Current jobs related to Clinical Research Coordinator - Nutley - Hackensack Meridian Health


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    OverviewAt Hackensack Meridian Health, our team members are the foundation of our success. We are dedicated to helping our patients lead healthier lives while fostering an environment where our employees can thrive. Our culture emphasizes connection and collaboration, where competitive benefits are just the starting point. It's about mutual support and...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    Position Overview:At Hackensack Meridian Health, our team members are integral to our mission of enhancing patient care and fostering a supportive work environment. We believe in a culture that emphasizes teamwork and collaboration, where competitive benefits are just the beginning of our commitment to each other and our community.As a Clinical Trials...


  • Nutley, United States Maxis Clinical Sciences Full time

    Job DescriptionJob Descriptionob Title:Senior SAS Programmer with RMust have some application development work (R, SAS macros,python, VB skills) along with study work.Duties:Under moderate guidance, designs, develops, evaluates and modifies SAS programs to analyze and evaluate clinical data.Plans, writes and executes statistical programs designed to analyze...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    OverviewThe Research Assistant, CPC will be responsible for the day-to-day completion of tasks necessary for the success of an assigned behavioral science research project or set of related projects performed by or in conjunction with the Cancer Prevention and Control Program of Hackensack University Medical Center/John Theurer Cancer Center.The Center for...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    Position OverviewAt Hackensack Meridian Health, our dedicated team members are the foundation of our success. We are committed to enhancing the health and well-being of our patients while fostering a supportive environment for our employees. Our culture emphasizes collaboration and connection, ensuring that competitive benefits are just the beginning of what...


  • Nutley, United States Hackensack Meridian Health Full time

    Overview The Research Assistant, CPC will be responsible for the day-to-day completion of tasks necessary for the success of an assigned behavioral science research project or set of related projects performed by or in conjunction with the Cancer Prevention and Control Program of Hackensack University Medical Center/John Theurer Cancer Center. The Center for...


  • Nutley, New Jersey, United States LHC Group Full time

    Position OverviewThe Home Health Care Manager plays a pivotal role in overseeing and coordinating clinical services within the organization. This position is essential for ensuring that patients receive high-quality care in their homes.Key ResponsibilitiesSupervise an interdisciplinary team to guarantee the delivery of comprehensive care to home health...

  • RN Clinical Manager

    4 days ago


    Nutley, United States Patient Care Full time

    Job DescriptionThe Home Health Patient Care Manager is responsible for the overall supervision and coordination of clinical services. Coordinates and supervises an interdisciplinary team of staff to assure the continuity of high quality care to home health patients assigned to the team's area in accordance with physician prescribed plan of care, and all...

  • RN Clinical Manager

    5 days ago


    Nutley, United States Patient Care Full time

    Job DescriptionThe Home Health Patient Care Manager is responsible for the overall supervision and coordination of clinical services. Coordinates and supervises an interdisciplinary team of staff to assure the continuity of high quality care to home health patients assigned to the team's area in accordance with physician prescribed plan of care, and all...

  • Research Director

    2 days ago


    Nutley, New Jersey, United States Hackensack Meridian Health Full time

    About the RoleWe are seeking a highly experienced and accomplished Research Director to join our team at Hackensack Meridian Health. As a key member of our leadership team, you will play a critical role in driving our research agenda and advancing our mission to improve patient outcomes.Key ResponsibilitiesLeadership and StrategyDevelop and implement short...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    The Animal Care Technician will deliver essential support for laboratory animals and provide technical assistance to the veterinary team and researchers at the Animal Facility within Hackensack Meridian Health.Hackensack Meridian Health has established a robust research environment aimed at advancing scientific innovations to clinical applications,...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    About the RoleWe are seeking a highly qualified Professor of Medical Sciences to join our team at Hackensack Meridian Health. As a Professor, you will play a pivotal role in shaping the next generation of physicians through innovative education and groundbreaking research.Key ResponsibilitiesCurriculum Development: Design and deliver dynamic 3+1 curriculum,...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    About the RoleWe are seeking a highly qualified Professor of Medical Sciences to join our team at Hackensack Meridian Health. As a Professor, you will play a pivotal role in shaping the next generation of physicians through innovative education and groundbreaking research.Key ResponsibilitiesCurriculum Development: Participate in the design and delivery of...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    Position Overview At Hackensack Meridian Health, our workforce is the cornerstone of our success. We are dedicated to enhancing the well-being of our patients while fostering an environment where our team members can thrive. Our culture emphasizes collaboration and connection, ensuring that our employees are valued contributors. Competitive benefits are just...


  • Nutley, United States Patient Care Full time

    The Home Health Patient Care Manager is responsible for the overall supervision and coordination of clinical services. Coordinates and supervises an interdisciplinary team of staff to assure the continuity of high quality care to home health patients assigned to the team's area in accordance with physician prescribed plan of care, and all applicable state...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    At Hackensack Meridian Health, our team members are the foundation of our success. We are dedicated to helping our patients lead healthier lives while fostering an environment where our employees can thrive. Our culture emphasizes connection and collaboration, ensuring that our team members feel valued. Competitive benefits are just the beginning; we...


  • Nutley, United States LHC Group Full time

    SummaryThe Home Health Patient Care Manager is responsible for the overall supervision and coordination of clinical services. Coordinates and supervises an interdisciplinary team of staff to assure the continuity of high quality care to home health patients assigned to the team's area in accordance with physician prescribed plan of care, and all applicable...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    About the RoleHackensack Meridian Health is seeking a highly qualified Medical Sciences Professor to join our team. As a key member of our faculty, you will play a vital role in shaping the educational experience of our students.Key ResponsibilitiesDevelop and implement innovative curricula in histology, cytology, anatomy, and pathology for our pre-clerkship...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    Position OverviewAt Hackensack Meridian Health, our team members are essential to our mission of enhancing the health and well-being of our patients. We foster a culture of collaboration and connection, ensuring that our employees feel valued and supported. Our competitive benefits are just the beginning; we prioritize teamwork and community engagement.As an...


  • Nutley, New Jersey, United States Hackensack Meridian Health Full time

    About the RoleHackensack Meridian Health is seeking a highly qualified Medical Sciences Professor to join our team. As a key member of our faculty, you will play a vital role in shaping the educational experience of our students.Key ResponsibilitiesDevelop and implement innovative curricula in histology, cytology, anatomy, and pathology for our pre-clerkship...

Clinical Research Coordinator

2 months ago


Nutley, United States Hackensack Meridian Health Full time

Overview

Our team members are the heart of what makes us better.

At Hackensack Meridian Health we help our patients live better, healthier lives - and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. It's also about how we support one another and how we show up for our community.

Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader of positive change.

The Clinical Research Coordinator is responsible for coordinating and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning, implementing and compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries out the research and works under the general supervision of the principal investigator responsible for the clinical trial(s) to which is assigned.

Responsibilities

A day in the life of a Clinical Research Coordinator at Hackensack Meridian Health includes:

  • Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol.
  • In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
  • Reviews study with principal investigator and/or clinical research nurses to a budget outlining standard of care and research costs. Finalizes budget draft with budget coordinator.
  • Reviews proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks. Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
  • Coordinates research activities not limited to: scheduling laboratory tests, radiology testing and other medical exams as required.
  • Works with the study team to draft/create study specific study orders, billing templates and study calendars as necessary.
  • Schedules subjects for appointments, procedures, or inpatient stays as required by study protocols.
  • Monitors all study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional policies.
  • Registers protocol patients with appropriate statistical centers as required.
  • Tracks enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
  • Acts as principal investigators representative as appropriate. This may include communicating with sponsors and their representatives, the IRB and other medical personnel.
  • Along with clinical research nurses, maintains accurate, complete, up-to-date records on each protocol and each patient participating in a clinical trial protocol in the clinical trial management system and all other systems as required.
  • Works closely with clinical research finance to ensure study patient's clinical trial related activities are billed appropriately.
  • Schedules, coordinates, prepares, and assists for all sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit; Meets with monitor at least once during each monitor site visit and resolves all issues found during visit.
  • Maintains contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
  • Ensures compliant maintenance of all required records of study activity including case report forms, drug dispensation records, or regulatory forms.
  • Oversees and directs the requisition, collection, labeling, storage, or shipment of specimens.
  • Prepares for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Prepares study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
  • Identifies protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions.
  • Organizes space for study equipment and supplies.
  • Participates in the development of study protocols including guidelines for administration or data collection procedures.
  • Contacts outside health care providers and communicate with subjects to obtain follow-up information.
  • Reviews scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.
  • Collaborates with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
  • Attends research meetings and conferences as required.
  • Participates in staff meetings and in-service education as necessary.
  • Other duties and/or projects as assigned.
  • Adheres to HMH Organizational competencies and standard of behavior.

Qualifications

Education, Knowledge, Skills and Abilities Required:

  • BA/BS diploma/degree in science or healthcare field.
  • Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field of clinical research.
  • Strong attention to detail and customer service focus.
  • Ability to work independently, or in a team, and handle multiple deadline driven tasks in a dynamic environment is essential.
  • Excellent organizational, presentation, documentation and interpersonal skills.
  • Excellent written and verbal communication skills.
  • Proficient computer skills that include but are not limited to Microsoft Office and/or Google Suite platforms.

Education, Knowledge, Skills and Abilities Preferred:

  • Education on human subject research and GCP.

Licenses and Certifications Preferred:

  • SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC).

If you feel that the above description speaks directly to your strengths and capabilities, then please apply today

Our Network

Hackensack Meridian Health (HMH) is a Mandatory Influenza Vaccination Facility

As a courtesy to assist you in your job search, we would like to send your resume to other areas of our Hackensack Meridian Health network who may have current openings that fit your skills and experience.