Ochsner Clinic Foundation
Senior Clinical Research Coordinator-Biorepository and Core Research Laboratory
New Orleans - New Orleans Region - Louisiana · Senior
Sponsorship not specified$20k-$50kDetected 1 day ago
AccessibilityEpicClinical TrialsClinical ResearchPharmacy PracticePatient CareClinical Laboratory TechniquesResearchLeadershipCommunicationTime ManagementMentoringGxP
About the role
- We believe that every award earned, every record broken and every patient helped is because of the dedicated employees who fill our hallways.
- This job description is a summary of the primary duties and responsibilities of the job and position.
- It is not intended to be a comprehensive or all-inclusive listing of duties and responsibilities.
Responsibilities
- Ability to develop study related budgets, contracts, and patient consent documents.
- Strong organizational and time management skills and ability to multi-task, pay close attention to detail, and develop new techniques.
- Current Basic Life Support (BLS) certification from the American Heart Association within 60 days of hire.
- Maintains close communication with study sponsor representatives including but not limited to site initiation, maintenance, and close out of studies.
- Completes data entry into sponsor-specific data entry systems and/or supports data coordinator, including query resolution and transcribes information across various internal and external electronic data systems.
- Performs other related duties as assigned.
Requirements
- Required - High school diploma or equivalent.
- 5 years of relevant research experience in a clinical setting,
- Familiarity with and understanding of lean management principles.
- Ability to follow and provide critical feedback on the investigational plan.
- Ability to mentor junior staff members on the requirements and regulations associated with the conduct of clinical trials and other related research activity.
- Expertise in using computers and web-based applications including working knowledge of Epic (Super-Users).
- Effective verbal and written communication skills and ability to present information clearly and professionally to varying levels of individuals throughout the patient care process.
- Strong interpersonal and leadership skills and ability to coach others, as well as effectively work independently.
- Performs clinical laboratory activities as required per protocol and maintains study supplies and equipment.
- Develops and maintains all required documentation as it relates to the conduct of assigned clinical trials and associated patient care.
Skills
- Knowledge Skills and Abilities (KSAs)
Compensation
- $20k-$50k
Benefits
- Knowledge of medical and clinical research terminology and processes.
- Ability to travel throughout and between facilities and work a flexible work schedule, including on-call, weekend, and night shifts.
Company info
- Are you ready to make a difference?
Visa & Work Authorization
- Maintains close communication with study sponsor representatives including but not limited to site initiation, maintenance, and close out of studies
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