Job Description

Job Description

Job Description

Salary:

LOCAL CANDIDATES ONLY

Hours: 10-20 hours per week

Job Summary: We are seeking a dedicated and organized Clinical Research Coordinator (CRC) to support our clinical research division. The CRC will assist with the planning, implementation, and coordination of clinical trials. This position is ideal for individuals with a background in clinical research, nursing, or a related healthcare field, and who are looking for flexible, part-time hours.

Responsibilities:

• Coordinate and manage clinical trial activities, ensuring compliance with protocol, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
• Screen, recruit, and enroll eligible participants for trials, including obtaining informed consent and explaining study requirements.
• Schedule and oversee participant visits and procedures, collect and document data, and manage follow-up as required by study protocols.
• Monitor and report adverse events and study progress to investigators, sponsors, and Institutional Review Boards (IRBs).
• Maintain accurate, organized, and confidential study records, including source documentation, CRFs, and databases.
• Collaborate with study sponsors, monitors, and other team members to support efficient trial conduct and data integrity.
• Assist with study start-up activities, including regulatory submissions, document preparation, and coordination with study sites and vendors.

Qualifications:

• Bachelor’s degree in a healthcare or science-related field (or equivalent experience).
• At least 1 year of experience in clinical research or related field.
• Knowledge of GCP, FDA regulations, and IRB submission processes.
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal abilities to interact with study participants and team members.
• Proficiency in Microsoft Office Suite; experience with electronic data capture (EDC) systems is a plus.

Preferred Qualifications:

• Certification as a Clinical Research Coordinator (e.g., CCRC) or related credential.
• Experience in neurology or similar therapeutic areas is advantageous.

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