Senior Clinical Research Coordinator

Society for Conservation Biology; Los Angeles (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading organization in medical innovation is seeking a Senior Clinical Research Coordinator to lead their clinical operations team in Los Angeles. The role involves managing clinical trials, training staff, and ensuring compliance with protocols. Ideal candidates will have a strong background in clinical research, particularly in neurology, and excellent organizational skills.

Qualifications

• At least 2 years of experience in clinical research required.
• Prior experience supporting neurology studies preferred.

Responsibilities

• Manage, train, and support clinical site staff.
• Conduct and manage clinical trials according to study protocol.
• Ensure compliance and productivity of all clinical site operations.

Skills

Leadership

Communication

Attention to Detail

Organization

Multi-tasking

Education

Associate's Degree

Healthcare Certification

Job description

Job Description

JOB LOCATION/SCHEDULE: Monday - Friday / On-Site / Los Angeles

COMPANY OVERVIEW: At Alliance Clinical Network, we're a team dedicated to advancing medical innovation and healing technology through groundbreaking research. We are passionate about improving patient lives every day.

SUMMARY: We are seeking a Sr Clinical Research Coordinator to join ACN and lead our clinical operations team at our Los Angeles location. This role offers the opportunity to train and support staff managing multiple studies. If you're an enthusiastic, detail-oriented lead CRC looking for your next step, we'd like to meet you.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

1. Partner with the Regional Site Director to ensure compliance and productivity of all clinical site staff and operations.
2. Manage, train, and support clinical site staff.
3. Review, understand, and communicate study protocols.
4. Oversee Site Initiation Visit (SIV), Pre-Study Validation Visit (PSV), and Interim Monitoring Visit (IMV).
5. Assist CRC team as needed to facilitate research and business needs.
6. Conduct and manage clinical trials according to study protocol guidelines and internal SOPs.
7. Ensure all data is entered into the sponsor's data portal and all queries are resolved promptly.
8. Work closely with CRO/CRA and IRB.
9. Perform administrative tasks such as ordering supplies and equipment for the study.
10. Manage all required study start-up documentation, training, and timelines for assigned protocols.

QUALIFICATION REQUIREMENTS:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made for individuals with disabilities.

EDUCATION AND EXPERIENCE:

• Prior experience in clinical research, preferably supporting neurology studies, is strongly preferred.
• Associate's degree and/or completion of an accredited healthcare certification program is required.
• Comfortable stepping into a leadership role.
• At least 2 years of experience in clinical research is required.
• At least 2 years' experience working as a Clinical Research Coordinator is preferred.
• Comprehensive knowledge of FDA, GCP, and confidentiality standards.
• Exceptional attention to detail and organization skills.
• Excellent written and verbal communication skills.
• Proven ability to multi-task in a rapidly changing environment.

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