Senior Clinical Research Coordinator

Tulane University; New Orleans (LA); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Senior Clinical Research Coordinator to oversee clinical trials related to cardiovascular disease. This pivotal role involves managing research staff, ensuring compliance with protocols, and acting as a liaison among various stakeholders. The ideal candidate will possess strong organizational and communication skills, with a background in clinical research. This position offers the opportunity to make a significant impact in the field of healthcare research while working in a dynamic and supportive environment. If you are passionate about advancing clinical research and improving patient outcomes, this role is for you.

Qualifications

• 5 years of experience in clinical research or 2 years with a Master's Degree.
• Experience in supervising and training clinical staff.

Responsibilities

• Manage clinical trials and epidemiological studies related to cardiovascular disease.
• Supervise research staff and ensure compliance with protocols.

Skills

Supervising research staff

Organizational skills

Analytical skills

Interpersonal skills

Communication skills

Software proficiency (Access, PowerPoint, Excel, Word)

Confidentiality

Event organization

Detail-oriented

Willingness to travel

Education

Bachelor’s Degree or RN licensure

Master’s Degree in related field

Tools

Access

PowerPoint

Excel

Word

Job description

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Job Summary

The primary responsibility of the Senior Clinical Research Coordinator is to manage all aspects of conducting clinical trials and epidemiological studies related to cardiovascular disease. They supervise and direct activities of research staff to ensure compliance with protocols and clinical objectives. The role requires in-depth knowledge of protocol requirements and good clinical practices per federal regulations. The Senior Clinical Research Coordinator acts as a liaison among patients, investigators, collaborators, IRB, and sponsors. They recruit, screen, enroll, and follow study patients, oversee data collection and quality control, and ensure protocol adherence and patient monitoring. They work independently to design, coordinate, and implement research projects, maintain regulatory documentation, report adverse events, and train staff. They may perform procedures such as ECGs, vital signs, and laboratory processing as needed. This role also supervises clinical research staff to ensure compliance with all regulatory and institutional standards.

Required Knowledge, Skills, and Abilities

• Experience supervising and training research staff in a clinical or medical setting.
• Excellent organizational, analytical, interpersonal, and communication skills.
• Proficiency in software such as Access, PowerPoint, Excel, and Word.
• Ability to interact well with patients and the public.
• Ability to work independently and maintain confidentiality.
• Skilled in organizing meetings and events, with willingness to assume additional duties.
• Highly organized and detail-oriented to ensure protocol adherence and participant contact at scheduled times.
• Willingness to travel for clinic visits and meetings.
• Availability for weekend and evening work for emergencies or participant questions.

Educational and Experience Requirements

• Bachelor’s Degree or RN licensure with 5 years of related experience.
• OR Master’s Degree in a related field with 2 years of related experience.

Preferred Qualifications

• Certification as a CCRC or CCRP.
• Master’s Degree in Epidemiology, Clinical Research, or Public Health.
• Experience in writing Study Protocols and SOPs.

Additional Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Research, Analyst, IT
• Industry: Higher Education