What are the responsibilities and job description for the Infusion Nurse - PRN/Contract position at Wake Research?
Job Description
Job Description
Company Description
M3 Wake Research is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US. M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance.
Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000 successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.
We are looking for an Infusion Nurse to join our growing team. This position is an onsite, PRN position in Wilmington, NC .
Job Description
The Infusion Nurse performs critical trial-related procedures and makes important trial-related decisions when directed by the PI to do so. The Infusion Nurse is engaged in aspects of Investigational Product handling and has a significant role in the conduct of research. This position is primarily responsible for the accurate completion of Investigational Product dispensing and dosing, collection of information from study participants according to protocols, and for protecting the health, safety, and welfare of research participants. In addition, the Infusion Nurse may also act as the study coordinator for limited trials.
Essential Duties and Responsibilities :
Including, but not limited to the following :
- Performs activities related to Investigational product such as, but not limited to : handling and preparing, administration, and inventory management.
- Provides patient consultations and education in an outpatient setting under the direction of the physician in charge of the clinical trial.
- Reviews and adheres to assigned research study protocol.
- Maintains proper documentation and completes source documents in a timely manner.
- Ensures that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
- Collaborates with multidisciplinary team members and Sponsor / CRO / Vendor associates.
- Communicates with the participant as well as the participant’s partner / informant / caregiver.
- Attend and successfully complete all training programs; participate in ongoing conference calls, webinars, and other professional development opportunities.
- Complete provided training and Good Clinical Practice (GCP) training as required.
Qualifications
Education and Training Required :
Minimum Experience :
Additional Information
About M3USA
M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals and more. Since our inception in 2000, we’ve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems. Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements. Embrace the chance to drive change with M3 USA.
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