events | Clinical Research Nurse (Study Coordinator) I in Germantown, WI

Clinical Research Nurse (Study Coordinator) I

  • Select Source International
  • $45,310.00 - 70,020.00 / Year *
  • W163N11861 W Fond Du Lac Ave
  • Germantown, WI 53022
  • Full-Time
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SELECT SOURCE INTERNATIONALSelect Source International (SSI) has been serving major corporations for more than 15 years. At SSI, we believe in building a corporation with only the strongest and most capable individuals. Our world-class consultants have the expertise to meet our clients demands. Here at SSI, we pride ourselves on the fundamental belief that our team is essential to our companys growth. We assist our consultants every step of the way in order to match them to the best possible position for their skills. Position: Clinical Research Nurse (Study Coordinator) I Location: Neenah, WI Duration: 12 Months Extension Job Summary: A clinical research nurse (also known as a Study Coordinator in the clinical research industry) is a professional who will coordinate and oversee clinical operations of research projects. This person will participate in assessing, planning, implementing and evaluating subject treatment and safety in clinical research studies and will comply with established clinical research organizational policies and procedures, as well as carry out research. This person will work under the general supervision of the Principal Investigator/Clinical Research Manager (PI/CRM) responsible for the clinical studies. Duties and Responsibilities Obtain and review records for potential research subjects; maintain study records of research subjects that include documentation of study procedures and progress of research study subjects, following guidelines set forth by the protocol sponsors. Review recruited clinical study subjects for eligibility; schedule appointments and interviews, and evaluate potential subjects. Instruct potential research subjects and responsible family members, nursing staff, and ancillary staff involved in research on the study procedures, treatments, and side effects. Educate subjects concerning protocol and explain informed consent procedures, including HIPAA authorizations and obtain subjects written consent. Evaluate and assist in developing subject education materials and give subjects and/or family members instruction on test article administration and other study information. Perform nursing assessments and monitor subjects progress during clinical studies and notify PI/CRM of any adverse events and serious adverse events, including evidence of unexpected side effects. Perform initial interview during each subject visit and plan appropriate procedures according to the protocol. Coordinate research activities and procedures for study subjects. Complete case report forms for each study participant and document study data in subject study file. Assess and document compliance of research subjects. Attend staff meetings/conferences as part of a study team. Act as principal investigators representative as appropriate. Maintain subject database information. Work with analysts and assist with queries related to data to evaluate the significance of compiled data. Attend research meetings and conferences as required. Provide orientation, information, training/cross-training, and assistance for new/existing personnel and research assistants, study staff to the research activities. Participate in staff meetings and in-service education. Maintain adequate inventory of research supplies necessary for research activities. Maintain exam rooms and laboratory. Qualifications Licensed Practical Nurse (LPN) or Registered Nurse (RN) One year of licensed or registered professional nursing experience Excellent oral and written communication skills High degree of empathy for subjects Ability to work independently. Strong problem-solving abilities Understands OSHA guidelines for handling hazardous biological and chemical materials Must have Pediatric, OB-Gyn, geriatric, hospital experience. Not looking for Occupation Health experience Varied hours 10-30 per week, sometimes up to 40 While we sincerely appreciate all applicants, only those get selected for interview will be contacted. Note: Selected candidates will be required to submit to a Background Check and a Drug Screen. Thanks and Regards Kranthi Kumar Sr. Technical Recruiter 6311 Wayzata Blvd;Suite 150, Minneapolis, Minnesota 55416 (Work: 952-###-#### Ext: 5010, *Email: ...@selectsourceintl.com Disclaimer: Select Source International (SSI) does not tolerate discrimination against any applicant on the basis of gender, sexual orientation, race, religion, national origin, ethnicity, veteran status, disability, age, sexual preference or any other protected status designated by federal, state or local law. It is SSIs policy to affirmatively recruit, hire, train, assign, transfer, evaluate, compensate, provide benefits, promote, demote, layoff, recall, and terminate employees on their own abilities, achievements and experiences. This policy applies to all SSI employee activities. SSI encourages diversity in hiring, recognizing that this enriches the work environment for all SSI associates and that a broad variety of perspectives enhances decision-making and creativity.

SSI is an Equal Opportunity Employer. If you require accessibility assistance applying for any of our positions, please send an email with your request to ...@selectsourceintl.com
Associated topics: assessments, certified nursing, clinical, cns, fnp, locum, neighborcare, nurse practitioner, prn, spanish


* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.