Listing details
- Posted Feb 24
- Last verified Oct 31
About the job
- Following detailed instruction, will screen, recruit and enroll participants for assigned studies by interviewing potential participants and reviewing medical history to determine if eligibility requirements are met.
- Under direction, will inform and instruct study participants concerning research protocol and complete the patient informed consent procedure.
- Under direction of PI, assist with coordinating and and/or performing research testing per protocol such as drawing blood, vital signs, EKGs, etc., includes processing and packaging of laboratory samples for shipment.
- With detailed instruction, assess participants during research visit; perform initial review of study lab results; assess for any side effects or other problems; notify principal investigator of any participant reported side effects or problems.
- With detailed instruction, complete case report forms for each study participant, and document medical data in the patient record and sponsor database. Ensure case report forms or other data collection/tracking tools are created if not provided by sponsor.
- Assist PI with sponsor site visit and audits for assigned studies, including escorting visitors and providing requested documentation.
- Provides weekend and evening support for team coordination, communication, etc. to meet study protocol requirements.
Knowledge, Skills, and Abilities:
- Demonstrated excellence in written and verbal communication.
- Ability to interpret and analyze data.
- Demonstrated ability to collaborate effectively with peers, patients, management, and internal and external stakeholders, fostering professional relationships that support operational efficiency, patient-centered service, and cross-functional project success.
- Knowledge of the principles, practices and techniques of clinical research skills.
- Proven ability to provide high quality, compliant research and ethical standards.