Senior Clinical Research Coordintor

Required Education: Bachelors Degree in a Health Profession Physical Science Biological Science or Registered Nurse OR Masters Degree in Physician Assistant AND:

• 48 months of clinical practice nursing or research program coordination experience.

Equivalency-Substitution: Will accept 48 months clinical practice or research program coordinator experience in lieu of the Bachelors Degree for a total of 96 months experience.

Skills:

• Working knowledge of clinical trials protocols.
• Proficient with Microsoft Office to include Outlook Excel Outlook or PowerPoint.
• Ability to communicate verbally or in writing.
• Detail oriented.
• Ability to lead and train other employees.

Certifications:

• Registered Nurse Licensure through the Oklahoma Board of Nursing.
• Physician Assistant Licensure through the Oklahoma Medical Board.

Working Conditions:

• Physical:
  • Sitting for prolonged periods.
  • Manual dexterity.

  • Reaching speaking and listening.

• Environmental:
  • Standard Office Environment.

Why You Belong at the University of Oklahoma:The University of Oklahoma values our communitys unique talents perspectives and experiences. At OU we aspire to harness our innovation creativity and collaboration for the advancement of people everywhere. You Belong Here!

Equal Employment Opportunity Statement:The University in compliance with all applicable federal and state laws and regulations does not discriminate on the basis of race color national origin sex sexual orientation marital status genetic information gender identity/expression (consistent with applicable law) age (40 or older) religion disability political beliefs or status as a veteran in any of its policies practices or procedures. This includes but is not limited to admissions employment housing financial aid and educational services.

Coordinates a clinical research program by identifying and assessing patients distributing information acting as a clinical resource managing data conducting follow-up care for patients attending meetings pertaining to the program and supervising program personnel.

Duties:

• Identifies patients who may be eligible to participate in the research program.
• Performs the initial assessment of potential patients.
• Obtains clinical history and completes patient data forms.
• Provides potential patients with study information.
• Obtains informed consent forms.
• Acts as the immediate clinical resource and the liaison between physicians nurses laboratory personnel etc.
• Performs data management and data analysis.
• Responsible for the initiation organization and carrying out of patient follow-up.
• Assesses patients at all follow-up visits.
• Attends various meetings pertaining to the research program
• May present information.
• May assume the lead role when the supervisor is not available to ensure adherence to protocol.
• May lead and train research personnel.
• Performs various duties as needed to successfully fulfill the function of the position.