Clinical Research Coordinator

Northshore Research Associates; Alexandria (LA); Sur place; USD 50 000 - 70 000; Plein temps

Résumé du poste

Northshore Research Associates is seeking a Clinical Research Coordinator for an on-site CRC role in Alexandria, LA. You will coordinate participant screening, enrollment, and follow-up, ensuring protocol compliance and data quality across studies.

Educators with healthcare or life science backgrounds are preferred; strong communication, data handling, and regulatory documentation skills are essential to protect participant safety and integrity of trial data.

Qualifications

• Clinical research experience including involvement in clinical trials and knowledge of GCP.

Responsabilités

• Coordinate and manage participant screening, enrollment, and follow-up per study protocols.

Connaissances

Clinical research experience

Informed consent processes

Protocol adherence monitoring

Data management

Regulatory knowledge (GCP, HIPAA)

Communication and interpersonal skills

Organizational/time-management

Formation

Associate or Bachelor’s degree in nursing, biology, public health, or related field

Clinical Research Coordinator certification (a plus)

Description du poste

Company Description

Northshore Research Associates is dedicated to conducting high-performing, patient-centered clinical trials with a focus on speed, quality, and integrity. The organisation aims to expand access to innovative therapies, particularly in underserved and rural communities, by partnering closely with patients and healthcare providers. Northshore Research Associates emphasizes the generation of reliable clinical data that support the development of safe and effective treatments. Team members contribute to meaningful research that helps bring new therapeutic options to diverse populations while maintaining strong ethical and regulatory standards.

Role Description

The Clinical Research Coordinator is a full-time, on-site role based in Alexandria, LA. This role is responsible for coordinating and managing clinical trial activities, including participant screening, enrollment, and follow-up according to study protocols. Daily tasks include obtaining and documenting informed consent, scheduling and conducting study visits, collecting and entering source data, and maintaining accurate study records. The coordinator will collaborate with investigators, sponsors, and regulatory staff to ensure protocol compliance, support monitoring visits, and assist with regulatory submissions and reporting. The role also involves educating participants about study procedures, safeguarding participant safety, and helping optimise study workflows to meet timelines and quality standards.

Qualifications

• Demonstrated clinical research experience, including involvement in clinical trials and familiarity with Good Clinical Practice (GCP).
• Ability to manage informed consent processes, ensuring clear communication, documentation, and participant understanding.
• Knowledge of study protocol requirements and the ability to implement and monitor protocol adherence in daily research activities.
• Strong research and data management skills, including accurate data entry, source documentation, and maintenance of regulatory binders.
• Relevant healthcare or life sciences education (e.g., associate or bachelor’s degree in nursing, biology, public health, or related field); certification as a Clinical Research Coordinator is a plus.
• Effective communication and interpersonal skills for working with participants, investigators, and multidisciplinary teams.
• Organizational and time‑management skills, with attention to detail and the ability to handle multiple studies or tasks simultaneously.
• Comfort working in a clinical setting and adhering to institutional, ethical, and regulatory requirements, including HIPAA and safety protocols.