Research Assistant (Research Nurse/Paramedic/EMT/Phlebotomist/Medical Assistant)

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.

With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Research Assistant (Research Nurse/Paramedic/EMT/Phlebotomist/Medical Assistant)

This role is integral in the execution of all aspects of the clinical trial, will have direct study volunteer contact and is responsible for ensuring that all clinical trial activities are performed as outlined by the clinical trial protocol. You will be responsible for performing all task(s) as per clinical trial protocol, ICON Early Phase Services SOPs, FDA, ICH GCP, and utilizing proper source documentation techniques.  You will participate in clinical trial meetings and training as required based on your role and the requirements of the study.

Responsibilities

• Responsible for performing and documenting clinical trial activities such as (but not limited to):

  • Collection of blood samples

  • Collection of urine or stool samples 

  • Perform ECG

  • Perform Vital Signs

  • Monitor study volunteer activities

  • Other trial related procedures and activities as may be required  

• Conduct study volunteer interviews

• Seek Informed Consent from study volunteers

• Participate in administration of study medications

• Record and follow physician orders as necessary

• Monitor study volunteer for adverse effects and report to study doctors

• Collect and transport clinical safety laboratory specimens

• Provide study volunteer education as required

• Ensure proper use of medical equipment and supplies

• Follow proper disposal processes for all bio-hazardous waste

• Familiarize and understand study protocol requirements –responsible for clarifying any discrepancies or issue to ensure proper study conduct

• Complete peer review quality checks on collected study data

• Apply all IEP CRU Standard Operating Procedures (SOP) applicable to job duties

• Participate in all internal and external clinical trial meetings as appropriate

• Participate trainings as required

• Receive report from outgoing shift and provide report to incoming shift

• Ensure compliance with all applicable regulations (e.g. OSHA, FDA, etc.)

• Undertake other reasonably related duties as may be assigned from time to time.

Education and Experience Requirements

• Minimum of 1 year experience in clinical research or related field preferred

• High School Diploma or equivalency with appropriate licensure or certification as applicable

• Maintains job related competencies, certifications, and/or licensure.  As applicable (CPR, IV, etc.)

• Strong customer service and communication skills

• High level of professionalism

• Interpersonal skills, organizational skills, and teamwork skills.

• Coordinate work to achieve maximum productivity and efficiency

• Ability to work independently and in a team setting

• Effective problem solving skills

• Follows chain of command and directs problems to the appropriate person

• Complies with dress code, maintains a neat and professional appearance

• Knowledge of emergency procedures including fire and evacuation plan

• Experience with phlebotomy across the lifespan.

• Flexible and available based on staffing requirements: weekends, holidays, and on call.

• Capable of handling multiple priorities in a high volume setting.

• Maintains current CPR certifications or ACLS as applicable

• Knowledge of ICH GCP and FDA regulations is a plus

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs.  In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.