Clinical Research Nurse

Job Title: Clinical Research Registered Nurse This role focuses on the conduct of clinical trials within a clinical research unit, ensuring the safety and well-being of study participants while supporting the study team in the execution of research protocols. The Clinical Research Registered Nurse manages multiple projects, adheres to Good Clinical Practice standards, and provides direct clinical care alongside comprehensive data collection and documentation. Responsibilities

- Use effective time management techniques to manage multiple clinical research projects and ensure study objectives, timelines, and quality requirements are met.
- Read, understand, and execute assigned protocol tasks exactly as outlined in the study protocol.
- Perform angio-catheter placement for blood sampling and intravenous medication administration in accordance with clinical and protocol standards.
- Oversee and perform data collection in strict alignment with Standard Operating Procedures, study protocols, and Good Clinical Practice (GCP) guidelines.
- Obtain required blood samples through angio-catheters and direct venipuncture while maintaining subject comfort and safety.
- Collect biological samples including urine, feces, and timed urine collections as specified by study protocols.
- Measure and record vital signs such as blood pressure, heart rate, and temperature at protocol-defined time points.
- Obtain and document medical histories, height, and weight of study participants accurately and thoroughly.
- Perform and interpret electrocardiograms (ECGs) as required by the clinical trial protocols.
- Monitor, document, and manage adverse events through detailed clinical observations and timely reporting.
- Monitor and document concomitant medications taken by study participants throughout trial participation.
- Provide comprehensive clinical care to subjects during study participation, ensuring their safety and well-being.
- Monitor the activities of Medical Assistants, Licensed Practical Nurses (LPNs), and Study Assistants to ensure adherence to study procedures and quality standards.
- Complete case report forms (CRFs) accurately and in a timely manner, ensuring high-quality data entry and integrity.
- Perform emergency and resuscitative interventions when appropriate and in accordance with clinical guidelines and training.
- Assist in the training, onboarding, and mentoring of new clinical research personnel to promote consistency and quality in study conduct.
- Provide leadership within the clinical research unit in the absence of the Study Coordinator, supporting workflow and decision-making.
- Participate actively in patient pre-screening and chart review to assess eligibility for clinical trials.
- Support patient recruitment activities by engaging potential participants and explaining study procedures and requirements.
- Collaborate closely with the broader study team on all functions related to protocol execution, safety monitoring, and data quality.

Essential Skills

- Current Registered Nurse (RN) license in New York or New Jersey.
- Ability to manage multiple clinical research projects using effective time management techniques.
- Proficiency in reading, understanding, and executing clinical trial protocols.
- Hands-on experience with angio-catheter placement for blood sampling and intravenous medication administration.
- Strong skills in venipuncture and collection of blood samples.
- Competence in collecting urine, feces, and timed urine specimens according to protocol requirements.
- Ability to obtain and accurately record vital signs, including blood pressure, heart rate, and temperature.
- Experience in obtaining and documenting medical history, height, and weight of patients.
- Capability to perform electrocardiograms (ECGs) and document findings.
- Knowledge of monitoring and documenting adverse events based on clinical observations.
- Experience in monitoring and recording concomitant medications during clinical trials.
- Clinical skills to provide direct patient care to subjects during study participation.
- Ability to oversee and guide Medical Assistants, LPNs, and Study Assistants in daily study activities.
- Strong attention to detail for accurate and timely completion of case report forms (CRFs).
- Training and competence in emergency response and resuscitative interventions.
- Working knowledge of Good Clinical Practice (GCP) standards and their application in clinical research.
- Experience in clinical research, including participation in the conduct of clinical trials.
- Ability to contribute to patient pre-screening, chart review, and patient recruitment for studies.

Additional Skills & Qualifications

- Bachelor of Science in Nursing (BSN) is preferred.
- Experience in patient pre-screening and eligibility assessment for clinical trials.
- Background in chart review for research or clinical purposes.
- Familiarity with patient recruitment strategies and processes in a research setting.
- Experience assisting study teams with protocol execution, safety monitoring, and data collection.
- Ability to train, mentor, and support new personnel in a clinical research environment.
- Demonstrated leadership capability within a clinical or research unit.

Work Environment The position is based in a clinical research unit that conducts regulated clinical trials in accordance with Standard Operating Procedures, study protocols, and Good Clinical Practice guidelines. The environment is highly collaborative, with close interaction among Registered Nurses, Medical Assistants, Licensed Practical Nurses, Study Assistants, and study coordinators. Work involves direct patient contact, frequent collection of biological samples, performance of electrocardiograms, and continuous monitoring of vital signs and clinical status. The role may require flexibility in scheduling to meet protocol-specific visit windows and timed sample collections. Professional clinical attire is expected to maintain a safe, clean, and respectful environment for study participants and staff.
Job Type & Location
This is a Permanent position based out of Eatontown, NJ.
Pay and Benefits
The pay range for this position is $93600.00 - $104000.00/yr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Clinical Research Nurse: Clinilabs Internal Perm Benefits
Job Type & Location
This is a Permanent position based out of Eatontown, NJ.
Application Deadline
This position is anticipated to close on Oct 26, 2026.
Workplace Type
This is a fully onsite position in Eatontown,NJ. About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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