Research Nurse (Per Diem) - Fort Wayne, IN
Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries.
Posted Sep 24
- License
- RN license
- Term
- Per Diem Research Nurse (Per Diem) - Fort Wayne, IN
Do you qualify?
- Certification
- GCP certification Research and clinical trials experience with GCP certification.
- Experience
- 2 years' post qualification experience Registered nurse with a minimum of 2 years' post qualification experience.
- Experience
- Research and clinical trials experience
- Also asks
- ability to work autonomously with initiative in a team within a multidisciplinary environment Ability to work autonomously with initiative in a team within a multidisciplinary environment.
- Also asks
- verbal and written communication skills Excellent verbal and written communication skills.
- Also asks
- ability to prioritize and manage multiple tasks Ability to prioritize and manage multiple tasks.
- Also asks
- working knowledge of computer software including Outlook, Word, Excel, and PowerPoint Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum.
Preferred
- Experience
- clinical nursing skills such as Venepuncture and ECG Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable.
- Also asks
- knowledge of research design and methodology Knowledge of research design and methodology desirable.
What it pays
- Against similar roles
- Indiana PRN median is $89k/yrIndiana PRN postings that state pay run $49k/yr to $108k/yr, the middle half $66k/yr to $100k/yr, across 70 postings. This posting's $68k/yr to $115k/yr is wider than that, so where you land depends on the offer.
- Bonus
- commissions/bonus Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time.based on company and individual performance
- Pay reviews
- actual salary varies based on candidate's qualifications, skills, competencies, and proficiency
Benefits
- Benefitscompany car or car allowance
- BenefitsMedical, Dental and Vision
- BenefitsCompany match 401k
- BenefitsEmployee Stock Purchase Plan
- Benefitsflexible paid time off (PTO) and sick timeflexible paid time off (PTO) and sick time.
- Medical
More benefits (4)
- Dental
- Vision
- PTO
- Sick time
The role and schedule
- Day to day
- conversant with trial protocol, CRFs/eCRF, off-site manual, procedures, timelines, and SOPs
- Day to day
- communicate with research nurse project manager, manager, site staff, and PI
- Day to day
- maintain accurate documentation and electronic data transfer per SOPs and GCP
- Day to day
- attend Site Initiation Visits and project meetings Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi- disciplinary, project management and client-facing meetings.
- Day to day
- coordinate and complete subject trial visits on- and off-site
- Day to day
- administer trial medication and facilitate safe storage, transfer, and accountability Administer trial medication as per the protocol, and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs.
- Day to day
- process, package, and dispatch samples with couriers Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents.
- Day to day
- assist in identifying and recruiting eligible patients for clinical trials
- Day to day
- report adverse events, SAEs, and SUSARs to site team and RNPM
- Day to day
- report suspected misconduct or fraud Report any suspected misconduct or fraud to Illingworth and associated companies.
- Travel
- on- and off-site subject trial visits Coordinate (working with the RN team) and complete subject trial visits on- and off-site.
The workplace
Your fit
Questions to ask
- Can you walk me through the pay period for the posted pay range and differentials?
- What should I expect for shifts, weekly hours, weekend, holiday, call, and rotation?
- What orientation, preceptor time, and ongoing unit support are included?
- How are patient load, floating, and staffing support handled day to day?
Original listing
Read full textShow less
Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. These include mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth are experts with experience across all study phases and in a diverse range of therapeutic areas.
Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives.
Job Responsibilities
- Fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable day to day running of the trial including all relevant SOPs.
- Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff and the Principal Investigator, to ensure a smooth and efficient flow of information.
- Maintain accurate documentation including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements.
- Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi- disciplinary, project management and client-facing meetings.
- Coordinate (working with the RN team) and complete subject trial visits on- and off-site. Ensure all trial related procedures and assessments are completed according to the protocol and relevant SOPs and that data is collected accurately.
- Administer trial medication as per the protocol, and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs.
- Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents.
- Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials providing information and support for those patients for on- and off-site care.
- Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required.
- Report any suspected misconduct or fraud to Illingworth and associated companies.
Qualifications
- Registered nurse with a minimum of 2 years' post qualification experience.
- Research and clinical trials experience with GCP certification.
- Knowledge of research design and methodology desirable.
- Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable.
- Ability to work autonomously with initiative in a team within a multidisciplinary environment.
- Excellent verbal and written communication skills.
- Ability to prioritize and manage multiple tasks.
- Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum.
At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time.
Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.
Salary Range
$67,700.00 - $115,100.00
The base salary range represents the anticipated low and high of the Syneos Health 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.
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description.
The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms.
Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
What's around it?
Indiana
Living costs about 7% below the US average