Coordinator-Clin Research 2

Loma Linda University Health • Loma Linda, CA

4d

About The Position

The Coordinator-Clinical Research 2 assists with and coordinates activities associated with clinical research conducted by LLUHC. Coordinates care, screening, recruitment, research exams, medical record review, and data entry; prepares study related documents as outlined by the research protocol. Collects and processes required specimens within scope of training. May perform physical measurements, vital signs and other diagnostic tests as stipulated by study protocols and within scope of training. Maintains accurate documentation and study records and may obtain informed consent for non-interventional studies. Maintains current knowledge of all industry trends affecting national and local research activity. Works independently and balances priorities upon receipt of project direction of supervisor and Principal Investigator (PI). Performs other duties as needed.

Requirements

• High School Diploma or GED required.
• Minimum one year clinical research experience required.
• Minimum two years health care and computer experience required.
• Knowledge of HIPAA guidelines; handling Biohazard materials; good clinical practice; ICH guidelines.
• Read, write legibly; speak in English (and Spanish preferred) with professional quality; use computer and software programs necessary to the position; troubleshoot and calibrate patient care equipment.
• Relate and communicate positively, effectively, and professionally with others; be assertive and consistent in following and/or enforcing policies; work calmly and respond courteously when under pressure; lead, supervise, teach, and collaborate; accept direction.
• Communicate effectively in English in person, in writing, and on the telephone; think critically; work independently with minimal supervision; perform basic math functions; manage multiple assignments effectively; work well under pressure; problem solve; organize and prioritize workload; recall information with accuracy; pay close attention to detail.
• Distinguish colors and smells as necessary for patient care; hear sufficiently for general conversation in person and on the telephone; identify and distinguish various sounds associated with the work place/patient care; see adequately to read computer screens, medical records, and written documents necessary to position; discern temperature variances through touch.
• Basic life Support (BLS) certification from the American Heart Association (AHA) required.
• Certified Clinical Research Coordinator (SoCRA, ACRP) required within one year of eligibility.
• International Air Transportation Association (IATA) Certificate required within 90 days of hire.

Nice To Haves

• Bachelor's Degree preferred.
• Certified Medical Assistant (MA) or Certified Nursing Assistant (CAN) preferred.
• Phlebotomy Certified preferred.

Responsibilities

• Coordinates care, screening, recruitment, research exams, medical record review, and data entry
• Prepares study related documents as outlined by the research protocol
• Collects and processes required specimens within scope of training
• May perform physical measurements, vital signs and other diagnostic tests as stipulated by study protocols and within scope of training
• Maintains accurate documentation and study records
• May obtain informed consent for non-interventional studies
• Maintains current knowledge of all industry trends affecting national and local research activity
• Works independently and balances priorities upon receipt of project direction of supervisor and Principal Investigator (PI)
• Performs other duties as needed.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 5,001-10,000 employees