, LA- Promoted
Clinical Scientist - Clinical Surveillance & Training (Clinical Psychologist / Neuropsychologist)
Syneos Health / inVentiv Health Commercial LLCNew Orleans, LA, United StatesClinical Data Manager, CHERISH
Tulane University StaffNew Orleans, LA, United StatesData Manager
FirstLine SchoolsNew Orleans, LA, USClinical Training Manager
Goodwin RecruitingNew Orleans, LouisianaeCommerce Data Manager
Singer IndustrialBelle Chasse, LA, US- Promoted
Clinical Data Manager, CHERISH
InsideHigherEdNew Orleans, Louisiana, United StatesManager of Clinical Operations
Upward HealthNew Orleans, Louisiana, United States, 70112- Promoted
Senior Clinical Trial Manager- APAC
Dianthus TherapeuticsNew Orleans, LA, USHigh School Data Manager
KIPP New Orleans SchoolsNew Orleans, LA, US- Promoted
Payer STARS / Quality Clinical Consultant, Senior Manager
Louisiana StaffingNew Orleans, LA, USCLINICAL TRIALS MANAGER
LSU Health Sciences CenterNew Orleans- Promoted
Regulatory Manager / Senior Regulatory Manager (Clinical Trials)
Precision MedicineNew Orleans, LA, US- physician (from $ 59,949 to $ 242,814 year)
- owner operator (from $ 60,000 to $ 240,000 year)
- director of software engineering (from $ 185,000 to $ 239,875 year)
- freelance writing (from $ 38,002 to $ 232,781 year)
- crna (from $ 50,000 to $ 228,000 year)
- independent contractor (from $ 48,750 to $ 225,000 year)
- associate dentist (from $ 50,000 to $ 225,000 year)
- chief financial officer (from $ 125,000 to $ 225,000 year)
- general counsel (from $ 125,842 to $ 222,103 year)
- principal software engineer (from $ 144,814 to $ 222,072 year)
- Austin, TX (from $ 58,750 to $ 238,120 year)
- San Diego, CA (from $ 125,000 to $ 175,295 year)
- Chicago, IL (from $ 120,000 to $ 165,750 year)
- New York, NY (from $ 124,700 to $ 162,500 year)
- Los Angeles, CA (from $ 85,000 to $ 160,000 year)
- Orange, CA (from $ 105,000 to $ 159,260 year)
- Phoenix, AZ (from $ 119,875 to $ 154,500 year)
- Atlanta, GA (from $ 110,000 to $ 146,250 year)
- Irvine, CA (from $ 105,000 to $ 139,875 year)
- Dallas, TX (from $ 100,000 to $ 131,640 year)
The average salary range is between $ 105,689 and $ 162,500 year , with the average salary hovering around $ 129,500 year .
Related searches
Clinical Research Coordinator Lead / Manager - 248029
MedixNew Orleans, LA, US- Full-time
Job Title : Lead Clinical Research Coordinator (CRC)
Location : New Orleans, LA
Schedule : Monday–Friday, 9 : 00 AM–5 : 00 PM (On-site)
Type : Contract-to-Hire, 6 month
Pay : $32-$40 / hour
Overview
We are seeking an experienced and driven Lead Clinical Research Coordinator to help build and lead a brand-new research department from the ground up. This individual will serve as both a hands-on coordinator and a leader, managing all aspects of clinical trials while guiding a new physician and eventually mentoring a team of CRCs. This is a unique opportunity for someone eager to take ownership, grow into a management role, and be the backbone of a developing clinical research program.
Key Responsibilities
- Serve as the primary point of contact for all clinical research activities at the site.
- Perform end-to-end study coordination, from startup and recruitment through closeout.
- Prepare and manage study documentation, including regulatory binders, source documents, and eSource / CTMS data entry.
- Conduct participant visits, including consent, assessments, and procedures such as phlebotomy and EKGs as needed.
- Oversee participant recruitment using EMR systems and community outreach initiatives.
- Ensure all studies are conducted in compliance with FDA, ICH-GCP, and sponsor requirements.
- Maintain meticulous documentation and quality control across all studies to ensure audit readiness.
- Collaborate with and train a new physician principal investigator (PI), providing guidance on research processes and best practices.
- Lead and mentor future CRC hires, delegating tasks, conducting quality reviews, and maintaining workflow balance.
- Manage investigational product accountability and study supply inventory.
- Prepare for and participate in sponsor, CRO, and FDA monitoring visits or audits.
- Over time, assume expanded responsibilities such as budget negotiations and contract management.
Typical Day Breakdown
Qualifications (Must-Have)
Preferred Skills (Nice-to-Haves)
Why This Role Is Exciting
This role is ideal for an experienced CRC who thrives in dynamic settings, loves taking initiative, and wants to grow into leadership.