Who we are

The opportunity

The Clinical Research Nurse is responsible for:

• Providing ongoing assessment of the study subject/patient to identify Adverse Events (AEs), ensures proper documentation and reporting of all AEs, including follow up of open AEs when subjects are not in-house, and providing any appropriate clinical care or instructions to subjects, as directed by the PI or as deemed medically necessary by their professional judgment.
• Conducting procedures in strict compliance to the study protocol, Good Clinical Practice standards, Standard Operating Procedures (SOP’s), QA/QC procedures, OSHA guidelines and other state and local regulations as applicable.
• Assisting the PI with the review of laboratory data results for both the selection and randomization of study participants and for the monitoring of safety parameters.
• Communicating the progress of study conduct to PI, CSM, and members of the clinical study team.
• Managing and monitoring the well-being and safety of study participants by active assessment and by serving as a visible point of contact at all times.
• Facilitating verbal directions from the Principal Investigator (PI) to study participants and/or clinical study staff and ensuring appropriate follow-through.
• Notifying the PI, CSM, and members of the clinic management team upon the occurrence or reporting of a Serious Adverse Event (SAE) by a study participant and initiating documentation of the event.

This is a floating position with fluctuating hours including weekends.

How you’ll spend your day

• Providing administrative and operational support to ensure successful conduct of study protocols.
• Performing as the floor leader and mentor, assisting research technicians, paramedics, and laboratory technicians. (In the absence of the Clinical Study Manager.)
• Maintaining compliant, clear and accurate study charts and documentation of all AEs reported and Concomitant Medication usage throughout the study.
• Reinforcing rules and regulations with study participants, managing participant complaints, and maintaining participant satisfaction.
• Working with CSM and Training Manager to provide protocol training to the clinical study team, as well as to communicating on-the-spot performance direction and feedback as needed.
• Administering study medication according to study protocol, demonstrating a thorough understanding of study medications, administering concomitant medication as directed by the PI, and maintaining accurate and timely documentation.
• Managing the completion of all End of Study or Early Termination activities by study participants, inclusive of follow up for the close-out of any outstanding items (i.e. AEs, physical exams, lab repeats, etc.) after subjects have been discharged from the clinic.
• Providing leadership to the clinical study team.

Your experience and qualifications

• Nursing degree.
• In-state license.

Enjoy a more rewarding choice

Make a difference with Teva Pharmaceuticals

Reports To

Manager of Clinic Operations

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Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

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