Search jobs > Durham, NC > Clinical research coordinator

Clinical Research Coordinator - Psychiatry - Behavioral Medicine Division - Neascsiu Team

Duke Health
Durham, NC, US
Full-time

Clinical Research Coordinator - Psychiatry - Behavioral Medicine Division - Neascsiu Team

Work Arrangement : Requisition Number : 242108 Regular or Temporary : Regular Location :

Durham, NC, US, 27710

Personnel Area : MEDICAL CENTER Date : Jun 17, 2024

School of Medicine

Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe.

Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center.

The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.

Operations : (25%)

Knowledgeable in regulatory and institutional policies and processes; applies appropriately in study documentation, protocol submissions, and SOPs.

May train others in these policies and processes. Prepares for and provides support for study monitoring and audit visits, including support for the reviewer.

Addresses and corrects findings. May train others. Maintains participant level documentation for all studies, including those that are complex in nature (e.

g., procedural and interventional studies) and / or require access to the Duke EHR. May train or oversee others. Employ strategies to maintain retention rates.

Evaluate processes to identify problems with retention. May train or oversee others. Employs and may develop strategies to maintain recruitment rates and evaluate processes to identify problems.

Escalates issues. May train or oversee others. Screens participants for complex studies (e.g., procedural and interventional studies).

May train or oversee others. Develops or helps develop SOPs. May train or oversee others. Independently employs simple procedures for collecting, preparing, processing, shipping, and maintaining inventory of specimens.

Assists with establishing and maintaining study level documentation. Conducts activities for study visits in compliance with the protocol.

May train staff. Participates in study team meetings.

Ethics : (5%)

Identifies all AEs, and determines whether or not they are reportable. Collaborates with the PI to determine AE attributes, including relatedness to study.

May train or oversee others. Conducts and documents consent for participants for all types of studies, including those that are complex in nature and / or require any orders in Maestro Care.

May train or oversee others.

Data : (30%)

Under direct supervision from Biostatistician and PI may perform basic analyses on structured data. Enters and collects basic data for research studies.

May score scripted or validated tests and measures. With supervision, responds to queries created by a CRO or the data manager.

May assists with quality control and data cleaning as directed. Independently corrects and documents incomplete, inaccurate or missing data for non-complex studies.

Follows SOPs for quality assurance. Runs summaries and reports on existing data. Follows required processes, policies, and systems to ensure data security and provenance.

In addition, recognizes and reports security of physical and electronic data vulnerabilities. Knowledgeable about the use of data standard policies.

Learns and uses new technology when required. Assists in updating reports on study progress for the PI and other study team members and collaborators.

Under supervision, executes predetermined testing scripts after the completion of a build, or following any project changes or system upgrades.

Science : (5%)

Assists with or contributes to the development of funding proposals. Assists with simple literature searches. Demonstrates a basic understanding of the elements of research study designs.

Contributes to the development of scientific publications or presentations. Serves as an author on poster presentations or publications.

Study and Site Management : (30%)

As directed, attends or schedules site visits. Uses clinical research management system and its reports to manage research participants' activities, calendars, tracking / marking financial milestones, and all aspects of study visits.

Uses required EMR functionalities to manage participants and study visits. May train others. For studies with simple supplies or equipment, ensures that there are ample supplies and that equipment is in good working order.

Ensure that studies are conducted in compliance with institutional requirements and other policies. Follows protocol-specific systems and process flows.

As directed, assists in preparing studies for closeout, (e.g., packing files, documenting files for storage, shipping extra supplies back to sponsor).

Leadership : (5%)

Maintains Duke and project specific training requirements. Keeps current with research updates by attending key external departmental meetings (i.

e. Research Wednesday, RPN, additional training, etc.). Navigates processes and people involved in Duke clinical research, demonstrates organizational awareness, and has the interpersonal skills necessary to get work done efficiently.

Demonstrates resilience and is adaptive to change. Uses advanced subject matter expertise in the therapeutic area or clinical research to solve problems.

Communicates effectively with others, regardless of reporting relationship, to accomplish shared work objectives.

Type of Research :

Conduct screening and neurostimulation visits with clinical adult participants.

Special skills :

Prior experience with neurostimulation / neuromodulation / TMS / TDCS / TBS / TACS is a plus.

Minimum Qualifications

Education

Completion of an Associate's degree

Experience

Work requires a minimum of two years of relevant research experience. A Bachelor's degree may substitute for 2 years required experience.

Duke is an Affirmative Action / Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, sexual orientation, or veteran status.

Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes.

To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard.

All members of our community have a responsibility to uphold these values.

Essential Physical Job Functions : Certain jobsat Duke University and Duke University Health System may include essential job functions that require specific physical and / or mental abilities.

Additional information and provision for requests for reasonable accommodation will be provided by each hiring department.

Nearest Major Market : Durham

Nearest Secondary Market : Raleigh

30+ days ago
Related jobs
Promoted
Wake Research
Durham, North Carolina

M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). As a Clinical Research Physician, you will provide ...

Promoted
UNC Health Care
Chapel Hill, North Carolina

In addition to demonstrating clinical leadership on the unit, the Clinical Nurse IV serves as a resource and system-wide consultant to staff and participates in endeavors to increase nursing knowledge. As part of our career ladder, the Clinical Nurse IV applicant should provide evidence of clinical ...

Promoted
Duke University
Durham, North Carolina

Provide leadership for a clinical team that conducts multiple, complex oncology clinical trials and research studies including Investigational Products [IP] for the Duke Cancer Institute's [DCI] Breast Clinical Research Program [BRST]. The Oncology Clinical Research Unit [CRU] oversees the conduct o...

Promoted
UNC Health Care
Chapel Hill, North Carolina

The Clinical Research Nurse Coordinator is responsible for independently providing specialized nursing services for various clinical research protocols. They are responsible for providing guidance and assistance to study teams in both clinical and non-clinical areas of research, including participan...

WakeMed
Raleigh, North Carolina

Certified Clinical Research Coordinator Or Certified Clinical Research Professional Preferred. Assist the Investigators and research team with the planning and implementation of clinical trials including the ?Growing Together? clinical study with pediatric primary care. Conduct the trial-required ho...

Promoted
UNC Health Care
Raleigh, North Carolina

RESEARCH AND PERFORMANCE IMPROVEMENT - Collaborates with Nurse Manager to evaluate research that is applicable to practice and promotes changes in standards of care as appropriate. Utilizes resources in asking research questions and applying appropriate research methods. UNC Health REX Cardiac Medic...

HERC- Southeast
Chapel Hill, North Carolina

The Clinical Research Regulatory Coordinator is responsible for research regulatory management for a variety of complex clinical research protocols, including leading efforts in gathering, editing, compiling, and reporting regulatory information. This position will serve as a Clinical Research Regul...

Duke Health
Durham, North Carolina

MiSTiC) in the Oncology Clinical Research Unit, which oversees the conduct of DCI clinical research. Clinical Research Coordinator. Summarize and clarify for study teams the professional guidelines and code of ethics related to the conduct of clinical research. Job Code: 00001201 CLINICAL RESEARCH C...

Medix
Raleigh, North Carolina

We are looking to add a CRC to our growing team- if you enjoy a collaborative environment and are looking for a company with a ton of room for growth- join our team! We are looking for someone interested in moving into a leadership role in the next 12 months. Knowledge and understanding of Federal r...

New Leaf Behavioral Health
Raleigh, North Carolina

We seek a creative and talented individual to join our team in an administrative capacity. Enjoying working on a team, and possessing a positive attitude. About New Leaf Behavioral Health:. New Leaf Behavioral Health is a 501(c)3 non-profit community mental health organization founded to ensure that...