FULL_TIME

FEED

UNKNOWN

Responsibilities: Our client is looking for Full Time Nurse Educator with Perioperative Services OR AND RN Education who will be responsible for: Needs assessment, planning, intervention and evaluation of educational experiences for staff utilizing an interdisciplinary approach. As a gesture of appreciation for your referral, you will receive a 5% referral amount of the yearly salary of your referred candidate once they are hired by our client.

Responsibilities: Our client is looking for Full Time Nurse Educator with Perioperative Services OR AND RN Education who will be responsible for: Needs assessment, planning, intervention and evaluation of educational experiences for staff utilizing an interdisciplinary approach. Developing and maintaining methods to ensure staff competency consistent with regulatory agency requirements. Facilitating the orientee's successful integration into the unit-based healthcare team. Developing clinical practice skills based upon current trends and research findings. Development, review, and revision of clinical policies, procedures, and standards. Serving as a role model and is recognized for clinical expertise in the hospital and community setting. Qualifications: Bachelor of Science in Nursing. MSN Preferred. PA Registered Nurse License. BLS via AHA Required. CNOR Preferred. Required Skills: Change Management. Customer Service Skills. Excellent Interpersonal Skill. Refer Talent, Earn Rewards: Your Network, Your Reward!! We encourage you to refer friends and colleagues who may be a good fit for this role. As a gesture of appreciation for your referral, you will receive a 5% referral amount of the yearly salary of your referred candidate once they are hired by our client. This referral amount will be granted to you upon the completion of 120 days in their new position at our client.

Macpower Digital Assets Edge LLC

Full Time Nurse Educator

Change Management

Clinical Competency

Customer Support/Service

Educational Evaluation

Healthcare

Hospital

Interpersonal Skills

Needs Assessment

Nursing

Perioperative Nursing

Registered Nurse (RN)

Regulatory Requirements

Training/Teaching

Trend Analysis

YEAR

This role works directly with principal investigators, study teams, and enrolled participants to ensure protocol adherence and data integrity throughout each trial's lifecycle. The Clinical Research Coordinator will manage day-to-day study operations including participant recruitment and scheduling, regulatory document maintenance, and adverse event tracking.

<p>Our client, a pharmaceutical company based in Philadelphia, is seeking a Clinical Research Coordinator to support ongoing clinical trials across multiple therapeutic areas. This role works directly with principal investigators, study teams, and enrolled participants to ensure protocol adherence and data integrity throughout each trial's lifecycle.</p><p>The Clinical Research Coordinator will manage day-to-day study operations including participant recruitment and scheduling, regulatory document maintenance, and adverse event tracking. The position operates within a collaborative, fast-paced research environment and requires strong attention to detail and a working knowledge of ICH/GCP guidelines.</p><p>This is a full-time, on-site position located in Philadelphia's University City research corridor. The organization provides structured onboarding, ongoing GCP training reimbursement, and exposure to a diverse pipeline of studies spanning Phase I through Phase III trials.</p><h3>Responsibilities</h3><ul><li>Coordinate patient recruitment, screening, and enrollment for assigned clinical studies</li><li>Maintain regulatory binders and study documentation in compliance with ICH/GCP standards</li><li>Schedule and conduct study visits, collecting participant data and biological samples per protocol</li><li>Enter and verify data in electronic data capture systems such as REDCap or Medidata Rave</li><li>Communicate with IRBs, sponsors, and clinical monitors regarding regulatory requirements and protocol updates</li><li>Track, document, and report adverse events and protocol deviations to the principal investigator</li><li>Support site initiation activities including staff training and document preparation</li><li>Assist with study closeout tasks including final data reconciliation and archival</li></ul><h3>Requirements</h3><ul><li>Bachelor's degree in life sciences, health sciences, nursing, or a related field</li><li>Minimum 2 years of experience in clinical research coordination or a comparable clinical role</li><li>Familiarity with FDA regulations and ICH/GCP guidelines governing clinical trial conduct</li><li>Hands-on experience with at least one electronic data capture platform</li><li>Strong organizational skills with the ability to manage multiple concurrent active studies</li><li>Clear written and verbal communication skills for working with participants, sponsors, and research staff</li><li>CCRP or CCRC certification preferred, or willingness to obtain within 12 months of hire</li><li>Ability to work on-site in Philadelphia five days per week</li></ul><h3>Benefits</h3><ul><li>Competitive base salary with annual merit review</li><li>Medical, dental, and vision insurance effective on start date</li><li>401(k) plan with employer matching contributions</li><li>GCP certification and continuing education reimbursement</li><li>Paid vacation, sick leave, and 10 company-observed holidays</li><li>Flexible scheduling within established core research hours</li><li>Clear promotion pathway to Senior CRC or Study Manager roles</li></ul>

Full Time Research Jobs in Hamilton, NJ

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Full Time Research Jobs in Hamilton, NJ

Full Time Nurse Educator Macpower Digital Assets Edge LLC

Clinical Research Coordinator Careerscape

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