Must have experience in clinical research in diabetes, hypertension and high cholesterol studies. Strong recruitment and retention for clinical trials.•

Bilingual:

English/Spanish is a must.

DUTIES:

Provide coordination of study-related activities for patients enrolled in research studies Ensure that clinical research activities are performed in accordance with local and federal regulations and adhere to policies and procedures of the sponsors and CROs. Assist in IRB submissions and maintain regulatory documents. Confer with members of the clinical team to confirm appropriateness of enrolled subjects. Able to take vitals signs, EKG and draw blood samples. Enter research data into a centralized database as per protocol requirements and answer queries in a timely manner. . Prepare study materials such as informed consent documents, source documents, case report forms, enrollment logs and drug accountability logs. Position is an excellent opportunity for recent graduates who are interested to pursue a career in the medical field.

Job Type:

Full-time.

Job Types:

Contract, Full-time Pay:

$38,000.00 - $45,000.00 per year

Benefits:

401(k) Dental insurance Health insurance Paid time off Vision insurance

Education:

Bachelor's (Preferred)

Work Location:

In person