RN Research Coordinator

GI Alliance is seeking an experienced RN Research Coordinator.

Duties of this position include, but are not limited to, the following:

Position purpose

The Nurse Research Coordinator is a specialized research professional working with and under the direction of the Director and Clinical Principal Investigator (PI). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Responsibilities/Duties/Functions/Tasks:

• Communicate study requirements to all individuals involved in the study.

• Develop and implement recruitment strategies in accordance with GI Alliance RESEARCH and IRB requirements and approvals.

• Screen subjects for eligibility using protocol specific inclusion and exclusion criteria.

• Entry of participant information and study visit procedures into the Clinical Trial Management System to ensure billing to appropriate funding source.

• Maintains adequate inventory of study supplies. When handling investigational drugs/devices, follows the sponsor protocol and/or GI Alliance RESEARCH Policy on Investigational Drug/Device Accountability.

• Complete study documentation and maintenance of study files in accordance with sponsor requirements and GI Alliance RESEARCH policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.

• Maintains effective and ongoing communication with sponsor, research participants, Director and PI during the course of the study.

• Manage the day to day activities of the study including problem solving, communication and protocol management.

• Collects and reports ongoing patient recruitment/ enrollment metrics to Director and PI.

• Arranges secure storage of study documents that will be maintained according to Good Clinical Practice guidelines or for the contracted length of time, whichever is longer.

• Protects the rights and welfare of all human research participants involved in research in accordance with Federal regulations

• Cooperates with GI Alliance RESEARCH compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance to the appropriate compliance office.

• Other duties as assigned.

Qualifications

Qualifications

Experience:

• RN license required
• 1-3 years of Clinical Research Coordinating experience preferred

Other Requirements: None

Performance Requirements:

• Knowledge of grammar, spelling, and punctuation.

• Knowledge of purchasing, budgeting, and inventory control.

• Skill in taking and transcribing dictation and operating office equipment.

• Skill in answering the phone and responding to questions.

• Skill in time management, prioritization, and multitasking.

• Skill in writing and communicating effectively.

• Ability to work under pressure, communicate and present information.

• Ability to read, interpret, and apply clinic policies and procedures.

• Ability to identify problems, recommend solutions, organize and analyze information.

• Ability to multi-task, establish priorities, and coordinate work activities.

• Ability to competently use Microsoft Office, including Word, PowerPoint, Excel, and appropriate practice management software.

GI Alliance is an Equal Opportunity Employer. We are committed to creating an inclusive, welcoming, and equitable work environment. Our company values and celebrates the diversity of our physicians, staff and patients. We firmly believe our service is greatly enriched by our diversity of thought, experience, perspective, culture, and background.

Please Note: All job offers are contingent on the successful completion of pre-employment criminal history check.

NOTE: ALL APPLICATIONS MUST BE COMPLETED IN FULL FOR CONSIDERATION.

No phone calls or agencies, please.

EEO/AA-M/F/disabled/protected veteran