6 Research Nurse Job Description Templates and Examples

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are looking for a detail-oriented Junior Research Nurse to join our innovative research team. In this role, you will support clinical trials by assisting in the coordination and execution of research protocols while ensuring compliance with regulatory requirements. You will play a crucial part in facilitating patient recruitment and data collection, contributing to advancements in medical research.

Responsibilities

• Assist in the recruitment and screening of study participants, ensuring eligibility criteria are met
• Conduct clinical assessments and collect data following research protocols
• Maintain accurate and detailed records of research activities and participant interactions
• Collaborate with senior research staff to ensure compliance with ethical and regulatory standards
• Provide support during site visits and monitor participant safety throughout the study
• Participate in team meetings to discuss study progress and contribute to problem-solving efforts

Required and Preferred Qualifications

Required:

• Registered Nurse (RN) with a current nursing license
• 1+ years of clinical nursing experience, preferably in a research or clinical trial setting
• Strong organizational skills with attention to detail
• Excellent communication skills, both verbal and written

Preferred:

• Bachelor’s degree in Nursing or a related field
• Experience with electronic data capture systems
• Knowledge of Good Clinical Practice (GCP) guidelines

Technical Skills and Relevant Technologies

• Proficiency in clinical documentation and data management systems
• Familiarity with medical terminology and clinical trial processes
• Experience with patient management software is a plus

Soft Skills and Cultural Fit

• Strong interpersonal skills with the ability to work collaboratively in a team environment
• Adaptable and able to thrive in a fast-paced research setting
• Commitment to patient-centered care and ethical research practices
• Proactive problem solver with a focus on continuous improvement

Benefits and Perks

Salary: [$SALARY_RANGE]

Full-time offers include:

• Comprehensive health benefits
• Flexible work hours and remote work options
• Professional development opportunities and tuition reimbursement
• Generous paid time off and holidays

Equal Opportunity Statement

[$COMPANY_NAME] is committed to diversity in its workforce and is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation or any other basis protected by applicable law.

Location

This is a fully remote position.

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are seeking a dedicated and detail-oriented Research Nurse to join our research team. In this fully remote position, you will play a vital role in the clinical research process by providing nursing support for clinical trials, ensuring the safety and well-being of participants, and facilitating compliance with regulatory requirements.

Responsibilities

• Conduct clinical assessments and evaluations of study participants to monitor their health and eligibility for research protocols.
• Administer medications and treatments as prescribed during clinical trials, ensuring adherence to study protocols.
• Collect and document clinical data accurately, maintaining high standards of quality and integrity in research records.
• Provide education and support to study participants regarding the research process, potential risks, and benefits of participation.
• Collaborate with multidisciplinary teams to develop and implement study protocols, ensuring compliance with regulatory and ethical standards.
• Participate in the development of recruitment strategies and assist in the enrollment of study participants.
• Monitor adverse events and report findings to the principal investigator and regulatory bodies as necessary.
• Stay current with the latest research developments and clinical practices relevant to the studies being conducted.

Required and Preferred Qualifications

Required:

• Registered Nurse (RN) license in good standing.
• Bachelor’s degree in Nursing or a related field.
• 2+ years of clinical nursing experience, preferably in a research or clinical trial setting.
• Strong understanding of clinical research regulations and Good Clinical Practice (GCP) guidelines.
• Excellent communication and interpersonal skills, with the ability to build rapport with participants and team members.

Preferred:

• Certification in Clinical Research (ACRP or SOCRA).
• Experience in patient recruitment and retention strategies.
• Proficiency with electronic data capture systems and clinical trial management software.

Technical Skills and Relevant Technologies

• Familiarity with clinical trial protocols and regulatory requirements.
• Strong organizational skills and attention to detail for managing clinical documentation.
• Proficiency in Microsoft Office Suite and clinical data management systems.

Soft Skills and Cultural Fit

• Empathetic and compassionate approach towards patient care and participant safety.
• Ability to work independently in a remote setting while managing multiple priorities.
• Strong problem-solving skills and adaptability in a dynamic research environment.
• Commitment to continuous learning and professional development in clinical research.

Benefits and Perks

Annual salary range: [$SALARY_RANGE]

Full-time employees may enjoy:

• Comprehensive health, dental, and vision insurance.
• Flexible work hours and a fully remote work environment.
• Generous paid time off and holidays.
• Retirement savings plan with company matching.
• Continuing education opportunities and professional development support.

Equal Opportunity Statement

[$COMPANY_NAME] is committed to fostering a diverse and inclusive workplace. We welcome applicants from all backgrounds and walks of life, and we encourage applications from individuals with diverse experiences and perspectives. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or veteran status.

Location

This is a fully remote position.

Note: We encourage applicants to apply even if they do not meet all the specified qualifications. Your unique experiences and perspectives may be valuable to our team.

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are seeking a highly skilled and motivated Senior Research Nurse to join our clinical research team. In this role, you will play a critical part in advancing medical knowledge and improving patient care through the execution of clinical trials. You'll leverage your clinical expertise and research acumen to ensure the highest standards of care and adherence to protocol across multiple studies.

Responsibilities

• Lead the clinical management of research participants, ensuring informed consent processes are thorough and ethical.
• Collaborate with multidisciplinary teams to design, implement, and monitor clinical trial protocols, while ensuring compliance with regulatory requirements.
• Conduct comprehensive assessments of participant health, including physical examinations, laboratory tests, and medication administration.
• Provide education and support to research participants, answering questions and addressing concerns to optimize participant retention and engagement.
• Analyze and document participant data, ensuring accuracy and integrity while adhering to Good Clinical Practice (GCP) standards.
• Mentor and train junior research nurses and staff on best practices and protocols to foster a culture of continuous learning and improvement.

Required and Preferred Qualifications

Required:

• Registered Nurse (RN) with a current nursing license and a minimum of 5 years of clinical nursing experience.
• Demonstrated experience in clinical research, including knowledge of research methodologies and regulatory requirements.
• Strong understanding of GCP guidelines and ethical considerations in clinical trials.
• Proficiency in electronic data capture systems and clinical trial management software.

Preferred:

• Master's degree in Nursing, Public Health, or a related field.
• Certification in Clinical Research (e.g., ACRP or SOCRA certification).
• Experience in specific therapeutic areas relevant to ongoing clinical trials.

Technical Skills and Relevant Technologies

• Proficient in using electronic health records (EHR) and clinical trial management systems (CTMS).
• Familiarity with statistical analysis software and data management tools.
• Knowledge of patient safety regulations and clinical trial risk management.

Soft Skills and Cultural Fit

• Exceptional communication and interpersonal skills, with the ability to build rapport with diverse populations.
• Strong organizational and time management abilities, capable of managing multiple projects simultaneously.
• A proactive and detail-oriented mindset, with a commitment to patient safety and quality care.
• Ability to thrive in a fast-paced, remote work environment while maintaining a collaborative team spirit.

Benefits and Perks

Salary range: [$SALARY_RANGE]

We offer a comprehensive benefits package that may include:

• Flexible work arrangements with a fully remote work environment.
• Health, dental, and vision insurance with competitive premiums.
• Generous paid time off (PTO) policy and paid holidays.
• Professional development opportunities and support for continuing education.
• Retirement savings plan with company match.

Equal Opportunity Statement

[$COMPANY_NAME] is committed to creating a diverse environment and is proud to be an Equal Opportunity Employer. We encourage all qualified applicants to apply regardless of race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Location

This is a fully remote position.

Note: By submitting your application, you acknowledge and agree to our data processing terms as outlined in our Global Data Privacy Notice for Job Candidates and Applicants.

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are seeking a highly skilled Lead Research Nurse to join our esteemed clinical research team at [$COMPANY_NAME]. This individual will play a pivotal role in overseeing nursing activities related to clinical trials, ensuring compliance with regulatory standards, and facilitating high-quality patient care throughout the research process.

Responsibilities

• Lead and coordinate nursing staff in the execution of clinical research protocols, ensuring adherence to Good Clinical Practice (GCP) and other regulatory requirements.
• Collaborate with principal investigators and clinical research coordinators to design, implement, and evaluate clinical trials.
• Monitor patients' health status and respond to any adverse reactions or complications during clinical trials, ensuring patient safety and well-being.
• Provide training and mentorship to nursing staff and coordinate nursing activities, fostering a culture of continuous improvement.
• Maintain accurate documentation and reporting of clinical trial data, including patient assessments and treatment outcomes.
• Act as a liaison between research teams and institutional review boards (IRBs) to ensure the ethical conduct of research.

Required and Preferred Qualifications

Required:

• Registered Nurse (RN) with a current license in [$COMPANY_LOCATION].
• 5+ years of clinical nursing experience, including at least 2 years in a research or clinical trial setting.
• Strong knowledge of clinical trial protocols and regulatory requirements.
• Exceptional organizational skills with the ability to manage multiple projects simultaneously.

Preferred:

• Bachelor’s degree in Nursing (BSN) or higher.
• Certification in Clinical Research (e.g., ACRP or SOCRA).
• Experience in a specific therapeutic area relevant to the research conducted at [$COMPANY_NAME].

Technical Skills and Relevant Technologies

• Proficient in Electronic Data Capture (EDC) systems and clinical trial management software.
• Ability to utilize medical software for patient management and documentation.
• Familiarity with data analysis tools and methodologies used in clinical research.

Soft Skills and Cultural Fit

• Excellent communication and interpersonal skills, with the ability to collaborate effectively with multidisciplinary teams.
• Strong critical thinking and problem-solving abilities, particularly in fast-paced and dynamic environments.
• Demonstrated leadership skills with a passion for mentoring and developing nursing staff.
• A commitment to ethical practice and patient-centered care.

Benefits and Perks

We offer a competitive salary and a comprehensive benefits package, including:

• Health, dental, and vision insurance.
• Retirement plans with company matching.
• Generous paid time off and holiday schedule.
• Continuing education reimbursement.
• Opportunities for professional development and advancement within the organization.

Equal Opportunity Statement

[$COMPANY_NAME] is committed to diversity and inclusion in the workplace. We are proud to be an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation, or any other basis protected by applicable law.

Location

This role requires successful candidates to be based in-person at our facility located in [$COMPANY_LOCATION].

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are looking for a detail-oriented and motivated Clinical Research Coordinator to join our dynamic research team at [$COMPANY_NAME]. This role is essential in managing and overseeing clinical trials, ensuring compliance with regulatory requirements, and facilitating communication between multiple stakeholders. You will play a key role in advancing our research initiatives while contributing to groundbreaking developments in the healthcare sector.

Responsibilities

• Coordinate all aspects of clinical trials, including budgeting, scheduling, and recruitment of study participants
• Ensure adherence to study protocols, regulatory guidelines, and ethical standards throughout the research process
• Collaborate with Principal Investigators and study teams to develop and implement study protocols
• Monitor and document trial progress, including data collection, participant follow-up, and adverse event reporting
• Conduct training sessions for research staff on study protocols and regulatory compliance
• Act as a liaison between sponsors, regulatory agencies, and other external stakeholders
• Prepare and submit regulatory documents, including IRB submissions and study reports

Required and Preferred Qualifications

Required:

• Bachelor’s degree in life sciences, nursing, or a related field
• 2+ years of experience in clinical research coordination or a similar role
• Strong understanding of Good Clinical Practice (GCP) and regulatory requirements
• Excellent organizational and multitasking skills with a keen attention to detail
• Proficient in data management and clinical trial management systems

Preferred:

• Certification in Clinical Research (e.g., ACRP, SOCRA) is a plus
• Experience with electronic data capture (EDC) systems and clinical trial software
• Knowledge of statistical analysis and data interpretation

Technical Skills and Relevant Technologies

• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint) and research management software
• Familiarity with data analysis tools (e.g., SPSS, SAS) is advantageous
• Experience with EHR systems and patient management databases

Soft Skills and Cultural Fit

• Strong interpersonal and communication skills, both written and verbal
• Ability to work collaboratively in a team-oriented environment
• Proactive problem-solving skills and a strong sense of accountability
• Adaptability in a fast-paced research environment with changing priorities
• Commitment to ethical practices and continuous improvement in research

Benefits and Perks

We offer a competitive salary and a comprehensive benefits package that includes:

• Health, dental, and vision insurance
• 401(k) retirement plan with company match
• Generous paid time off and holiday schedule
• Ongoing professional development opportunities
• Supportive work environment fostering growth and innovation

Equal Opportunity Statement

[$COMPANY_NAME] is an Equal Opportunity Employer, committed to fostering an inclusive workplace. We celebrate diversity and are dedicated to creating a welcoming environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, veteran status, or any other characteristic protected by law.

Location

This role requires successful candidates to be based in-person at our headquarters in [$COMPANY_LOCATION].

We encourage applicants from diverse backgrounds and experiences to apply, even if they do not meet all the specified qualifications. Your unique perspective may be exactly what we need.

Company Overview

[$COMPANY_OVERVIEW]

Role Overview

We are seeking a highly skilled Clinical Research Manager to lead our clinical trial operations at [$COMPANY_NAME]. This role is critical in driving the development and execution of innovative clinical research protocols while ensuring compliance with regulatory standards and promoting the highest quality of scientific integrity.

Responsibilities

• Oversee the planning, execution, and management of clinical trials from initiation to completion, ensuring adherence to timelines and budgets.
• Lead cross-functional teams to develop robust clinical study protocols and ensure effective implementation of study procedures.
• Establish and maintain relationships with key stakeholders, including investigators, site coordinators, and regulatory bodies.
• Ensure compliance with Good Clinical Practice (GCP), local regulations, and company policies throughout the clinical trial process.
• Provide training and mentorship to clinical research staff to enhance their skills and ensure consistency in trial execution.
• Monitor trial progress and manage issues that may arise, implementing corrective actions as necessary.
• Prepare and present study updates to internal and external stakeholders, ensuring transparency and accountability in all research activities.

Required and Preferred Qualifications

Required:

• Master’s degree in a relevant field (e.g., Life Sciences, Nursing, Public Health) or equivalent work experience.
• 5+ years of experience in clinical research, including experience in managing clinical trials.
• Strong understanding of clinical research methodologies, regulatory requirements, and GCP.
• Proven ability to lead and motivate cross-functional teams in a fast-paced environment.
• Excellent organizational, analytical, and problem-solving skills.

Preferred:

• PhD or equivalent in a relevant field.
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Previous experience in a therapeutic area relevant to our research focus.

Technical Skills and Relevant Technologies

• Deep expertise in clinical trial design and execution methodologies.
• Proficiency in data analysis tools and statistical software.
• Familiarity with regulatory submissions and documentation processes.

Soft Skills and Cultural Fit

• Exceptional communication and interpersonal skills for effective collaboration with diverse teams.
• Strong commitment to ethical standards and scientific rigor in all research activities.
• A proactive approach to problem-solving, with a focus on driving results.
• Ability to thrive in a dynamic, fast-paced environment while managing multiple priorities.

Benefits and Perks

Annual salary range: [$SALARY_RANGE]

In addition, we offer a comprehensive benefits package that may include:

• Health, dental, and vision insurance
• Retirement plans with company matching
• Generous paid time off and holidays
• Professional development opportunities and resources
• Collaborative and inclusive work environment

Equal Opportunity Statement

[$COMPANY_NAME] is committed to creating a diverse environment and is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, sex, gender expression or identity, sexual orientation or any other basis protected by applicable law.

Location

This role requires successful candidates to be based in-person at our facility located in [$COMPANY_LOCATION].

We encourage applicants who may not meet every qualification listed to apply, as we value diverse experiences and perspectives.