Clinical Research Coordinator Jobs

Clinical Research Coordinator

Under general supervision of Principal Investigator and Research Manager, Coordinator will perform more specialized clinical duties to assist in the conduction of a research project. Research Coordinator should require minimal supervision and demonstrate proficiency in research techniques. Should have the ability to teach and train other personnel as needed. At the discretion and under the supervision of the Manager, Coordinator may perform more complex tasks and assume greater responsibilities as needed for a project.

Principal Duties and Responsibilities

·Screen patients for eligibility on clinical trials per protocol and ICH guidelines.

·Coordinate patient entry, on-study and follow-up on a variety of clinical trials. This includes assuring patient eligibility.

·Perform protocol required clinical procedures such as blood draws, and support medical provider on other clinical procedures (e.g., physical exams, injections)

·Verify study samples are collected and processed through approved protocols.

·Complete case report forms and source documents.

·Maintain communication with the study sponsors, IRB’s, and central and local laboratories.

·Maintain constant communication with Principal Investigator and Research Manager regarding patient care issues.

·Conduct and Coordinate study monitoring visits.

·Maintain protocol notebooks and consent form files. Routinely monitor inventory of all research supplies and order as needed.

·Maintain Institutional Review Board protocol standards.

·Dispense, maintain, and record Investigational Product per protocol and ICH guidelines.

·Assist with training and supervision of Research Assistant.

Preferred Skills:

• Excellent research management skills.
• Phlebotomy experience a PLUS.
• Excellent interpersonal skills, openness to feedback, and a desire to learn and improve skills.
• Ability to work autonomously, remotely, in dynamic fast-paced environments, using problem solving skills to adapt to changing demands.
• Basic understanding of statistical data analysis and interpretation.
• CCRC certification a PLUS.
• Great attention to detail.
• Excellent communication skills, and a history of project management. Ability to convey and/or receive written/verbal information to/from various audiences in different formats.

Qualification:

• 1-3 years of clinical research experience preferred
• BS, MS, MD, nursing degree or relevant clinical research experience in a related discipline