Clinical Research Coordinator, Registered Nurse

MidLantic Urology; Lancaster (Lancaster County); On-site; USD 60,000 - 80,000; Full time

Job summary

MidLantic Urology is seeking a Clinical Research Coordinator, Registered Nurse to manage clinical trials in a supportive environment. The role involves study coordination, regulatory compliance, and patient advocacy, offering a chance to participate in impactful research. Competitive pay and benefits are provided.

Benefits

Health insurance

Vision insurance

Life Insurance

Pet Insurance

Health savings account

Paid time off

Paid holidays

Profit sharing

Free parking

Qualifications

• Must be a Registered Nurse (RN) with a current and valid license.
• 2 or more years of Nursing experience in relevant fields preferred.

Responsibilities

• Responsible for managing subject recruitment and enrollment for clinical trials.
• Ensure compliance with protocols and regulatory requirements.
• Maintain good documentation practices for clinical trial activities.

Skills

Excellent verbal and written communication skills

Ability to draw blood

Understanding of biomedical research protocols

Organizational skills

Ability to start IVs and administer medications

Education

Associate’s or Bachelor’s degree in Nursing (ASN or BSN)

Job description

Clinical Research Coordinator, Registered Nurse

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Clinical Research Coordinator, Registered Nurse

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This range is provided by MidLantic Urology. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$37.00/hr - $45.00/hr

Direct message the job poster from MidLantic Urology

Talent Acquisition Manager at Solaris Health | HR Leader with Recruitment Expertise

Work Location: 2106 Harrisburg Pike, suite 200, Lancaster, PA 17604

We offer competitive pay as well as PTO, Holiday pay, and comprehensive benefits package!

• Health insurance
• Vision insurance
• Life Insurance
• Pet Insurance
• Health savings account
• Paid time off
• Paid holidays
• Profit sharing
• Free parking

GENERAL SUMMARY

Exciting opportunity to contribute to life-changing research while growing your career in a dynamic, supportive environment. Join our team as a Clinical Research Coordinator RN and play a vital role in cutting-edge clinical trials!

Clinical Research Coordinator, RN’s are primarily responsible for study coordination and data management, with a central focus on managing subject recruitment and enrollment, consistency of study implementation, data management and integrity, and compliance with regulatory requirements and reporting.

ESSENTIAL JOB FUNCTION/COMPETENCIES

The responsibilities and duties described in this job description are intended to provide a general overview of the position. Duties may vary depending on the specific needs of the affiliate or location you are working at and/or state requirements. Responsibilities include but are not limited to:

• Maintain site compliance for all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
• Maintain working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s).
• Complete all relevant Profound Research required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner.
• Educates and directs protocol compliance with physicians and staff.
• Assists in developing tools to meet requirements of new protocols.
• Manages protocols with increased clinical complexities including translational investigator-initiated research as well as multi center trials.
• Ensure good documentation practices are applied by all team members when collecting, maintaining, and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
• Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
• Acts as a patient advocate by providing education to and responding to questions from patients about protocols.
• Works with patients to ensure adherence with the protocol.
• Collaborates with scheduling staff to assure that future appointments for the patients (follow up visits and diagnostic testing) are scheduled correctly and timely.
• Collaborates with the physician to assure orders for treatment are written per protocol and delivered at the prescribed protocol intervals.
• Performs other position related duties as assigned.
• Employees shall adhere to high standards of ethical conduct and will comply with and assist in complying with all applicable laws and regulations. This will include and not be limited to following the Solaris Health Code of Conduct and all Solaris Health and Affiliated Practice policies and procedures; maintaining the confidentiality of patients' protected health information in compliance with the Health Insurance Portability and Accountability Act (HIPAA); immediately reporting any suspected concerns and/or violations to a supervisor and/or the Compliance Department; and the timely completion the Annual Compliance Training.

CERTIFICATIONS, LICENSURES OR REGISTRY REQUIREMENTS

• BLS certification required, ACLS preferred.
• RN licensure and certifications as required by State.
• Clinical research certification from SoCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals) preferred.

KNOWLEDGE | SKILLS | ABILITIES

• Ability to Start IVs and Administer IV medications
• Ability to draw blood
• Understanding of all aspects of biomedical research protocols, ensuring applicable regulations, and guidelines.
• Maintains patient confidentially.
• Excellent verbal and written communication skills.
• Skill in using computer programs and applications.
• Maintains current knowledge and awareness of organizational and regulatory standards, policies and procedures.
• Excellent organizational skills and attention to detail.
• Ability to build relationships with patients and display empathy and compassion to patients
• Skill in using computer programs and applications including Microsoft Office.
• Complies with HIPAA regulations for patient confidentiality.
• Complies with all health and safety policies of the organization.

EDUCATION REQUIREMENTS

• Must be a Registered Nurse (RN) with a current and valid license. Associate’s or Bachelor’s degree in Nursing (ASN or BSN) required.

EXPERIENCE REQUIREMENTS

• 2 or more years Nursing experience in ICU, ER, oncology or clinical trial experience, preferred.

REQUIRED TRAVEL

• May require travel to other site locations in practice.
• May require travel to Investigator and other meetings.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research

• Industries

  Hospitals and Health Care

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Medical insurance

Vision insurance

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