Clinical Research Coordinator I

Eastern Nephrology Associates (ENA); Wilmington (NC); On-site; USD 32,000 - 36,000; Full time

Job summary

Eastern Nephrology Associates seeks a Clinical Research Coordinator I to support onsite clinical trials in Wilmington, NC. The role focuses on coordinating study activities, ensuring data accuracy, and maintaining regulatory documentation under PI supervision.

The position is patient-facing and requires in-person collaboration with providers and accurate handling of sensitive health information in strict HIPAA compliance. Prior CRP/clinical research experience is preferred.

Qualifications

• 2 to 4 years of healthcare experience or 2 to 4 years as a Clinical Research Assistant, or any combination of the two.
• Certified Medical Assistant required.
• Maintains confidentiality and HIPAA compliance.

Responsibilities

• Coordinate all aspects of clinical research activities for assigned studies at investigative site.
• Ensure data accuracy and timely collection for study timelines and protocol.
• Prepare and submit regulatory documents; perform study-specific procedures per Principal Investigator guidance.
• Maintain essential study documentation and ensure compliance with GCP, ICH, and FDA guidelines.

Skills

Healthcare experience

Certified Medical Assistant

Communication skills

On-call readiness

Tools

Microsoft Office

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Clinical Research Coordinator I

Full Time Technical Wilmington, NC, US

3 days ago Requisition ID: 1166

Salary Range: $22.48 To $26.44 Hourly

Summary

To serve as a clinical research coordinator during the conduct of clinical research at the investigative site. Works under the direct supervision of the Principal Investigator. Coordinates all activities for the implementation and conduct of clinical trials. Responsible for the collection, accuracy, and validity of data for assigned clinical studies in accordance with the study protocol and study timelines. Responsible for the collection and submission of regulatory documents, performance of study specific procedures and regulatory reporting requirements as instructed by the Principal Investigator and governed by Good Clinical Practice and International Council for Harmonization. Works under the supervision of the Principal Investigator to conceptually apply research protocol to clinical setting to allow for accurate and timely completion of all duties. Maintains all appropriate documentation associated with the assigned clinical study. Ensures studies are conducted according to established organization policies and procedures as well as all applicable State and Federal regulations, specifically Good Clinical Practice, International Council for Harmonization and Food and Drug Administration guidelines.

This position is designated as an on-site, patient-facing role. In-office presence is an essential function due to the need for real-time collaboration with providers, direct interaction with patients and caregivers, and secure handling of health data in compliance with HIPAA.

Qualification Requirements

• 2 to 4 years of healthcare experience or 2 to 4 years as a Clinical Research Assistant, or any combination of the two.
• Certified Medical Assistant Required.
• Healthcare and/or Research experience preferred.
• Skilled in the use of personal computers and related software applications to include Microsoft Office Applications and email.
• Participates in 24-hour emergency on-call rotation
• Valid drivers’ license and reliable transportation to allow individual to provide support to offsite locations, as necessary.
• Ability to provide a minimum of a 4 week notice in the event resignation is tendered.

Knowledge, Skills, and Abilities

• Excellent record maintenance skills.
• Ability to communicate effectively both orally and written.
• Proactive individual with the ability to be a self-starter with
• Maintain a positive and professional attitude in all aspects of work from patient care to interaction with co-workers and physicians.
• Demonstrated human relations and effective communication skills are required.
• Ability to understand the ethics of confidentiality and the ability to maintain confidentiality of sensitive information.
• Willing to pursue research certification when eligible.
• Maintains confidentiality of patients and their medical information.
• Maintains confidentiality of research activities as required by study sponsor confidentiality agreements and mandates.
• Must be able to meet deadlines for multiple concurrent projects.
• Ability to understand and follow policies, procedures and direction.
• Ability to foster a cooperative work environment. Possess willingness to accept orders and to perform repetitive tasks.
• Strong interpersonal and communication skills and the ability to work effectively with a wide range of constituencies in a diverse community.
• Ability to make evaluative judgments.
• Ability to function well while involved in multiple task assignments.
• Ability to concentrate on details and deal with constant interruption.
• Skill in organizing resources and establishing priorities.
• Ability to travel to attend off-site meetings as necessary and directed.
• Ability to delegate tasks to clinical research assistants and clinical research administrative assistants as applicable.
• Ability to ensure studies are conducted according to established organization policies and procedures as well as all applicable State and Federal regulations, specifically Good Clinical Practice, International Council for Harmonization and Food and Drug Administration guidelines.

Ability to function independently and enjoy a fast paced, challenging, changing environment; possesses the energy and commitment to help the organization move forward.

Supervisory Responsibilities: None

Essential Functions (%)

• ENA has determined that these duties cannot be effectively or securely executed in a remote environment without compromising patient care, data privacy, or operational standards.
• Coordinate all aspects of clinical research activities for assigned studies at investigative site- 90%
• Other duties as assigned -10%

Physical Demands

• The employee may be required to assist in patient transfer and should use appropriate techniques and equipment to safely transfer patients.
• Hearing, visual acuity, depth perception, balancing, handling, and talking and requires full range of body motion.
• Reaching, grabbing, holding – fine motor skills with dexterity and eye-hand coordination
• Extended periods in a stationary or standing position
• Repetitive motion such as entering data into computer-based programs
• Lift or move up to 30 pounds. Employees are expected to use appropriate ergonomics and tools such as hand carts for heavier loads.
• Work is normally performed in a typical interior/office work environment.
• The noise level is usually moderate.
• This position requires visual acuity eyesight (corrected or uncorrected).
• Moderate risk of exposure to blood borne pathogens and OPIM.

The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties and skills required for the position. All employees may have other duties assigned at any time.

This position falls under a 180- day evaluation review period.

This position is designated as an on-site, patient-facing role. In-office presence is an essential function due to the need for real-time collaboration with providers, direct interaction with patients and caregivers, and secure handling of health data in compliance with HIPAA.

To request a reasonable accommodation for any part of the application or hiring process, please see our Accessibility Statement or contact Human Resources at [e-mail] or 252-864-2049.