Clinical Research Coordinator

Registered Nurse - Clinic

It's more than a career, it's a calling

MO-SSM Health Saint Louis University Hospital 1201 Grand

Worker Type: Regular

Job Highlights:

• Registered Nurse - Clinic!
• Monday - Friday 8-4:30pm!
• No Nights, No weekends, No on-call!

Job Summary:

Carries out assigned phases of investigational clinical studies according to guidelines set forth by the FDA, the IRB (institutional review board), principal investigator(s), and specific stakeholders.

Job Responsibilities and Requirements:

PRIMARY RESPONSIBILITIES

• Coordinates clinical studies in the medical research area.
• Develops an understanding of the requirements of the study protocol and obtains necessary information from physicians and study participants and records this information appropriately. Adheres to protocol in all situations.
• Responsible for recruitment, screening, interviewing and evaluating of study participants.
• Develops advertisement copy and recruitment plan for recruiting study participants. Responsible for development, completion, accuracy and maintenance of patient forms, including the Informed Consent.
• Completes or oversees completion of data entry in a timely manner. Ensures that drug dispensing is performed according to protocol, documented on inventory forms/electronic records, and maintained and updated regularly.
• Responsible for reconciling drug supplies with drug records, for assuring that the study site has adequate drug, biological and other supplies, and for distribution of such to designated individuals.
• Reports all adverse events via appropriate documentation and follows up on incidents.
• Reviews and maintains updated regulatory binder. Responds to quality assurance audit reports in time period required.
• Monitors patient safety, compliance and health status.
• Anticipates study problems, formulates solutions and determines resolutions.
• Responsible for all aspects of study termination, i.e. completes necessary documents/forms, return of drugs to drug company, etc.
• Develops and maintains communication with the research manager, co-workers, principal investigators, and other internal personnel regarding study related issues.
• Prepares for and meets with pharmaceutical monitors site visits. Maintains professional relationships with external customers.
• Participates in department staff meetings, study planning and special projects as appropriate.
• Attends and participates in investigator meetings as required by pharmaceutical companies.
• Communicates necessary information with sponsors, monitors, patients, physicians, co-workers, and others in a courteous and professional manner.
• Exhibits an ability to work in a collaborative, effective manner with all necessary research team members in order to meet the research objectives. Serves as a liaison between physicians, drug companies, research organizations, staff and patients.
• Develops and maintains professional communication with monitors, sponsors, and potential sponsors in such areas as initiation visits, monitor visits, investigator meetings.
• Works in a constant state of alertness and safe manner.
• Performs other duties as assigned.

EDUCATION

• Graduate of accredited school of nursing

EXPERIENCE

• One year registered nurse experience

PHYSICAL REQUIREMENTS

• Frequent lifting/carrying and pushing/pulling objects weighing 0-25 lbs.
• Frequent sitting, standing, walking, reaching and repetitive foot/leg and hand/arm movements.
• Frequent use of vision and depth perception for distances near (20 inches or less) and far (20 feet or more) and to identify and distinguish colors.
• Frequent use of hearing and speech to share information through oral communication. Ability to hear alarms, malfunctioning machinery, etc.
• Frequent keyboard use/data entry.
• Occasional bending, stooping, kneeling, squatting, twisting and gripping.
• Occasional lifting/carrying and pushing/pulling objects weighing 25-50 lbs.
• Rare climbing.

REQUIRED PROFESSIONAL LICENSE AND/OR CERTIFICATIONS

Resuscitation Certification Requirement: Basic Life Support Healthcare Provider (BLS HCP) required within 90 day of employment. Other resuscitation certifications may be required dependent on department.

State of Work Location: Illinois Basic Life Support HealthCare Provider (BLS HCP) - American Heart Association (AHA) And Registered Professional Nurse (RN) - Illinois Department of Financial and Professional Regulation (IDFPR)

• Basic Life Support HealthCare Provider (BLS HCP) - American Heart Association (AHA)
• And
• Registered Nurse (RN) - Missouri Division of Professional Registration
• Or
• Registered Nurse (RN) Issued by Compact State

State of Work Location: Oklahoma

• Basic Life Support HealthCare Provider (BLS HCP) - American Heart Association (AHA)
• And
• Registered Nurse (RN) Issued by Compact State
• Or
• Registered Nurse (RN) - Oklahoma Board of Nursing (OBN)

State of Work Location: Wisconsin

• Basic Life Support HealthCare Provider (BLS HCP) - American Heart Association (AHA)
• And
• Registered Nurse (RN) Issued by Compact State
• Or
• Registered Nurse (RN) - Wisconsin Department of Safety and Professional Services

Work Shift:

Day Shift (United States of America)

Job Type:

Employee

Department:

4954000235 Internal Medicine Gen - Admin Scheduled Weekly Hours: 40

Benefits:

• Paid Parental Leave: we offer eligible team members one week of paid parental leave for newborns or newly adopted children (pro-rated based on FTE).
• Flexible Payment Options: our voluntary benefit offered through DailyPay offers eligible hourly team members instant access to their earned, unpaid base pay(fees may apply)before payday.
• Upfront Tuition Coverage: we provide upfront tuition coverage through FlexPath Funded for eligible team members.

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SSM Health is an equal opportunity employer. SSM Health does not discriminate on the basis of race, color, religion, national origin, age, disability, sex, sexual orientation, gender identity, pregnancy, veteran status, or any other characteristic protected by applicable law.