nurse researcher

Zucol Services Pvt. Ltd.

<p>Nursing Researcher &amp; Expert (Academic Content Writer)</p><p>The &ldquo;Nursing Researcher - Expert&rdquo; is supposed to do a good research and analysis to create the best Academic content for our International customers who are from different countries like The United States, United Kingdom, Australia, Germany, Singapore and many more. As a Nursing Researcher, you will get an opportunity to learn and experience the International education system and their academic environment of different countries.</p><p>Role and Responsibilities:</p><p>❖ Analyzing and understanding the customer&rsquo;s requirements.</p><p>❖ Conducting good research on customer&rsquo;s demand.</p><p>❖ Following the guidelines provided by the customer or reporting manager.</p><p>❖ Deliver quality content with No-Plagiarism.</p><p>❖ Completing work within the given deadlines.</p><p>❖ Following the rules and regulations of the company.</p><p>❖ Maintaining a good environment in the office.</p><p>❖ Addressing the changes or revisions as per the need of the customer.</p><p>Required Skills:</p><p>❖ Excellent communication and Interpersonal skills.</p><p>❖ Magnificent on English Grammar.</p><p>❖ Basic understanding of Biology, Nursing.</p><p>❖ Good command on Office365.</p><p>❖ Outstanding Multi-tasking skills.</p><p>❖ Ability to handle pressure.</p><p>Job Types: Full-time, Permanent, Fresher, Internship<br/>Contract length: 3-6 months</p><p>Pay: ₹15,000.00 - ₹18,000.00 per month</p><p>Work Location: In person</p>

Nursing researcher and Expert

Baylor College of Medicine

<div><div><div><div><h2 class="jobSectionHeader"><b>Summary</b></h2></div><div><p>
Baylor College of Medicine, Department of Pediatrics, Immunology, Allergy and Retrovirology Service at Texas Children&rsquo;s Hospital is seeking a highly motivated, responsible, and organized individual to join the HIV Research Program. We seek a professional nurse who possesses basic general knowledge of nursing practices, provides professional nursing skills involving Good Clinical Practice (GCP) in clinical research and is responsible for following procedures as described in research protocols and according to site and sponsor Standard Operating Procedures (SOPs). Duties include screening, enrolling participants, obtaining blood and other specimens for tests, administering medications, recording data for research analysis, and maintaining patient records. The nurse should ensure accurate data collection, documentation, and is responsible for organization and attention to safety for research visits.</p><p></p><p><br>
The Research Nurse I will be responsible for coordinating day to day activities for a number of research protocols in the HIV Research Program and especially in the Adolescent Trials Network. The ATN network, sponsored by the National Institutes of Health (NIH) addresses two critical pediatric HIV research questions:</p><ul><li>
The prevention of HIV in people from at-risk communities.</li><li>
The management of HIV infection in adolescents and young adults.</li></ul><p></p><p><br>
This position will be working with adolescents and young adults from the LGBTQ community and will need to provide culturally competent care.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Job Duties</b></h2></div><div><ul><li>
Documents clinical research data in electronic data capture (EDC).</li><li>
Answers queries in accordance with protocol requirements.</li><li>
Provides outreach in the community to enhance enrollment.</li><li>
Regularly provides updates, follow-ups on projects and ensures deadlines are met by all stakeholders as required.</li><li>
Works with Principal Investigator and CRA Regulatory Coordinator on both local, central and commercial Institutional Review Board (IRB) protocols, including but not limited to new protocol submission, amendments and renewals.</li><li>
Attends conference calls/answer emails as required by the study sponsor and relay the information to the study staff.</li><li>
May collect, process, ship, and maintain paperwork for blood and/or biological specimens according to procedures outlined in study protocol.</li><li>
Collects study specimens and check subjects&rsquo; vital signs.</li><li>
Performs study related procedures as outlined in the protocols such as administers questionnaires and conducts interviews.</li><li>
Performs responsibilities in a manner that promotes quality and safe patient care and customer service.</li><li>
Adheres to the scope of practices as defined by the Texas Nurse Practice Act.</li><li>
Recruits, screens, enrolls and evaluate patients that participate in NIH funded HIV research studies in children, adolescents and women.</li><li>
Schedules study visits and meetings related to studies.</li><li>
Administers study medications.</li><li>
Abstracts information from medical records according to the protocols.</li><li>
Ensures the clinical studies are conducted in accordance with guidelines of the FDA and other regulatory agencies.</li><li>
Educates patients in significant aspects of study.</li><li>
Serves as a liaison and distributes research information to faculty, research staff, principle investigator, and others as required.</li><li>
Maintains clean and safe work environment.</li><li>
Performs other duties as assigned.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Minimum Qualifications</b></h2></div><div><ul><li>
Associate's Degree or Bachelor's Degree in Nursing.</li><li>
No experience required.</li><li>
Current license as a Registered Nurse (RN) by the State of Texas Board of Nursing.</li><li>
Basic Life Support (BLS) Certification.</li></ul></div></div></div><p></p><p><b><br>
Work Authorization Requirement:</b></p><p><b>
This position is not eligible for visa sponsorship.</b> Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment.</p><p></p><p><br>
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.</p></div>

Research Nurse I

Randstad Technologies

<strong>Senior User Researcher (Contract)</strong><strong>The Role: Subject Matter Expert, User Researcher</strong> <p>We are seeking a highly experienced, independent <strong>Senior User Researcher</strong> for a key contract position. This is a strategic role where you will act as a <strong>Subject Matter Expert (SME)</strong>, driving optimal user experience across our digital products. You will be responsible for defining, executing, and synthesizing research that directly informs design and product strategy.</p> <p>This is a <strong>hybrid</strong> position requiring 3 days per week in our <strong> Newcastle</strong> office, working within a dynamic cross-functional environment.</p> <strong>Contract Details</strong> <p>This is a long-term contract opportunity requiring a hybrid presence in <strong> Newcastle</strong> (3 days in office). You will receive a generous <strong>holiday entitlement of 33 days (pro-rata)</strong>.</p> <strong>Key Responsibilities</strong> <p>As a Senior User Researcher, you will operate independently and champion the user voice by:</p> <ul> <li> <p><strong>Conducting End-to-End Research:</strong> Independently design, plan, and execute research using a wide array of methodologies, including in-depth user interviews, contextual inquiries, and usability testing.</p> </li><li> <p><strong>Applying Mixed-Methods Mastery:</strong> Utilizing <strong>Advanced Proficiency</strong> in both <strong>Qualitative Research</strong> and <strong>Quantitative Research</strong> (e.g., surveys, analytics, A/B testing) to deliver holistic, actionable insights.</p> </li><li> <p><strong>Creating Strategic Deliverables:</strong> Creating and maintaining critical user-centered artifacts, including detailed <strong>user personas</strong> and comprehensive <strong>journey maps</strong>, to align product strategy.</p> </li><li> <p><strong>Providing Design Guidance:</strong> Offering expert guidance to cross-functional teams, ensuring all design concepts and prototypes meet the requirements for <strong>Responsive and Adaptive Design</strong>.</p> </li><li> <p><strong>Stakeholder Advocacy:</strong> Actively participating in team discussions, presenting design concepts to stakeholders for review, and persuasively advocating for user needs and data-backed solutions.</p> </li><li> <p><strong>Demonstrating Tool Expertise:</strong> Showcasing <strong>Advanced proficiency in User Experience Research Tools and Techniques</strong> to streamline research operations and analysis.</p> </li></ul> <strong>What We're Looking For</strong> <p>You are a seasoned researcher with a proven track record of operating autonomously and providing strategic direction.</p> <strong>Essential Skills:</strong> <ul> <li> <p>Extensive professional experience as a Senior User Researcher, UX Researcher, or Product Researcher.</p> </li><li> <p>Demonstrated expertise in applying both <strong>Qualitative</strong> and <strong> Quantitative Research</strong> methods to drive product decisions.</p> </li><li> <p>Strong practical knowledge of research and design principles related to <strong> Responsive and Adaptive Design</strong>.</p> </li><li> <p>Exceptional ability to synthesize data from various sources into clear, impactful, and easily understood narratives.</p> </li><li> <p>Ability to act as an independent <strong>Subject Matter Expert</strong> and provide creative solutions to complex product problems.</p> </li><li> <p>Excellent collaboration and communication skills for working with Product, Design, and Engineering teams.</p> </li></ul> <strong>Mandatory Requirements:</strong> <ul> <li> <p>Availability to work in <strong>Newcastle</strong> on a hybrid basis (3 days in office).</p> </li><li> <p>Must be eligible to pass any necessary pre-employment background checks.</p> </li></ul> <p>Randstad Technologies is acting as an Employment Business in relation to this vacancy.</p>

User Researcher

Tennessee Oncology

<div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p>Tennessee Oncology, one of the nation&rsquo;s largest, community-based cancer care specialists, is home to one of the leading clinical trial networks in the country. Established 1976 in Nashville, Tennessee Oncology&rsquo;s mission remains unchanged: To provide access to high-quality cancer care and the expertise of clinical research for all patients, at convenient locations within their community and close to their home. Our growing network of physicians and locations is based on this mission. Tennessee Oncology is committed to advancing both the science of detection and targeted treatments, and to making these advances available to every patient. We believe caring for cancer patients is a privilege.</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p></p><p>
Why Join Us? We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.</p><p></p><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p><b>
Job Description:</b></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div><p>
As the Research Nurse for Tennessee Oncology your primary responsibility is to screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. You are responsible for source documentation and recording of adverse events. You are also responsible for dispensing oral investigational products and ensuring patient compliance with these medications</p><p><b>
ESSENTIAL FUNCTIONS:</b></p><ul><li>
You will be enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.</li><li>
Obtains and maintains informed consents of each patient for the duration of a study</li><li>
You will review the study design and inclusion/exclusion criteria with physician and patient.</li><li>
You will ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements.</li><li>
You will complete and document screening/eligibility accurately.</li><li>
You will complete and document the informed consent process accurately and has all parties sign/date as required, including HIPAA Authorization.</li><li>
You will accurately complete and submit on-study forms within required timelines</li><li>
You will document all specific tools required by the protocol (i.e., oral medication forms, pill count diaries, quality of life questionnaires, neuro exams, vital signs sheets, times of PK draws, etc.)</li><li>
You will screen every new patient or patient returning to office with scan results and document appropriately on the patient tracking logs</li><li>
You will ensure that patient documentation is completed at each clinic visit while in screening.</li><li>
You will ensure that all medications are approved prior to initiating treatment or when changing medication regimens, such as crossover studies.</li><li>
You will accurately calculate and document BSA, Creatinine Clearance, Urine Protein: Creatinine ratio, and any other calculations or conversions required per protocol.</li><li>
You will ensure that follow-up appointments, scans, or related procedures are scheduled correctly according to protocol requirements.</li><li>
You will document appropriately when patients are removed from protocol.</li><li>
You will ensure reconsent of patients at the next scheduled visit, following availability of updated ICF, and documents process appropriately</li><li>
provides patient education and medical information to study patients to ensure understanding or proper medication dosage, administration, and disease treatment.</li><li>
maintains medication inventory and reconciliation</li></ul><p></p><p><b>
KNOWLEDGE, SKILLS &amp; ABILITIES:</b></p><ul><li>
Knowledge of medical and research terminology</li><li>
Knowledge of FDA Code of Federal Regulations and GCP</li><li>
Knowledge of the clinical research processes</li><li>
At least one year of oncology experience, preferably hematology and/or transplant.</li><li>
At least one year of experience in a research setting preferred</li><li>
Research Certification (ACRP or CCRP) Preferred</li></ul><p></p><p><b>
EDUCATION &amp; EXPERIENCE:</b></p><ul><li>
An Associate Degree; preferably a bachelor&rsquo;s degree</li><li>
RN License</li></ul></div><p></p>

Research Nurse

Sarasota Memorial Health Care System

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 Research Institute
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  Job Summary
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   This position is fully on-site, no option for remote*
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 Responsible for the coordination and conduct of clinical trials, under the direction of the Principal Investigator and the Manager/Director, in accordance with the standards of good clinical practice and FDA regulations.
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 This position at our state of the art instutute is perfect for a well rounded clinical individual.
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  Required Qualifications
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 Require graduate of an accredited school of nursing or a diploma program. For new hires after 2012, Bachelor of Science Degree in nursing (BSN) is required within specified timeframe as outlined in the New Hire BSN Agreement policy (126.045).
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   Require certification as a Clinical Research Coordinator within one (1) year of eligibility.
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   Require appropriate training in Human Subject Protection and Safe Shipping/Handling of Bio-Hazardous Specimens (must be completed within thirty (30) days of hire.
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   Require a valid driver's license and the ability to drive to off-site locations.
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  Preferred Qualifications
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   Prefer knowledge of commonly used computer applications.
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   Prefer experience in a clinical research and/or a medical/surgical or critical care setting.
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   Prefer ability to initiate work without supervision.
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   Prefer demonstrated proficiency in interpersonal skills with staff, subjects, families, physicians, and sponsor/auditors of clinical trials.
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  Required License And Certs
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 BLS: Basic Life Support/CPR
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 FL RN: FL Registered Nurse License
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  Employment Screening Requirements
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 As part of Sarasota Memorial Health Care System&rsquo;s commitment to keeping people safe, all individuals providing care to vulnerable populations are required to undergo background screening through The Florida Care Provider Background Screening Clearinghouse. https://info.flclearinghouse.com/
</div>


Clinical Research Nurse (*on site position - no remote)*

SMA Legal

<p><b>Position:</b> Legal Researcher</p><p><b>Age Preference:</b> 22 to 26 years</p><p><b>Gender:</b> Neutral (Male or Female)</p><p><b>Minimum Qualification for a Legal Researcher:</b></p><ul><li>For a Legal Researcher: Master's Degree in Law (LLM), from a reputed University (preferably from an NLU)</li><li>Must be educated in English medium throughout</li></ul><p><b>Salary for Legal Researcher: </b>INR 25,000/- to INR 28,000/- per month</p><p><b>Location: </b>Candidate should be located in the Chandigarh tri-city area (Chandigarh UT, Mohali, or Panchkula)</p><p><b>Profession Competencies, Among Other Things:</b></p><ul><li>2-3 years' experience non-litigation, non-contentious firm (preferred)</li><li>Prior experience in Family Law, Company Law, Contract Law, among other areas of law</li><li>Excellent communication skills and command in English language</li><li>Familiarity in legal research databases</li><li>Very good knowledge of MS Office</li><li>Excellent organizational and multi-tasking abilities</li></ul><p><b>Key Deliverables, Among Other Things:</b></p><ul><li>Undertaking research in various areas of law, depending upon the work being actively carried out in the office and as required by the Managing Partner</li><li>Drafting of original research reports based upon research done</li><li>Undertaking a basic legal review of documents such as marriage certificates, birth certificates, passports, affidavits, etc. (for which requisite training will be provided)</li><li>Perform other office duties as assigned</li></ul><p><b>Employer's Description:</b></p><p>SMA Legal is a boutique Legal Advisory Firm that specializes in high profile cases involving Indian corporations, International companies with business interests in India, distinguished individuals and country missions to India.</p><p><b>Job Type:</b> Full-Time, Permanent</p><p><b>Ability to Commute/Relocate:</b></p><ul><li>Chandigarh: Reliably commute or planning to relocate before starting work (Preferred)</li></ul><p><b>Language Preferred: </b>English</p><p><b>Work Location: </b>In-person (Offline)</p><p>Job Types: Full-time, Permanent</p><p>Pay: ₹25,000.00 - ₹28,000.00 per month</p><p>Work Location: In person</p>

Legal Researcher

Fuse Energy

<p>We are currently seeking a quantitative researcher with a strong background in statistics to join our team. The role will be responsible for developing and implementing models for our energy supply business. As a quant researcher, you will work closely with our engineering team to ensure the accuracy and effectiveness of our models.</p> Responsibilities: <ul><li>Develop and implement models for our energy supply business using Python and other data science tools</li><li>Identify, analyze, and mitigate credit risk</li><li>Conduct data analysis and modeling to support risk management decisions</li><li>Stay current with industry developments and regulations related to credit risk management</li></ul> Requirements: <ul><li>2+ years of experience as a quantitative researcher or data scientist</li><li>Strong programming skills in Python and experience with data science tools such as Pandas, NumPy, and SciPy</li><li>Strong statistical and modeling skills</li><li>Strong communication and collaboration skills</li><li>Experience in the energy industry is a plus</li></ul> Benefits: <ul><li>Competitive salary and a stock options sign-on bonus</li><li>Biannual bonus scheme</li><li>Fully expensed tech to match your needs!</li><li>28 days paid annual leave per year including public holiday</li></ul>

Quantitative Researcher

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