Clinical Study Nurse Coordinator Jobs in Union, Arkansas

Act with integrity in everything we do.

Develop superior talent and deliver expertise.

Respond with agility and provide timely results.

Embrace collaboration, diverse perspectives and ideas.

Come and work for an organization with the:

Note that vendor management is not limited to the CRO, but includes ancillary vendors (e.g. translations, trial insurance, and central laboratory).

Ensure DS internal tracking systems are updated (e.g. Global Project Management System, GPMS).

Education Qualifications (from An Accredited College Or University)

Associate degree or with a nursing diploma with substantial experience preferred.

4 or More Years relevant experience is required with a BS preferred.

Bachelor's Degree in the Sciences preferred.

Oversee data collection, management, and entry into study databases, ensuring accuracy and completeness

Strong knowledge of clinical research processes, regulations, and guidelines.

Excellent organizational, communication, and interpersonal skills.

Collaborate with study teams to develop and implement study protocols, ensuring compliance with regulatory guidelines and ethical considerations

Coordinate participant recruitment and enrollment activities, including screening, selection, and informed consent processes

BA/BS degree in a relevant subject

Co-manages maintenance of the centralized Informed Consent Form mailbox.

Minimum of three years of relevant experience in the biopharmaceutical/CRO industry.

Ability to manage multiple tasks simultaneously and meet deliverables in accordance with stated timelines.

MUST CURRENTLY WORK AT A CRO/PHARMA

Reviews and validates quality and accuracy of Informed Consent Form templates.

Supports development of Informed Consent Form templates.

Management experience of CROs, Vendors and Consultants preferred

Ensures the competencies and skills required for the Clinical team is consistent with the company defined requirements

Mentor junior team members to support development by delegating responsibilities, overseeing and supporting development plans

8+ years progressive experience in clinical operations preferably within the biotech, pharmaceutical, and/or CRO environment

Possess understanding of treatment landscape, standard of care, upcoming approvals, and good knowledge of KOLs and investigators

Experience developing trial plans including site monitoring, pharmacy and lab manuals, risk mitigation strategies, trial budgets and site selection/feasibility as required

Support the organization with daily tasks including user management, site management, equipment requests, data entry and report generation

Provide support for front-end client activities across multiple clinical research studies

Work closely with clients to ensure all data required for study start-up is collected and maintained

Provide details and information to clients in response to inquiries regarding study support and set-up

Update project-related internal databases and electronic files to ensure accuracy

Assist with special department projects

Must have excellent management and communication skills (written and verbal), strong problem-solving skills, and be detail oriented

Manages vendors, including the implementation and coordination of vendor’s Scope of Work (SOW).

Manages study budget and timelines. Identifies, resolves, or escalates issues involving study timelines and deliverables

Relevant experience as a CRA preferred

Study planning and set-up, maintenance, and close-out experience.

Must have a solid understanding of clinical research operations including GCP and regulatory requirements and operational procedures

Minimum of 3-5 years of project management experience in the pharmaceutical industry, with a focus on clinical study management

PMP or similar project management certification is preferred

Collaborate with cross-functional teams, including clinical operations, data management, biostatistics, and quality assurance, to ensure seamless study execution

Familiarity with Veeva or other relevant clinical trial management systems

Veeva or similar study management platform

Study Project Manager - 100% remote

Run reports including training matrix reports, metrics for management reviews

Support management of IRB/IEC renewal compliance.

Work with management group to help achieve department goals.

Requires experience and knowledge working with computer systems (Microsoft office –

Assist in payments/tracking for patient reimbursements. Performs data entry in systems

Is responsible for ensuring appropriate level of communication with managers, project leaders, and team members.

Education assistance (tuition, student loan, certification support, dependent scholarships)

Learn More About The Benefits Offered For This Job.

Family support through fertility and family building benefits with Progyny and adoption assistance.

Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.

Collaborates with subject matter experts and other managers to create an environment of teamwork that supports improved outcomes and service.

Assists with staff scheduling. Manages all practical aspects of staff labor in accordance with patient care needs and established productivity guidelines.

Bachelor's Degree required, or equivalent combination of education and related experience.

Adheres to Good Clinical Practice, regulatory, and grant agency requirements

Collects, labels, logs, processes, and ships biological specimens for analysis according to protocol and training requirements

1-3 years of relevant experience, required.

Completes the activities assigned to the Clinical Research Coordinator by local research team and ECHO program leadership

Maintains comprehensive study documents/records as requested by ECHO program core elements, regulatory agencies, the NIH, and local study leadership

Minimum 6 years or successful execution of over 30 clinical trial studies or collaborative biomedical laboratory study experience (Study Coordinator II)

Preferred experience in managing investigator-initiated, industry-sponsored, or military studies.

Ability to analyze data and summarize findings for incorporation into reports.

The Contractor shall match sponsored studies with appropriate Principal Investigator.

The Contractor shall assure that logs and collected data from patients enrolled in the study remain confidential.

Must have a Bachelors of Science in biomedical science field or nursing

BLS certification from the American Heart Association required

3 years' or more experience in nursing

Provides education concerning various aspects of the care

Coordinates initial education of patients by phone

RN License by Texas Board of Nursing or Nurse Licensure Compac

Responsible and accountable for the daily care coordination of patients within area of clinical

Required Additional Knowledge, Skills and Abilities:

Preferred Additional Knowledge, Skills and Abilities:

If any experience is required, please specify what kind of experience:

If yes, what is the required licensure/certification?

Nursing experience in oncology and/or clinical research.

If yes, what is the preferred licensure/certification?:

Familiarity and comfort with Database management, Word, Access and Excel will be necessary to meet job needs

MA Licensure as an RN. Clinical research experience preferred;

Computer and Internet skills required;

Understanding of regulations and requirements related to nursing practice and research protocols;

The research nurse will have frequent telephone communication with subjects and must be skilled at communicating and obtaining necessary information;

Good interpersonal and communication skills;

Bachelor’s Degree in business administration, finance, science or related field or equivalent experience.

Central Services Specialist - ICF Management

Co-manages maintenance of the centralized Informed Consent Form mailbox.

Minimum of three years of relevant experience in the biopharmaceutical/CRO industry.

Experience in negotiating vendor contracts/budgets.

Proven ability to effectively manage change.

Analyzes protocol specific requirements and implements quality assurance measures to ensure physician, patient, and clinician compliance.

Three (3) years of related experience required.

Organizational, analytical, and problem-solving skills required.

Demonstrated verbal and written skills at professional level required.

CERTIFICATIONS/LICENSURES REQUIRED: SOCRA or ACRP certification required.

education and training, the health system has trained nearly 40% of physicians currently practicing

Skills / Knowledge / Abilities

Does this position have supervisory responsibilities?

Nurse Coordinator Clinical/ENT Service Line

Relevant administrative experience including detail oriented, collaborative, positive attitude, ability to prioritize, proactive, and good follow up skills,

Administrative tasks and activities may be requested by a line manager, study team member, or GSO department staff.

Assist with tracking and review of Clinical Trial Insurance requirements, expiry dates, insurance renewal, certificate distribution, and archival

Activities and responsibilities may include:

The SS I is not allocated as a resource to any specific study or program.

BOARD Quarterly MVR GSO Compliance and other metrics

currently conducting several trials and are seeking an experienced Assistant Study Coordinator.

Attending site qualification and initiation visits

280 Washington St, Suite 204

MetroBoston Clinical Partners is a growing research organization with two offices in the

metro Boston area. We have a friendly staff and a great work environment. We are

Assistant Study Coordinator part time