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Travel Nurse
3 months ago
at ClinChoice (View all jobs)
Pennsylvania
ClinChoice is searching for a Travel Nurse, the candidate must be a licensed registered nurse to work on a long-term medical device study (approximately 2 years). This role will average 10-20 hours per month. It requires travel to the hospital sites in PA, NY and TX (total of 7 sites). The Clinical Research Nurse will play an important role in irrigations, training on use of device and presence in the operating room. The nurse will also be responsible for regulatory documents, data collection, and facilitation of meetings to serve as the main point of contact for the overall coordination of the clinical trial. This position requires a nurse with surgical experience who is comfortable working in a dynamic and travel-intensive environment.
The preference is for candidates to be self-employed, 1099 employees. However, if you are interested in the role and prefer w-2 employment please let us know. The procedures are scheduled far in advance so you will know your schedule weeks ahead.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts.
Main Job Tasks and Responsibilities:
Surgical Support:
Presence in the Operating Room (OR): Provide direct support during surgical procedures, including assisting with the use of medical devices and ensuring sterile conditions are maintained. Device Setup and Assistance: Assist in the setup and operation of specialized devices used in the study, ensuring proper functioning and adherence to protocols. Collaboration with Surgical Teams: Work closely with surgeons, anesthesiologists, and other OR personnel to ensure smooth surgical workflows and patient safety.
Irrigations:
Conducting Irrigations: Perform irrigation procedures as required by the study protocol, ensuring precise and consistent application. Documentation: Accurately document all irrigation procedures, including patient responses and any deviations from the protocol.
Training and Education:
Device Training: Provide comprehensive training to healthcare providers on the proper use and maintenance of study devices, ensuring understanding and compliance. Patient Education: Educate patients and their families on the study procedures, device usage, and post-operative care.
Compliance and Protocol Adherence:
Protocol Compliance: Ensure all study procedures are conducted in accordance with the study protocol, regulatory requirements, and ethical standards. Data Collection: Collect and document study data accurately and timely, adhering to study timelines and quality standards.
Travel Requirements:
Travel to various clinical sites as required by the study schedule. Flexibility to adapt to changing locations and schedules is essential.
Accommodation and Logistics:
Coordinate travel logistics, including accommodations and transportation, in collaboration with the study team.
Additional Responsibilities:
Direct the activities of professionals engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. Ensure compliance with each study’s protocol by providing thorough review and documentation at each subject study visit. Administer investigational products and performs patient assessments during clinical visits to determine the presence of side effects; notifies Principal Investigator of findings/issues. Provides patient education and medical information to study patients to ensure understanding of proper investigational produce use, administration, and disease treatment. Documents medical data in the patient charts to capture protocol requirements. Schedule site visits. Monitors study activities to ensure compliance with protocols and with relevant local, federal and state regulatory and institutional policies. Maintains required records of patient performance and ability to use device. Records adverse event and side effect data and confers with investigators regarding the reporting of events to oversight agencies. Prepares for or participates in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. Identifies protocol problems, informs investigators of problems, or assists in problem resolution efforts such as protocol revisions.
Education, Experience and Skills:
Minimum of a diploma from an accredited nursing school required; Bachelor of Nursing or other Science degree preferred. Three years of recent clinical nursing experience in a hospital, clinic, or similar health care setting. 1 year in a surgical setting preferred. Experience with clinical research or device studies is a plus. Nursing competency skills per scope of practice, including surgical experience, performing vital signs, nursing assessments, performing ECG/EKG, administering injections, etc. At least one year of clinical trials research experience is preferred but not required. Medical Device study experience (beneficial). Experience using Electronic Data Capture (EDC) systems. Experience facilitating IRB submissions. Experience with site budget review. Must have a GCP certification. Training will be provided. Knowledge of biological and medical terminology. Understanding of the principles of administration and management. Detail-orientated and meticulous in all aspects of work. Strong attention to detail, proactively identifying and solving problems; ability to demonstrate initiative. Proficiency in Microsoft Office (e.g., Word, Excel, Outlook). Must be able to lift 15 pounds at a time.
Education, Experience and Skills:
Minimum of a diploma from an accredited nursing school required; Bachelor of Nursing or other Science degree preferred. Three years of recent clinical nursing experience in a hospital, clinic, or similar health care setting. 1 year in a surgical setting preferred. Experience with clinical research or device studies is a plus. Available to work 10-20 hours/week and available to travel to locations NY, TX, PA a total of 7 sites. Nursing competency skills per scope of practice, including surgical experience, performing vital signs, nursing assessments, performing ECG/EKG, administering injections, etc. At least one year of clinical trials research experience is preferred but not required. Medical Device study experience (beneficial). Experience using Electronic Data Capture (EDC) systems. Experience facilitating IRB submissions. Experience with site budget review. Must have a GCP certification. Training will be provided. Knowledge of biological and medical terminology. Understanding of the principles of administration and management. Detail-orientated and meticulous in all aspects of work. Strong attention to detail, proactively identifying and solving problems; ability to demonstrate initiative. Proficiency in Microsoft Office (e.g., Word, Excel, Outlook). Must be able to lift 15 pounds at a time.
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
Key Words: Clinical Trial Study Nurse, Study Nurse, Irrigations, RN, FSP, clinical studies, Registered Nurse, clinical trials, medical devices, travel nurse, operating room
#LI-VH1 #LI-Remote #Associate #Parttime
The base salary pay range represents the anticipated low and high range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
Pay Range
$48 — $48 USD
