Clinical Research Nurse- Full Time

Travel Required:

Clearance Required:

What You Will Do:
We are currently searching for a Research Nurse to provide support to the National Institutes of Health (NIH). This is primarily a clinical research role that will ensure human subjects' protections and patient-orientation during the course of the research subject’s participation in clinical research protocol. The role will assist with protocol development, implementation, and management including overseeing the collection of concise and verifiable data that contributes to public health. The role will perform duties in the following areas: protocol compliance, contributing as a co-investigator on clinical trials as well as various collaborative projects, adherence to ethical standards, informed consent, patient recruitment and retention, management of clinical trials patients, documentation and document management, data management and information technology, financial stewardship, and leadership and professional development. This is a full-time on-site opportunity located in Bethesda, MD.

• Assists in developing clinical research and protocol-specific standards of practice (SOP).

• Develops, implements, and assesses process improvement strategies for compliance with applicable regulations and SOPs.

• Develops and institutes a nursing feasibility review process to assess the ability to implement the protocol trial within local nursing care practices and standards.

• Collaborates with the principal investigator to finalize, ensure implementation, assess efficacy, and revise corrective and preventive action plans.

• Collaborates with PIs to resolve protocol implementation problems during design period; uses and revises/creates data capture forms to meet study needs.

• Directs the activities of multiple personnel involved in trials through clear delineation of responsibilities, endpoints, and approaches based on scope of practice and/or training.

• Assures compliance of clinical trial objectives and endpoints.

• Collaborates with health care members in the execution and management of trials; reports clinical data to regulator and monitoring agencies; and summarizes clinical data as requested by PIs.

• Works with principal investigators (PIs) and/or research programs to develop and implement interventions to provide education about misconduct to mitigate risk.

• Works with PIs and/or research programs to develop and reinforce a culture that facilitates compliance with reporting research misconduct.

• Develops supplemental materials for institutional review board (IRB) approval that assist in the informed consent process.

• Ensures compliance with consent for correlative studies by tracking the patient's wishes related to collection of associated specimens or data.

• Supports the informed consent process by continually providing patient/family counseling related to clinical trials and to the clinical trials process.

• Develops materials with input of PIs and IRB approval.

• Interviews and evaluates all patients being screened for entry into clinical trials.

• Develops study-specific materials for patient education and ensures IRB and sponsor approval, as required.

• Develops, implements, and assesses necessary interventions to address issues related to the patient population on a clinical trial.

• Interacts with physicians and web-based referral sources to assure that physicians and/or patients and their families receive answers to their questions and appropriate referral information in a timely manner.

• Collaborates with the interdisciplinary team to develop nursing practices that have the potential to improve patient outcomes.

• Implements plans to address identified trends related to noncompliance or deficiencies with source documents.

• Participates in the preparation of reports for appropriate regulatory agencies and monitoring bodies or boards.

• Assists the principal investigator in developing data management plans for each clinical trial.

• Uses information management and computer technology to support clinical data management activities.

• Assists in developing case reporting forms (CRFs) for multisite clinical trials.

• Participates in Quality Improvement and Quality Assurance (QA/QI) initiatives at the Section level; database and data system development efforts to produce consistency; and standardization and application of professional standards for gathering, storage, entry, reporting, and analysis of clinical trials data.

• Participates in ORSC-wide review of quality assurance/quality improvement and data entry procedures; direction of data management staff; and data entry and report generation activities designed to revise, plan, or upgrade data entry procedures.

• Anticipates and consistently meets reporting deadlines, collaborating with PIs and teams to note data trends and identify problems. Notes trends in toxicities, patient information, and data collection points.

• Verifies that routine care versus research-related cost descriptions in the protocol document match the consent document and vice versa. Ensures that the informed consent document identifies that stipends to patients for protocol-related activities are disclosed.

• Provides mentorship to new clinical trials nurses, research team members, and other healthcare providers.

• Disseminates information about the impact of new treatments and nursing practice. Participates in the development of publications related to clinical trials with focus on patient management and impact on current or future nursing practice.

• Participates in workgroups assessing problems impacting the clinical trial process, such as the revision of data collection tools, review of nursing concepts such as quality of life or pain relief, and educational initiatives.

What You Will Need:

• Bachelor’s degree in nursing (BSN) OR Associate’s degree in nursing (ADN) with TWO (2) additional years of experience in nursing, clinical, research, and/or related setting is equivalent to Bachelors.

• A minimum of TWO (2) years of experience in nursing, clinical, research, and/or related setting.

• Knowledge of environmental safety, including infection control, isolation technique, aseptic technique, and general security.

• Knowledge pertaining to privacy of the patient, privileged information, and secure handling of the patient’s medical records.

• Knowledge of federal regulatory requirements pertaining to clinical research

• Knowledge of Good Clinical Practice (GCP)

What Would Be Nice To Have:

• NIH clinical trials experience preferred.

What We Offer:

Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.

• Medical, Rx, Dental & Vision Insurance

• Personal and Family Sick Time & Company Paid Holidays

• Parental Leave

• 401(k) Retirement Plan

• Group Term Life and Travel Assistance

• Voluntary Life and AD&D Insurance

• Health Savings Account, Health Care & Dependent Care Flexible Spending Accounts

• Transit and Parking Commuter Benefits

• Short-Term & Long-Term Disability

• Tuition Reimbursement, Personal Development, Certifications & Learning Opportunities

• Employee Referral Program

• Corporate Sponsored Events & Community Outreach

• Care.com annual membership

• Employee Assistance Program

• Supplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.)