We are seeking a competent, proactive, self-directed, experienced clinical research coordinator with effective time management skills to assist our clinical research organization. The Clinical Research Coordinator works under the direction of the research director and the Principal Investigator (PI). The CRC supports the daily clinical trial activities and plays a critical role in the conduct of the study.

Responsibilities

• Overseeing the running of clinical trials

• Collecting data obtained from study participants.

• Communicating with participants regarding study objectives

• Administering questionnaires and monitoring participants to ensure they adhere to the study’s protocol.

• Liaising with laboratories regarding research findings.

• Monitoring the study to ensure that it complies with protocols, is ethically conducted, and follows regulatory standards

• Maintaining research records of study activity, including case report forms, drug dispensation records, or other regulatory forms as per FDA guidelines

• Directing the collection, labeling, storage, and transport of all specimens

• Making sure that all equipment and supplies needed for the study are in stock and in good working order

Qualifications

· Bachelor's degree, preferred medical/health science.

· Clinical Research experience.

· Bilingual English / Arabic is preferred