Benefits:

Health insurance

Opportunity for advancement

Paid time off

Benefits/Perks

Competitive Compensation

Great Work Environment

Career Advancement Opportunities

Job Summary

We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. The successful candidate will be responsible for overseeing and coordinating clinical research projects, ensuring compliance with regulatory requirements, and maintaining high standards of data integrity and patient care. This is a fully onsite position, requiring the candidate to be present at our Lillington Avenue Office.

Responsibilities

Coordinate and manage clinical trials and research studies from initiation to completion.

Recruit, screen, and enroll study participants.

Obtain informed consent and ensure participants' understanding of study procedures.

Monitor and document participants' progress and adverse events.

Maintain accurate and up-to-date study records and documentation.

Ensure compliance with all regulatory and ethical guidelines.

Assist with data collection, entry, and analysis.

Communicate effectively with research team members, sponsors, and regulatory bodies.

Prepare and submit study-related reports and documentation.

Qualifications

Bachelor's degree in a related field (e.g., life sciences, nursing, public health), (equivalent experience may be accepted)

or, LPN (licensed practical nursing) in lieu of Bachelor's degree

Previous experience in clinical research or a related field is preferred.

Strong organizational and time-management skills.

Excellent communication and interpersonal skills.

Attention to detail and ability to work independently.

Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.

Proficiency in Microsoft Office and research-related software.

Phlebotomy (preferred)

Benefits

Opportunities for professional development and growth.

Collaborative and supportive work environment.

Contribution to meaningful and impactful research.